Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0002 | 0/0 | 1451 | 59 | 30 | 13 | 11 | 1 | 4 | 9 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0003 | 0/0 | 1451 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0004 | 0/0 | 1451 | 7 | 1 | 2 | 3 | 0 | 1 | 3 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0005 | 0/0 | 1451 | 5 | 0 | 0 | 2 | 0 | 3 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0006 | 0/0 | 1451 | 4 | 2 | 1 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0007 | 0/0 | 1451 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0008 | 0/0 | 1451 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0009 | 0/0 | 1451 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0010 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0011 | 0/0 | 1451 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0012 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0013 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0014 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| a0015 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | MVSKR others(1446): Show |
chr3 | 10021437 | 10106932 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4353 | 128 | 27 | 32 | 40 | 6 | 21 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0001c0003 | 0/0 | 4353 | 12 | 9 | 3 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0001c0011 | 0/0 | 4353 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0001c0016 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0001c0019 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0001c0023 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0002c0002 | 0/0 | 4353 | 56 | 30 | 10 | 11 | 1 | 4 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0002c0012 | 0/0 | 4353 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0002c0020 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0003c0004 | 0/0 | 4353 | 9 | 9 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0004c0005 | 0/0 | 4353 | 7 | 1 | 2 | 3 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0005c0008 | 0/0 | 4353 | 3 | 0 | 0 | 2 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0005c0013 | 0/0 | 4353 | 2 | 0 | 0 | 0 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0006c0006 | 0/0 | 4353 | 4 | 2 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0007c0007 | 0/0 | 4353 | 3 | 3 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0008c0009 | 0/0 | 4353 | 2 | 0 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0009c0010 | 0/0 | 4353 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0010c0021 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0011c0017 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0012c0014 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0013c0015 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0014c0022 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
chr3 | 10021437 | 10106932 | ||
| a0015c0018 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | ATGGT others(4348): Show |
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 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0003 | 0/0 | 5095 | 25 | 17 | 3 | 4 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0004 | 0/1 | 5096 | 28 | 1 | 10 | 7 | 2 | 7 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0007 | 0/0 | 5097 | 2 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0008 | 0/0 | 5096 | 3 | 0 | 0 | 3 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0010 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0011 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0012 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0018 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0001c0001t0019 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0001c0003t0002 | 0/0 | 5096 | 11 | 8 | 3 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0003t0006 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0001c0011t0002 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0011t0003 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0001c0016t0003 | 0/0 | 5095 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0001c0019t0001 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0001c0023t0001 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0002c0002t0002 | 0/0 | 5096 | 39 | 27 | 9 | 2 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0002c0002t0005 | 0/0 | 5097 | 9 | 0 | 0 | 7 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0002c0002t0006 | 0/0 | 5095 | 5 | 3 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0002c0002t0009 | 0/0 | 5096 | 2 | 0 | 0 | 2 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0002c0002t0017 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0002c0012t0005 | 0/0 | 5097 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0002c0020t0002 | 0/0 | 5096 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0003c0004t0003 | 0/0 | 5095 | 9 | 9 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0004c0005t0001 | 0/0 | 5096 | 6 | 1 | 2 | 3 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0004c0005t0016 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0005c0008t0001 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0005c0008t0007 | 0/0 | 5097 | 2 | 0 | 0 | 2 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0005c0013t0001 | 0/0 | 5096 | 2 | 0 | 0 | 0 | 0 | 2 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0006c0006t0002 | 0/0 | 5096 | 2 | 0 | 1 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0006c0006t0014 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0006c0006t0015 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0007c0007t0003 | 0/0 | 5095 | 3 | 3 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0008c0009t0004 | 0/0 | 5096 | 2 | 0 | 1 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0009c0010t0003 | 0/0 | 5095 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5090): Show |
chr3 | 10021437 | 10106932 |
| a0010c0021t0005 | 0/0 | 5097 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0011c0017t0004 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0012c0014t0013 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0013c0015t0001 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| a0014c0022t0007 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5092): Show |
chr3 | 10021437 | 10106932 |
| a0015c0018t0004 | 0/0 | 5096 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | GGGAA others(5091): Show |
chr3 | 10021437 | 10106932 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 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 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| 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 |
| a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0103 | 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 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0133 | 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 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0047 | 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 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0004g0110 | 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 |
| a0001c0001t0007g0036 | 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 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0001t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0003t0002g0003 | 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 |
| a0001c0003t0002g0131 | 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 |
| a0001c0003t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0011t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0011t0003g0235 | 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 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0001c0023t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0202 | 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 |
| a0002c0002t0002g0204 | 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 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0211 | 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 |
| a0002c0002t0005g0214 | 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 |
| a0002c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0002t0017g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0012t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0012t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0002c0020t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0003c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 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 |
| a0004c0005t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0004c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0004c0005t0016g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0005c0008t0007g0024 | 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 |
