| geneid | 2324 |
|---|---|
| ensemblid | ENSG00000037280.16 |
| hgncid | 3767 |
| symbol | FLT4 |
| name | fms related receptor tyrosine kinase 4 |
| refseq_nuc | NM_182925.5 |
| refseq_prot | NP_891555.2 |
| ensembl_nuc | ENST00000261937.11 |
| ensembl_prot | ENSP00000261937.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180601506 |
| end | 180649600 |
| strand | - |
| ver | v1.2 |
| region | chr5:180601506-180649600 |
| region5000 | chr5:180596506-180654600 |
| regionname0 | FLT4_chr5_180601506_180649600 |
| regionname5000 | FLT4_chr5_180596506_180654600 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1363 | 176 | 38 | 42 | 76 | 4 | 16 | 53 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002 | 0/0 | 1363 | 153 | 34 | 20 | 71 | 8 | 20 | 46 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0003 | 0/0 | 1363 | 9 | 1 | 7 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0004 | 0/0 | 1363 | 6 | 0 | 4 | 0 | 1 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005 | 0/0 | 1363 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006 | 0/0 | 1363 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0007 | 0/0 | 1363 | 4 | 2 | 1 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0008 | 0/0 | 1363 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0009 | 0/0 | 1363 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0010 | 0/0 | 1363 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0011 | 0/0 | 1363 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0012 | 0/0 | 1363 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0013 | 0/0 | 1363 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0014 | 0/0 | 1363 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0015 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0016 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0017 | 0/0 | 1363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0018 | 0/0 | 1363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0019 | 0/0 | 1363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0020 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0021 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0022 | 0/0 | 1363 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0023 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0024 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0025 | 0/0 | 1363 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0026 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0027 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0028 | 0/0 | 1363 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0029 | 0/0 | 1363 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0030 | 0/0 | 1363 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0031 | 0/0 | 1363 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4092 | 155 | 33 | 36 | 66 | 4 | 16 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0002 | 0/0 | 4092 | 67 | 4 | 18 | 30 | 4 | 11 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0003 | 0/0 | 4092 | 51 | 26 | 1 | 17 | 2 | 5 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0004 | 0/0 | 4092 | 17 | 1 | 1 | 13 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0005 | 0/0 | 4092 | 9 | 1 | 7 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0006 | 0/0 | 4092 | 6 | 0 | 4 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0007 | 0/0 | 4092 | 6 | 0 | 4 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0008 | 0/0 | 4092 | 5 | 0 | 0 | 5 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0009 | 0/0 | 4092 | 5 | 0 | 2 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0010 | 0/0 | 4092 | 4 | 2 | 1 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0011 | 0/0 | 4092 | 4 | 0 | 0 | 1 | 0 | 3 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0012 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0013 | 0/0 | 4092 | 3 | 0 | 0 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0014 | 0/0 | 4092 | 3 | 2 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0015 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0016 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0017 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0018 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0019 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0020 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0021 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0022 | 0/0 | 4092 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0023 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0024 | 0/0 | 4092 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0025 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0026 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0027 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0028 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0029 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0030 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0031 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0032 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0033 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0034 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0035 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0036 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0037 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0038 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0039 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0040 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0041 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0042 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0043 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0044 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0045 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0046 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0047 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0048 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0049 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0050 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0051 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0052 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| c0053 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1742 | 163 | 19 | 53 | 55 | 14 | 22 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0002 | 0/0 | 1742 | 59 | 23 | 12 | 22 | 0 | 2 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0003 | 0/0 | 1742 | 32 | 3 | 1 | 27 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0004 | 0/0 | 1742 | 30 | 2 | 1 | 22 | 0 | 5 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0005 | 0/0 | 1742 | 22 | 1 | 2 | 14 | 2 | 3 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0006 | 0/0 | 1742 | 13 | 1 | 4 | 1 | 0 | 7 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0007 | 0/0 | 1742 | 11 | 11 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0008 | 0/0 | 1742 | 5 | 4 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0009 | 0/0 | 1742 | 5 | 5 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0010 | 0/0 | 1742 | 5 | 4 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0011 | 0/0 | 1742 | 5 | 5 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0012 | 0/0 | 1742 | 5 | 2 | 1 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0013 | 0/0 | 1742 | 4 | 4 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0014 | 0/0 | 1742 | 3 | 0 | 1 | 1 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0015 | 0/0 | 1742 | 3 | 2 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0016 | 0/0 | 1742 | 3 | 0 | 0 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0017 | 0/0 | 1742 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0018 | 0/0 | 1742 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0019 | 0/0 | 1742 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0020 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0021 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0022 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0023 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0024 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0025 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0026 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0027 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0028 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0029 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0030 