| a0006c0006t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0006c0006t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0007c0007t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0008c0009t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0008c0009t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0009c0010t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0009c0010t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0010c0021t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0011c0017t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0012c0014t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0013c0015t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0014c0022t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| a0015c0018t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0089 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0046 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00408 | hp1 | a0002 | c0002 | t0005 | g0215 | 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 | g0033 | EAS | CHS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00558 | hp2 | a0005 | c0008 | t0007 | g0023 | 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 | g0059 | 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 | g0219 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG00741 | hp2 | a0010 | c0021 | t0005 | g0178 | 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 | g0198 | 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 | g0067 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0131 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0192 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01081 | hp2 | a0008 | c0009 | t0004 | g0002 | 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 | g0041 | 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 | g0039 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | 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 | g0025 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01257 | hp2 | a0002 | c0012 | t0005 | g0189 | 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 | g0190 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01358 | hp2 | a0002 | c0020 | t0002 | g0223 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | 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 | g0040 | EUR | IBS | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01884 | hp2 | a0002 | c0002 | t0006 | g0172 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01891 | hp1 | a0003 | c0004 | t0003 | g0160 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01934 | hp2 | a0001 | c0019 | t0001 | g0001 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01952 | hp1 | a0004 | c0005 | t0001 | g0165 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01975 | hp1 | a0004 | c0005 | t0001 | g0169 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0222 | 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 | g0054 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0236 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0234 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02257 | hp2 | a0003 | c0004 | t0003 | g0161 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02258 | hp2 | a0009 | c0010 | t0003 | g0154 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PEL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | KHV | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02572 | hp1 | a0001 | c0011 | t0002 | g0195 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02602 | hp2 | a0002 | c0002 | t0017 | g0174 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02615 | hp2 | a0003 | c0004 | t0003 | g0162 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02622 | hp1 | a0003 | c0004 | t0003 | g0156 | 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 | g0205 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0185 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0232 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0101 | 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 | a0011 | c0017 | t0004 | g0062 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02698 | hp2 | a0001 | c0023 | t0001 | g0027 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02717 | hp2 | a0006 | c0006 | t0014 | g0218 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0226 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02738 | hp2 | a0005 | c0008 | t0001 | g0022 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02809 | hp1 | a0003 | c0004 | t0003 | g0163 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02818 | hp1 | a0012 | c0014 | t0013 | g0150 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0201 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0188 | 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 | g0200 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0186 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0229 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02970 | hp1 | a0013 | c0015 | t0001 | g0035 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02976 | hp1 | a0003 | c0004 | t0003 | g0164 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0193 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0063 | 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 | g0182 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03098 | hp1 | a0003 | c0004 | t0003 | g0157 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03098 | hp2 | a0007 | c0007 | t0003 | g0152 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0129 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03195 | hp1 | a0007 | c0007 | t0003 | g0153 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0130 | 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 | g0170 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | 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 | g0043 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03516 | hp1 | a0003 | c0004 | t0003 | g0158 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ESN | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0050 | AFR | GWD | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0202 | 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 | g0235 | 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 | g0228 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0042 | 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 | g0045 | 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 | g0093 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | BEB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG04115 | hp1 | a0006 | c0006 | t0002 | g0217 | 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 | g0227 | 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 | g0048 | SAS | STU | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18522 | hp1 | a0006 | c0006 | t0015 | g0216 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18747 | hp1 | a0014 | c0022 | t0007 | g0021 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18906 | hp1 | a0007 | c0007 | t0003 | g0151 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18940 | hp1 | a0002 | c0002 | t0005 | g0173 | 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 | g0060 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18948 | hp1 | a0002 | c0002 | t0005 | g0209 | 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 | g0049 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18953 | hp1 | a0002 | c0002 | t0005 | g0177 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18956 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18957 | hp2 | a0002 | c0002 | t0009 | g0176 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18967 | hp1 | a0005 | c0008 | t0007 | g0024 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0083 | 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 | g0167 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0214 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18985 | hp1 | a0002 | c0002 | t0005 | g0211 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18986 | hp1 | a0004 | c0005 | t0001 | g0168 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18988 | hp1 | a0004 | c0005 | t0001 | g0171 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19012 | hp1 | a0015 | c0018 | t0004 | g0079 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19056 | hp1 | a0002 | c0002 | t0009 | g0212 | 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 | g0213 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | YRI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20129 | hp2 | a0009 | c0010 | t0003 | g0155 | AFR | ASW | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20805 | hp1 | a0002 | c0002 | t0006 | g0197 | EUR | TSI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0066 | EUR | TSI | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | GIH | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | 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 | g0149 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG03471 | hp2 | a0003 | c0004 | t0003 | g0159 | AFR | MSL | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | USA | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0166 | 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 | a0001 | c0001 | t0004 | g0026 | REF | REF | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0019 | REF | REF | FANCD2_chr3_10021437_10106932 | FANCD2 | chr3 | 10021437 | 10106932 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0012 | 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 | a0005 a0014 |
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 | a0012 | 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 | a0003 a0007 a0009 others(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 | a0010 | 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 | a0003 a0007 |
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 | a0014 | 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 | a0002 a0006 a0010 |
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 | a0015 | 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 | a0011 | 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 | a0013 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0013c0015 | 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 | a0001c0011 a0002c0002 a0002c0012 others(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 | a0001c0011 a0002c0002 a0002c0012 others(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 | a0003c0004 a0007c0007 a0009c0010 |
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 | a0003c0004 a0007c0007 a0009c0010 others(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 | a0001c0003 a0001c0011 a0002c0002 others(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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10028652 | G | C | 3 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0011 |
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 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(5): Show |
37 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(34): 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 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0018 others(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 | a0001c0001t0003 a0001c0001t0012 a0001c0003t0006 others(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 | a0002c0002t0005 a0002c0012t0005 a0010c0021t0005 |
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 | a0001c0003t0002 a0001c0003t0006 a0001c0011t0002 others(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 | a0001c0003t0002 a0001c0003t0006 a0001c0011t0002 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10026687 | C | G | 1 | a0002c0002t0002g0237 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0003g0005 | 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 | a0007c0007t0003g0151 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0012g0149 | 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 | 31 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0125 others(28): 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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0003c0004t0003g0156 | 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 | a0001c0001t0001g0006 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | 7 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0003g0144 others(4): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0192 a0002c0002t0002g0194 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): 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 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0004g0118 others(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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0006g0193 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0119 |
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 | a0003c0004t0003g0156 | 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 | a0001c0001t0001g0025 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0006g0193 |
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 | 96 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(93): Show |
97 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(94): 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0001c0023t0001g0027 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0002c0002t0005g0173 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0028 | 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 | a0001c0003t0002g0003 a0001c0003t0006g0003 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0005g0228 | 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 | a0002c0002t0002g0196 | 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 | a0005c0008t0007g0023 a0005c0008t0007g0024 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0003g0125 others(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 | 140 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0038 others(137): Show |
141 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(138): 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 | 135 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(132): Show |
136 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(133): 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 | a0005c0008t0001g0022 | 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 | 160 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(157): Show |
161 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(158): 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0192 others(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 | a0001c0001t0008g0034 | 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 | a0001c0001t0008g0034 | 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 | a0003c0004t0003g0162 | 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 | a0002c0002t0005g0173 a0002c0002t0005g0215 |
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 | a0002c0002t0005g0173 a0002c0002t0005g0215 |
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 | a0002c0002t0005g0173 a0002c0002t0005g0215 |
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 | a0001c0016t0003g0122 a0004c0005t0001g0165 a0004c0005t0001g0166 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0119 a0001c0011t0002g0195 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0023t0001g0027 | 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 | a0002c0002t0002g0191 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0002c0002t0002g0196 | 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 | a0001c0001t0001g0006 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0006 a0001c0011t0002g0195 a0001c0011t0003g0235 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | 133 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(130): 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 | a0001c0001t0003g0069 | 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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0004g0066 | 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 | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): 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 | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0068 others(36): 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0206 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0180 a0002c0002t0002g0210 others(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 | a0002c0002t0005g0173 a0002c0002t0005g0177 a0002c0002t0005g0214 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0104 |
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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): 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 | a0001c0001t0001g0008 a0006c0006t0002g0219 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0008 a0001c0011t0002g0195 a0001c0011t0003g0235 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0013c0015t0001g0035 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0204 a0002c0002t0002g0230 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0004g0063 others(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 | a0002c0002t0002g0222 | 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 | a0006c0006t0002g0219 a0006c0006t0014g0218 |
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 | a0001c0001t0018g0010 | 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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0013c0015t0001g0035 | 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 | a0001c0001t0001g0006 | 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0006g0193 |
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 | a0001c0001t0004g0061 | 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 | a0002c0002t0002g0206 a0002c0002t0002g0207 |
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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0002c0002t0002g0184 a0002c0002t0002g0185 a0002c0002t0002g0186 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0187 a0002c0002t0002g0188 others(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 | a0002c0002t0002g0191 a0002c0002t0002g0196 a0002c0002t0002g0201 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0222 a0002c0002t0005g0173 others(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 | a0002c0002t0002g0208 a0002c0002t0002g0220 a0002c0002t0002g0224 others(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 | a0002c0002t0002g0180 a0002c0002t0002g0192 a0002c0002t0005g0177 |