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0031 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0032 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| t0033 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4092 | 155 | 33 | 36 | 66 | 4 | 16 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0006 | 0/0 | 4092 | 6 | 0 | 4 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0009 | 0/0 | 4092 | 5 | 0 | 2 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0013 | 0/0 | 4092 | 3 | 0 | 0 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0023 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0031 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0032 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0043 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0047 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0052 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002 | 0/0 | 4092 | 67 | 4 | 18 | 30 | 4 | 11 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003 | 0/0 | 4092 | 51 | 26 | 1 | 17 | 2 | 5 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0004 | 0/0 | 4092 | 17 | 1 | 1 | 13 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0008 | 0/0 | 4092 | 5 | 0 | 0 | 5 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0011 | 0/0 | 4092 | 4 | 0 | 0 | 1 | 0 | 3 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0012 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0022 | 0/0 | 4092 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0029 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0035 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0038 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0041 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0003c0005 | 0/0 | 4092 | 9 | 1 | 7 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0004c0007 | 0/0 | 4092 | 6 | 0 | 4 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005c0015 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005c0018 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006c0014 | 0/0 | 4092 | 3 | 2 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006c0033 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0007c0010 | 0/0 | 4092 | 4 | 2 | 1 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0008c0025 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0008c0027 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0009c0024 | 0/0 | 4092 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0010c0021 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0011c0016 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0012c0017 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0013c0019 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0014c0020 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0015c0026 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0016c0051 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0017c0049 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0018c0039 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0019c0040 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0020c0044 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0021c0034 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0022c0045 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0023c0036 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0024c0046 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0025c0037 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0026c0030 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0027c0042 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0028c0048 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0029c0028 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0030c0050 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0031c0053 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5833 | 73 | 11 | 17 | 33 | 2 | 10 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0002 | 0/0 | 5833 | 46 | 16 | 10 | 19 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0003 | 0/0 | 5833 | 3 | 0 | 0 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0004 | 0/0 | 5833 | 5 | 0 | 0 | 5 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0005 | 0/0 | 5833 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0006 | 0/0 | 5833 | 11 | 1 | 4 | 1 | 0 | 5 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0008 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0010 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0012 | 0/0 | 5833 | 5 | 2 | 1 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0015 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0016 | 0/0 | 5833 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0020 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0024 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0025 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0027 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0001t0029 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0006t0001 | 0/0 | 5833 | 5 | 0 | 4 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0006t0002 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0009t0001 | 0/0 | 5833 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0009t0002 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0009t0004 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0009t0014 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0013t0001 | 0/0 | 5833 | 3 | 0 | 0 | 3 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0023t0008 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0031t0016 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0032t0026 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0043t0002 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0047t0001 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0001c0052t0001 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0001 | 0/0 | 5833 | 40 | 0 | 16 | 14 | 4 | 6 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0003 | 0/0 | 5833 | 5 | 1 | 0 | 4 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0004 | 0/0 | 5833 | 16 | 2 | 1 | 10 | 0 | 3 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0005 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0013 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0014 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0018 | 0/0 | 5833 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0002t0022 | 0/0 | 5855 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0001 | 0/0 | 5833 | 8 | 5 | 0 | 0 | 2 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0002 | 0/0 | 5833 | 5 | 5 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0003 | 0/0 | 5833 | 20 | 2 | 1 | 16 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0005 | 0/0 | 5833 | 2 | 0 | 0 | 1 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0006 | 0/0 | 5833 | 2 | 0 | 0 | 0 | 0 | 2 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0007 | 0/0 | 5833 | 9 | 9 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0010 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0013 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0003t0019 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0004t0003 | 0/0 | 5833 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0004t0005 | 0/0 | 5833 | 13 | 1 | 1 | 9 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0004t0031 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0004t0033 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0008t0004 | 0/0 | 5833 | 4 | 0 | 0 | 4 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0008t0032 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0011t0004 | 0/0 | 5833 | 3 | 0 | 0 | 1 | 0 | 2 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0011t0014 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0012t0001 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0012t0021 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0012t0023 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0022t0003 | 0/0 | 5833 | 2 | 0 | 0 | 2 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0029t0001 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0035t0001 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0038t0004 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0002c0041t0005 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0003c0005t0001 | 0/0 | 5833 | 8 | 1 | 6 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0003c0005t0002 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0004c0007t0001 | 0/0 | 5833 | 6 | 0 | 4 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005c0015t0011 | 0/0 | 5833 | 3 | 3 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005c0018t0011 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0005c0018t0013 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006c0014t0002 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006c0014t0009 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0006c0033t0009 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0007c0010t0001 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0007c0010t0010 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0007c0010t0015 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0008c0025t0017 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0008c0027t0017 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0009c0024t0001 | 0/0 | 5833 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0010c0021t0001 | 0/0 | 5833 | 2 | 0 | 0 | 0 | 1 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0011c0016t0007 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0011c0016t0011 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0012c0017t0001 | 0/0 | 5833 | 2 | 0 | 0 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0013c0019t0008 | 0/0 | 5833 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0014c0020t0007 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0014c0020t0013 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0015c0026t0002 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0016c0051t0002 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0017c0049t0005 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0018c0039t0001 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0019c0040t0002 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0020c0044t0005 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0021c0034t0009 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0022c0045t0005 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0023c0036t0001 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0024c0046t0009 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0025c0037t0001 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0026c0030t0030 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0027c0042t0028 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0028c0048t0001 | 0/0 | 5833 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0029c0028t0010 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0030c0050t0001 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| a0031c0053t0001 | 0/0 | 5833 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | copy fasta | chr5 | 180596506 | 180654600 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0006g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0010g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0012g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0012g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0012g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0012g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0015g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0020g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0024g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0027g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0001t0029g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0006t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0009t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0009t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0009t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0009t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0009t0014g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0013t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0013t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0023t0008g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0023t0008g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0031t0016g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0032t0026g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0043t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0047t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0001c0052t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0005g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0014g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0018g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0018g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0002t0022g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0006g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0006g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0007g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0003t0019g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0031g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0004t0033g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0008t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0008t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0008t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0008t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0008t0032g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0011t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0011t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0011t0014g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0012t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0012t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0012t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0022t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0022t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0029t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0035t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0038t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0002c0041t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0003c0005t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0004c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0005c0015t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0005c0015t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0005c0015t0011g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0005c0018t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0005c0018t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0006c0014t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0006c0014t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0006c0014t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0006c0033t0009g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0007c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0007c0010t0010g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0007c0010t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0007c0010t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0008c0025t0017g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0008c0027t0017g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0009c0024t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0010c0021t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0010c0021t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0011c0016t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0011c0016t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0012c0017t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0012c0017t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0013c0019t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0013c0019t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0014c0020t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0014c0020t0013g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0015c0026t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0016c0051t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0017c0049t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0018c0039t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0019c0040t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0020c0044t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0021c0034t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0022c0045t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0023c0036t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0024c0046t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0025c0037t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0026c0030t0030g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0027c0042t0028g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0028c0048t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0029c0028t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0030c0050t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| a0031c0053t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00099 | hp2 | a0002 | c0004 | t0005 | g0053 | EUR | GBR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00140 | hp2 | a0031 | c0053 | t0001 | g0380 | EUR | GBR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | FIN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00280 | hp2 | a0001 | c0001 | t0012 | g0357 | EUR | FIN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00323 | hp1 | a0007 | c0010 | t0001 | g0245 | EUR | FIN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0358 | EUR | FIN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00438 | hp2 | a0002 | c0004 | t0005 | g0278 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0099 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00544 | hp2 | a0002 | c0004 | t0005 | g0145 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00597 | hp1 | a0002 | c0003 | t0003 | g0362 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00597 | hp2 | a0001 | c0001 | t0016 | g0023 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00609 | hp1 | a0002 | c0029 | t0001 | g0228 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00621 | hp1 | a0002 | c0004 | t0005 | g0283 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00621 | hp2 | a0002 | c0004 | t0005 | g0026 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0345 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0005 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00642 | hp1 | a0003 | c0005 | t0002 | g0042 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0347 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00673 | hp1 | a0001 | c0013 | t0001 | g0151 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0108 | EAS | CHS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00733 | hp1 | a0009 | c0024 | t0001 | g0004 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0342 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00735 | hp1 | a0001 | c0001 | t0015 | g0332 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00735 | hp2 | a0004 | c0007 | t0001 | g0017 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00738 | hp1 | a0002 | c0004 | t0005 | g0322 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00741 | hp1 | a0001 | c0006 | t0001 | g0359 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01069 | hp2 | a0003 | c0005 | t0001 | g0036 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01070 | hp1 | a0002 | c0002 | t0014 | g0031 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0351 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0352 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0341 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01106 | hp1 | a0003 | c0005 | t0001 | g0037 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01106 | hp2 | a0009 | c0024 | t0001 | g0004 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0157 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01167 | hp1 | a0006 | c0014 | t0002 | g0374 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01168 | hp1 | a0025 | c0037 | t0001 | g0249 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01175 | hp1 | a0004 | c0007 | t0001 | g0185 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0292 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0234 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01243 | hp2 | a0007 | c0010 | t0010 | g0323 | AMR | PUR | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0337 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01256 | hp2 | a0003 | c0005 | t0001 | g0175 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0353 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01258 | hp2 | a0003 | c0005 | t0001 | g0176 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01346 | hp1 | a0001 | c0006 | t0001 | g0154 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01346 | hp2 | a0001 | c0009 | t0001 | g0019 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01358 | hp1 | a0022 | c0045 | t0005 | g0159 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01433 | hp1 | a0001 | c0009 | t0001 | g0063 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01433 | hp2 | a0003 | c0005 | t0001 | g0058 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01496 | hp2 | a0004 | c0007 | t0001 | g0015 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0348 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01516 | hp1 | a0010 | c0021 | t0001 | g0326 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01516 | hp2 | a0012 | c0017 | t0001 | g0329 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01517 | hp1 | a0012 | c0017 | t0001 | g0328 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01891 | hp1 | a0002 | c0004 | t0005 | g0364 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01891 | hp2 | a0002 | c0003 | t0003 | g0298 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01928 | hp2 | a0028 | c0048 | t0001 | g0219 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01934 | hp2 | a0001 | c0006 | t0001 | g0158 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01975 | hp1 | a0002 | c0003 | t0003 | g0192 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01975 | hp2 | a0001 | c0001 | t0029 | g0260 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01978 | hp2 | a0004 | c0007 | t0001 | g0010 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0101 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02040 | hp1 | a0002 | c0003 | t0003 | g0190 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0088 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02055 | hp2 | a0001 | c0043 | t0002 | g0230 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02056 | hp2 | a0002 | c0004 | t0005 | g0284 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0077 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02129 | hp2 | a0002 | c0003 | t0003 | g0274 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02132 | hp1 | a0002 | c0011 | t0004 | g0214 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02132 | hp2 | a0001 | c0001 | t0016 | g0262 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02135 | hp1 | a0002 | c0004 | t0005 | g0285 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | KHV | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02145 | hp2 | a0013 | c0019 | t0008 | g0059 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02148 | hp1 | a0001 | c0001 | t0025 | g0265 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0143 | EAS | CDX | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02155 | hp2 | a0001 | c0031 | t0016 | g0021 | EAS | CDX | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02165 | hp1 | a0002 | c0041 | t0005 | g0140 | EAS | CDX | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02257 | hp2 | a0005 | c0018 | t0013 | g0167 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0286 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02258 | hp2 | a0011 | c0016 | t0011 | g0181 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02280 | hp1 | a0011 | c0016 | t0007 | g0241 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02280 | hp2 | a0002 | c0003 | t0007 | g0006 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0363 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0331 | AMR | PEL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02451 | hp1 | a0007 | c0010 | t0015 | g0044 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02451 | hp2 | a0008 | c0025 | t0017 | g0009 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02572 | hp1 | a0005 | c0015 | t0011 | g0172 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02572 | hp2 | a0014 | c0020 | t0007 | g0170 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02602 | hp2 | a0019 | c0040 | t0002 | g0046 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02630 | hp2 | a0001 | c0001 | t0027 | g0231 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02647 | hp1 | a0002 | c0003 | t0010 | g0178 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0370 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0349 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02683 | hp2 | a0017 | c0049 | t0005 | g0213 