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 | a0001c0011t0002g0195 a0002c0002t0002g0194 a0002c0002t0002g0237 others(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 | a0002c0002t0002g0225 a0002c0002t0002g0226 a0002c0012t0005g0190 |
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 | a0002c0002t0002g0229 a0002c0002t0005g0228 |
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 | a0002c0002t0002g0230 | 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 | a0002c0002t0002g0232 a0002c0002t0005g0227 |
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 | a0002c0002t0002g0231 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0003g0125 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0175 a0002c0002t0006g0200 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0004c0005t0001g0167 a0004c0005t0001g0168 a0004c0005t0001g0171 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0004g0057 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0101 | 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 | a0002c0002t0002g0175 a0002c0002t0002g0201 a0002c0002t0006g0200 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0002c0002t0002g0186 a0002c0002t0002g0188 a0002c0002t0002g0236 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0106 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0008 a0001c0001t0004g0121 a0002c0002t0002g0180 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0158 a0003c0004t0003g0159 others(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 | a0003c0004t0003g0157 a0003c0004t0003g0161 a0007c0007t0003g0152 others(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 | 43 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(40): 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 | a0001c0016t0003g0122 a0004c0005t0001g0165 a0004c0005t0001g0166 others(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 | a0011c0017t0004g0062 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0003g0144 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0100 | 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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0001c0001t0001g0011 a0001c0001t0004g0041 a0001c0001t0004g0056 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0076 a0001c0001t0001g0106 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0013c0015t0001g0035 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0077 |
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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0012c0014t0013g0150 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0068 | 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 | a0006c0006t0002g0217 | 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 | a0002c0002t0002g0205 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0206 a0002c0002t0002g0207 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0004g0042 a0001c0001t0004g0063 |
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 | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(15): 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 | a0001c0003t0002g0128 a0002c0002t0002g0236 a0003c0004t0003g0156 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | ||||||
| chr3:10041843 | T | TC | 2 | a0001c0001t0003g0143 a0001c0001t0003g0146 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.783+133_783+134ins others(1): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 10/43 | chr3 | 10041843 | |||||||
| chr3:10041854 | T | C | 1 | a0002c0002t0005g0214 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0013c0015t0001g0035 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | 36 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(33): 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 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0015c0018t0004g0079 | 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 | a0001c0001t0001g0099 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0009c0010t0003g0154 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0201 a0002c0002t0006g0200 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0007 a0005c0008t0001g0022 a0005c0008t0007g0023 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0072 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0109 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0004g0118 a0001c0001t0007g0113 a0001c0011t0002g0195 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0210 a0002c0002t0002g0225 a0002c0002t0005g0173 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0180 a0002c0002t0002g0183 others(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 | a0001c0001t0001g0025 a0001c0001t0004g0043 a0001c0016t0003g0122 others(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 | a0012c0014t0013g0150 | 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 | a0009c0010t0003g0155 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0159 others(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 | a0009c0010t0003g0154 | 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 | a0003c0004t0003g0158 a0003c0004t0003g0160 a0003c0004t0003g0163 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | 38 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(35): 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0006g0193 |
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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0206 others(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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0114 a0001c0001t0004g0121 a0001c0003t0002g0137 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0185 a0002c0002t0002g0224 others(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 | 37 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(34): 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0158 a0003c0004t0003g0159 others(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 | a0002c0002t0006g0198 a0003c0004t0003g0157 a0009c0010t0003g0154 |
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 | a0002c0002t0002g0202 a0002c0002t0002g0205 a0002c0002t0002g0210 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0187 a0002c0002t0002g0199 a0002c0002t0002g0201 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0201 a0002c0002t0006g0200 |
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 | a0001c0003t0002g0134 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | 54 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(51): 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 | a0002c0002t0002g0210 a0002c0002t0005g0173 a0002c0002t0005g0177 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0003g0136 a0001c0001t0003g0138 a0001c0001t0003g0139 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0012c0014t0013g0150 | 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0072 others(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 | a0001c0001t0003g0037 | 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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0006c0006t0002g0217 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | 134 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(131): 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0158 a0003c0004t0003g0159 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0002c0002t0002g0196 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0006c0006t0015g0216 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0002c0002t0002g0202 a0002c0002t0002g0205 |
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 | a0003c0004t0003g0164 | 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0179 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0181 others(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 | a0012c0014t0013g0150 | 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 | a0002c0002t0017g0174 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(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 | a0001c0001t0004g0074 a0001c0011t0002g0195 a0001c0011t0003g0235 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0179 others(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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0003c0004t0003g0159 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0001c0001t0001g0105 | 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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0003c0004t0003g0161 | 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 | a0001c0001t0001g0031 | 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 | 37 | a0001c0001t0001g0048 a0001c0001t0004g0002 a0001c0001t0004g0009 others(34): Show |
37 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(34): 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0105 a0004c0005t0001g0167 others(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 | a0006c0006t0002g0217 a0006c0006t0002g0219 a0006c0006t0014g0218 others(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 | 39 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0068 others(36): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0004g0009 | 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0159 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(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 | a0002c0002t0005g0177 a0002c0012t0005g0189 |
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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(99): Show |
102 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(99): 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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0181 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0016t0003g0122 a0002c0002t0002g0199 a0002c0002t0002g0201 others(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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): 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 | a0002c0002t0002g0206 | 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 | a0002c0002t0002g0206 a0002c0002t0002g0207 a0002c0002t0002g0208 others(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 | a0002c0002t0002g0206 a0002c0002t0002g0207 a0002c0002t0002g0208 others(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 | |||||||
| chr3:10051473 | G | T | 1 | a0012c0014t0013g0150 | 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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | 4 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0091 others(1): 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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0002c0002t0002g0206 a0002c0002t0002g0207 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0158 a0003c0004t0003g0159 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0114 a0001c0011t0002g0195 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0179 others(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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0012c0014t0013g0150 | 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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0009c0010t0003g0154 | 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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0028 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0009c0010t0003g0155 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0008g0033 a0001c0001t0008g0034 a0001c0001t0008g0053 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0009c0010t0003g0155 | 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 | a0012c0014t0013g0150 | 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 | a0012c0014t0013g0150 | 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 | 11 | a0001c0001t0003g0004 a0001c0001t0003g0136 a0001c0001t0003g0138 others(8): 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0072 | 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0013 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0009c0010t0003g0155 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0003g0141 | 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0004g0110 a0001c0016t0003g0122 a0004c0005t0001g0165 others(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 | a0001c0001t0010g0030 a0001c0003t0002g0123 a0001c0003t0002g0128 |
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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0232 |
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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0090 others(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 | a0001c0001t0004g0066 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0085 others(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 | 35 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(32): 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 | a0002c0002t0006g0197 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0037 others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0003g0145 | 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 | CGT | 2 | a0001c0001t0003g0141 a0001c0001t0003g0145 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1656+1914_1656+191 others(6): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr3 | 10054410 | ||||||
| chr3:10054410 | C | T | 1 | a0001c0001t0008g0033 | 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 | a0001c0001t0003g0004 a0001c0001t0012g0149 |
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 | a0001c0001t0003g0005 a0001c0001t0003g0037 a0001c0001t0003g0136 others(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 | a0001c0001t0003g0148 | 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 | a0001c0001t0003g0037 a0001c0001t0003g0136 a0001c0001t0003g0138 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0181 others(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 | a0001c0001t0003g0004 a0001c0001t0012g0149 |
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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0001c0001t0001g0077 a0003c0004t0003g0157 a0003c0004t0003g0159 others(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 | a0003c0004t0003g0158 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0162 a0003c0004t0003g0163 others(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 | a0009c0010t0003g0154 | 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 | a0002c0002t0002g0206 a0002c0002t0006g0193 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0032 others(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 | 30 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(27): 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 | |||||||
| chr3:10054443 | A | ACATG | 2 | a0002c0002t0002g0206 a0002c0002t0006g0193 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1656+1946_1656+194 others(8): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054443 | |||||||
| chr3:10054444 | T | C | 1 | a0002c0002t0002g0204 | 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 | a0004c0005t0016g0170 | 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 | 38 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(35): 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 | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(39): 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 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(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 | a0002c0002t0002g0204 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0002c0002t0002g0206 a0002c0002t0006g0193 |
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 | a0003c0004t0003g0157 a0003c0004t0003g0159 a0003c0004t0003g0160 others(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 | a0003c0004t0003g0158 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0002c0002t0002g0204 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0162 a0003c0004t0003g0163 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0012c0014t0013g0150 | 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 | a0009c0010t0003g0154 | 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 | a0001c0001t0001g0107 a0002c0002t0002g0226 a0002c0002t0005g0213 others(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 | a0002c0002t0002g0210 | 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 | a0001c0001t0001g0012 a0001c0001t0004g0057 a0001c0001t0004g0066 others(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 | a0001c0001t0003g0132 a0002c0002t0002g0191 a0002c0002t0002g0192 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0003g0125 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0003g0133 others(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 | a0013c0015t0001g0035 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0080 a0001c0001t0003g0037 others(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 | a0001c0001t0003g0140 a0001c0001t0003g0143 a0001c0001t0003g0147 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0120 others(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 | a0001c0001t0003g0145 | 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 | a0001c0001t0004g0047 a0001c0001t0008g0034 a0004c0005t0001g0165 others(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 | a0001c0001t0011g0054 a0002c0002t0002g0180 a0002c0002t0002g0207 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0194 a0002c0002t0002g0225 others(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 | a0002c0002t0002g0202 a0002c0002t0005g0209 a0002c0002t0005g0227 others(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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): 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 | a0003c0004t0003g0157 a0003c0004t0003g0158 a0003c0004t0003g0160 others(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 | ||||||
| chr3:10054474 | T | TATA | 2 | a0001c0001t0004g0052 a0001c0001t0004g0063 |
2 | HG01255.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1656+1977_1656+197 others(7): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 18/43 | chr3 | 10054474 | |||||||
| chr3:10054475 | T | A | 7 | a0001c0001t0001g0076 a0001c0001t0004g0051 a0003c0004t0003g0156 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0013c0015t0001g0035 | 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 | a0002c0002t0002g0179 a0002c0002t0002g0220 a0002c0002t0002g0221 others(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 | a0001c0001t0003g0125 a0001c0011t0002g0195 a0001c0011t0003g0235 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0012g0149 | 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 | a0005c0008t0001g0022 | 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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0012c0014t0013g0150 | 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 | a0002c0002t0002g0180 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0106 |
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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0001c0016t0003g0122 others(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 | a0015c0018t0004g0079 | 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 | a0001c0001t0012g0149 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0002c0002t0002g0202 a0002c0002t0002g0205 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0003g0037 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0012g0149 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0004g0060 | 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 | 4 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0064 others(1): Show |
4 | HG01243.hp1 HG01255.hp2 HG03017.hp1 others(1): 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0105 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | 3 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0003g0146 |
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 | a0002c0002t0002g0224 | 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0001g0031 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0001c0001t0008g0033 a0001c0001t0008g0034 a0001c0001t0008g0053 others(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 | a0001c0001t0004g0009 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0106 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0005g0214 others(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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0001g0120 a0001c0001t0004g0045 a0001c0011t0002g0195 others(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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0002c0002t0002g0199 | 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 | a0001c0011t0002g0195 a0001c0011t0003g0235 a0002c0002t0002g0175 others(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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0001c0011t0003g0235 a0002c0002t0002g0181 a0002c0002t0002g0182 others(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 | a0012c0014t0013g0150 | 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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0206 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0206 others(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 | a0013c0015t0001g0035 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0018 | 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 | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(36): 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 | a0012c0014t0013g0150 | 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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0108 | 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 | a0001c0011t0003g0235 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0101 |
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 | a0001c0001t0004g0049 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0001c0001t0001g0025 | 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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0009c0010t0003g0154 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0004c0005t0001g0166 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(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 | a0002c0002t0002g0224 | 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 | a0001c0001t0003g0037 | 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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0002c0002t0002g0186 a0002c0002t0002g0188 |
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 | a0001c0001t0001g0093 | 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 | a0009c0010t0003g0154 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0012g0149 | 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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0002c0002t0002g0180 a0002c0002t0002g0225 a0002c0002t0006g0197 |
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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | 7 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0076 others(4): 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 | a0001c0001t0001g0109 | 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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0002c0002t0002g0180 a0002c0002t0002g0225 a0002c0002t0006g0197 |
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 | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(36): 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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0002c0002t0002g0175 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0206 a0002c0002t0002g0207 |
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 | a0012c0014t0013g0150 | 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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0012g0149 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0003c0004t0003g0163 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | 44 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0068 others(41): 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 | ||||||
| chr3:10069462 | TCTCCCC | T | 2 | a0001c0001t0001g0006 a0001c0001t0004g0043 |
2 | HG01243.hp2 HG03486.hp2 |
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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0016t0003g0122 a0012c0014t0013g0150 |
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 | a0012c0014t0013g0150 | 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 | a0001c0001t0001g0085 | 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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0159 | 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 | a0007c0007t0003g0151 | 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 | a0007c0007t0003g0153 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0162 a0009c0010t0003g0154 |
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 | a0009c0010t0003g0155 | 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 | a0007c0007t0003g0152 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0092 | 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 | a0002c0002t0002g0181 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0105 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0007c0007t0003g0153 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0004g0052 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
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 | a0002c0002t0002g0192 | 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 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
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 | a0001c0001t0004g0074 a0001c0003t0002g0123 a0002c0002t0017g0174 others(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 | a0001c0001t0001g0097 | 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 | a0002c0002t0005g0213 a0002c0002t0009g0212 |
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 | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(36): 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0107 a0001c0016t0003g0122 a0003c0004t0003g0156 others(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 | a0002c0002t0002g0208 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0099 | 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(207): Show |
1 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0104 a0001c0001t0003g0141 a0005c0008t0001g0022 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0105 a0001c0001t0003g0146 others(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 |
143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0004g0044 a0001c0001t0004g0056 a0001c0001t0004g0121 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0004g0044 a0001c0001t0004g0056 a0001c0001t0004g0121 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0001t0004g0044 a0001c0001t0004g0056 a0001c0001t0004g0121 |
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 | a0002c0002t0002g0203 a0002c0002t0002g0204 |
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 | a0002c0002t0017g0174 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0163 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0003g0125 a0001c0001t0003g0127 a0001c0001t0003g0132 others(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 | |||||||
| chr3:10070762 | C | G | 4 | a0006c0006t0002g0217 a0006c0006t0002g0219 a0006c0006t0014g0218 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0032 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0015c0018t0004g0079 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0012c0014t0013g0150 | 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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0032 others(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 | a0001c0001t0001g0017 | 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0002c0002t0017g0174 | 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 | a0001c0001t0008g0033 a0001c0001t0008g0034 a0001c0001t0008g0053 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0006 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0075 a0015c0018t0004g0079 |
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 | a0002c0002t0002g0180 a0002c0002t0002g0225 a0002c0002t0006g0197 |
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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0002g0210 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0001t0001g0086 a0001c0001t0003g0125 a0001c0001t0003g0127 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0206 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0067 a0001c0001t0007g0036 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0006c0006t0002g0217 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0064 |
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 | a0002c0002t0002g0199 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0006c0006t0002g0217 | 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 | a0001c0001t0004g0009 | 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 | a0011c0017t0004g0062 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0002g0191 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | CA | 2 | a0001c0001t0003g0125 a0001c0011t0003g0235 |
2 | HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2859+515_2859+516i others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10075188 | |||||||
| chr3:10075188 | C | CT | 66 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0002g0234 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0004g0057 | 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 | a0012c0014t0013g0150 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | 3 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0003g0146 |
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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): 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 | 44 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(41): 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0210 a0002c0002t0005g0173 a0002c0002t0005g0177 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0080 a0001c0011t0002g0195 others(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 | a0001c0001t0001g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2859+1419A>G | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 29/43 | chr3 | 10076092 | |||||||
| chr3:10076153 | T | TATGCTTC others(7): Show |
4 | a0002c0002t0002g0184 a0002c0002t0002g0186 a0002c0002t0002g0188 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0004g0065 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0004g0043 | 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 | a0002c0002t0002g0232 | 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 | a0006c0006t0015g0216 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0006 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0019g0050 | 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 | a0001c0001t0001g0071 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(36): 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0005g0211 | 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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0006g0193 |
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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0088 | 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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0005g0215 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0006c0006t0002g0219 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0012g0149 | 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 | a0002c0002t0002g0210 a0002c0002t0005g0173 a0002c0002t0005g0177 others(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 | a0001c0001t0001g0097 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0012c0014t0013g0150 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0085 |
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 | a0013c0015t0001g0035 | 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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0001c0001t0001g0031 | 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 | 133 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(130): 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 | a0001c0001t0001g0109 | 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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0002c0002t0002g0185 | 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 | a0002c0002t0002g0175 a0002c0002t0002g0199 a0002c0002t0002g0202 others(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 | a0001c0016t0003g0122 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0004g0009 a0011c0017t0004g0062 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0077 |
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 | a0002c0002t0002g0186 a0002c0002t0002g0188 |
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 | a0001c0001t0001g0011 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0011t0002g0195 | 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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0003c0004t0003g0163 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0004g0041 a0001c0001t0004g0066 a0001c0001t0004g0118 |
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 | a0001c0001t0004g0063 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0009c0010t0003g0154 a0009c0010t0003g0155 |
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 | a0012c0014t0013g0150 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0011t0002g0195 a0001c0016t0003g0122 a0002c0002t0002g0175 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0038 | 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 | a0012c0014t0013g0150 | 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 | a0002c0002t0005g0227 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0002c0002t0002g0179 a0002c0020t0002g0223 |
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 | a0001c0001t0001g0008 a0001c0016t0003g0122 a0003c0004t0003g0156 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0007c0007t0003g0151 a0007c0007t0003g0152 a0007c0007t0003g0153 |
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 | a0002c0002t0002g0175 a0002c0002t0002g0201 a0002c0002t0006g0200 |
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 | a0002c0002t0005g0213 a0002c0002t0009g0212 |
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 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
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 | a0009c0010t0003g0155 | 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 | a0002c0002t0002g0210 a0002c0002t0005g0173 a0002c0002t0005g0177 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0007c0007t0003g0151 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0059 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0012t0005g0189 a0002c0012t0005g0190 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0101 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0003t0002g0123 a0001c0003t0002g0128 a0001c0003t0002g0131 |
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 | a0009c0010t0003g0155 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0179 a0002c0002t0002g0180 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0002c0002t0002g0181 a0002c0002t0002g0182 a0002c0002t0002g0229 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0226 a0002c0002t0005g0173 others(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 | a0001c0001t0004g0060 | 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 | a0002c0002t0002g0206 a0002c0002t0002g0207 a0002c0002t0002g0208 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0210 a0002c0002t0005g0173 a0002c0002t0005g0177 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0003g0069 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0028 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
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 | a0002c0002t0006g0198 | 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0004g0056 | 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 | a0002c0002t0002g0199 | 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 | a0002c0002t0005g0228 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0087 |
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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0081 a0001c0001t0012g0149 a0004c0005t0001g0165 others(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 | a0003c0004t0003g0157 a0003c0004t0003g0159 a0003c0004t0003g0160 others(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 | a0002c0002t0002g0187 a0002c0002t0002g0192 a0002c0002t0002g0206 others(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 | a0001c0003t0002g0123 a0001c0003t0002g0124 a0001c0003t0002g0135 others(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 | a0001c0001t0003g0037 a0001c0003t0002g0003 a0001c0003t0002g0126 others(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 | a0006c0006t0014g0218 | 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 | a0002c0002t0002g0225 | 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 | a0012c0014t0013g0150 | 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 | a0001c0001t0007g0113 a0003c0004t0003g0162 |
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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0005c0008t0007g0023 a0005c0008t0007g0024 a0014c0022t0007g0021 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0196 others(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 | a0001c0001t0004g0059 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0089 others(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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0001c0001t0004g0049 | 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 | a0005c0008t0001g0022 a0005c0008t0007g0023 a0005c0008t0007g0024 others(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 | a0001c0001t0003g0103 | 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 | a0001c0001t0001g0086 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0001t0003g0140 | 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 | a0001c0001t0001g0094 a0004c0005t0001g0165 a0004c0005t0001g0166 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0003c0004t0003g0158 a0003c0004t0003g0159 |
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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | 40 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(37): 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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0005c0013t0001g0115 a0005c0013t0001g0116 |
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 | a0001c0001t0004g0043 | 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 | 27 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(24): 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 | a0001c0001t0001g0007 a0001c0001t0001g0072 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0055 others(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 | 108 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0067 others(105): 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 | a0001c0016t0003g0122 a0002c0002t0002g0229 a0002c0002t0002g0230 others(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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0002c0002t0002g0229 a0002c0002t0002g0230 a0002c0002t0002g0231 others(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 | a0012c0014t0013g0150 | 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 | a0001c0001t0001g0096 | 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 | a0007c0007t0003g0152 | 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 | a0002c0002t0002g0226 a0002c0002t0005g0227 a0002c0002t0005g0228 others(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 | a0006c0006t0014g0218 | 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 | a0001c0011t0003g0235 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0010c0021t0005g0178 | 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 | a0001c0001t0004g0057 a0001c0001t0004g0060 |
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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0002c0002t0002g0181 a0002c0002t0002g0182 a0002c0002t0002g0183 others(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 | a0002c0002t0002g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3963+141T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094504 | |||||||
| chr3:10094641 | C | T | 11 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0007c0007t0003g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3963+342T>A | FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094705 | |||||||
| chr3:10094705 | T | TA | 2 | a0002c0002t0002g0226 a0002c0002t0002g0237 |
2 | HG01928.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3963+342_3963+343i others(3): Show |
FANCD2 | ENSG00000144554.13 | transcript | ENST00000675286.1 | protein_coding | 40/43 | chr3 | 10094705 | |||||||
| chr3:10094706 | T | A | 106 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0001t0003g0069 | 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 | a0002c0002t0002g0196 | 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 | a0001c0001t0004g0065 | 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 | a0012c0014t0013g0150 | 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 | a0012c0014t0013g0150 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0104 a0001c0001t0003g0103 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0124 a0001c0003t0002g0126 others(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 | a0001c0003t0002g0123 a0001c0003t0002g0130 a0002c0002t0002g0181 others(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 | 9 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0090 others(6): 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 | a0012c0014t0013g0150 | 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 | a0012c0014t0013g0150 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0012c0014t0013g0150 | 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 | a0002c0002t0002g0206 a0002c0002t0002g0207 |
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 | a0012c0014t0013g0150 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0002c0002t0002g0180 | 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 | a0013c0015t0001g0035 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0009c0010t0003g0154 a0009c0010t0003g0155 |
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 | a0001c0001t0001g0092 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0006c0006t0002g0219 a0006c0006t0014g0218 a0006c0006t0015g0216 |
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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0009c0010t0003g0155 | 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 | a0002c0002t0002g0199 | 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 | a0012c0014t0013g0150 | 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 | a0003c0004t0003g0156 a0003c0004t0003g0157 a0003c0004t0003g0158 others(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 | a0012c0014t0013g0150 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0012c0014t0013g0150 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0013c0015t0001g0035 | 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 | a0013c0015t0001g0035 | 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 | 128 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0037 others(125): 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | a0001c0011t0003g0235 a0003c0004t0003g0156 a0003c0004t0003g0157 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 | 19 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0037 others(16): 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 | 37 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0041 others(34): Show |
37 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(34): 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 | a0004c0005t0001g0165 a0004c0005t0001g0166 a0004c0005t0001g0167 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0101 |
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 | a0002c0002t0017g0174 | 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 | a0001c0011t0002g0195 a0002c0002t0002g0175 a0002c0002t0002g0179 others(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 | a0002c0002t0002g0225 | 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 | 169 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0108 others(166): Show |
170 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(167): 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 | a0009c0010t0003g0155 | 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 | a0002c0002t0005g0227 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0123 a0001c0003t0002g0124 others(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 |