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02698 | hp2 | a0003 | c0005 | t0001 | g0160 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0207 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02717 | hp2 | a0002 | c0003 | t0007 | g0314 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02723 | hp2 | a0002 | c0012 | t0023 | g0045 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02735 | hp1 | a0002 | c0011 | t0014 | g0166 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0032 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02738 | hp1 | a0004 | c0007 | t0001 | g0210 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0056 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02809 | hp1 | a0001 | c0047 | t0001 | g0173 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02809 | hp2 | a0006 | c0033 | t0009 | g0376 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02818 | hp2 | a0002 | c0003 | t0007 | g0242 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0052 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02895 | hp1 | a0002 | c0003 | t0019 | g0250 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02895 | hp2 | a0001 | c0023 | t0008 | g0378 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0325 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02896 | hp2 | a0002 | c0003 | t0010 | g0043 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0336 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02897 | hp2 | a0001 | c0023 | t0008 | g0377 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02965 | hp1 | a0001 | c0032 | t0026 | g0333 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0371 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02970 | hp2 | a0002 | c0003 | t0007 | g0373 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0343 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0291 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03041 | hp2 | a0002 | c0003 | t0007 | g0369 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0368 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03130 | hp1 | a0014 | c0020 | t0013 | g0271 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03139 | hp1 | a0002 | c0012 | t0021 | g0174 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03139 | hp2 | a0006 | c0014 | t0009 | g0301 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0375 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03195 | hp2 | a0027 | c0042 | t0028 | g0379 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03209 | hp1 | a0013 | c0019 | t0008 | g0060 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03225 | hp2 | a0007 | c0010 | t0015 | g0252 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03453 | hp1 | a0002 | c0003 | t0007 | g0006 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03453 | hp2 | a0024 | c0046 | t0009 | g0327 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03486 | hp1 | a0005 | c0018 | t0011 | g0041 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0317 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0344 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03516 | hp1 | a0015 | c0026 | t0002 | g0308 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03516 | hp2 | a0002 | c0003 | t0007 | g0238 | AFR | ESN | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03540 | hp2 | a0002 | c0003 | t0013 | g0240 | AFR | GWD | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03654 | hp1 | a0002 | c0035 | t0001 | g0221 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0122 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03688 | hp1 | a0002 | c0011 | t0004 | g0007 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03704 | hp1 | a0002 | c0003 | t0005 | g0318 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03704 | hp2 | a0002 | c0002 | t0022 | g0313 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03927 | hp1 | a0002 | c0003 | t0006 | g0334 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0266 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03942 | hp2 | a0002 | c0002 | t0005 | g0340 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04115 | hp1 | a0002 | c0011 | t0004 | g0007 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0164 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04184 | hp2 | a0010 | c0021 | t0001 | g0029 | SAS | BEB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04199 | hp1 | a0018 | c0039 | t0001 | g0040 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04199 | hp2 | a0002 | c0003 | t0003 | g0028 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0126 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0188 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18522 | hp1 | a0002 | c0003 | t0007 | g0236 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18522 | hp2 | a0005 | c0015 | t0011 | g0171 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | CHB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | CHB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18747 | hp2 | a0001 | c0052 | t0001 | g0153 | EAS | CHB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18906 | hp1 | a0002 | c0002 | t0013 | g0165 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18906 | hp2 | a0029 | c0028 | t0010 | g0179 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0257 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18939 | hp2 | a0002 | c0008 | t0004 | g0324 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18941 | hp1 | a0002 | c0004 | t0005 | g0232 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18943 | hp1 | a0002 | c0004 | t0005 | g0156 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0132 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18944 | hp2 | a0002 | c0003 | t0003 | g0134 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18945 | hp2 | a0001 | c0009 | t0014 | g0083 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18947 | hp1 | a0002 | c0004 | t0031 | g0279 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18950 | hp2 | a0002 | c0002 | t0018 | g0109 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18951 | hp1 | a0002 | c0004 | t0003 | g0149 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0074 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0247 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18954 | hp2 | a0001 | c0006 | t0002 | g0155 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0073 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18961 | hp2 | a0001 | c0001 | t0024 | g0105 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18966 | hp2 | a0002 | c0002 | t0018 | g0163 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0095 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0094 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18971 | hp2 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18980 | hp1 | a0002 | c0004 | t0033 | g0090 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0248 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0080 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18984 | hp2 | a0002 | c0004 | t0005 | g0280 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0204 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18994 | hp2 | a0002 | c0038 | t0004 | g0068 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18995 | hp1 | a0002 | c0022 | t0003 | g0147 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18999 | hp1 | a0023 | c0036 | t0001 | g0110 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19004 | hp1 | a0002 | c0008 | t0004 | g0065 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19011 | hp2 | a0002 | c0003 | t0003 | g0102 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19012 | hp1 | a0002 | c0004 | t0003 | g0161 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19012 | hp2 | a0002 | c0003 | t0003 | g0104 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19030 | hp2 | a0002 | c0003 | t0019 | g0186 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19056 | hp1 | a0002 | c0002 | t0004 | g0203 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19056 | hp2 | a0001 | c0006 | t0001 | g0282 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19062 | hp1 | a0030 | c0050 | t0001 | g0112 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19062 | hp2 | a0001 | c0013 | t0001 | g0146 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19064 | hp1 | a0002 | c0008 | t0004 | g0304 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19064 | hp2 | a0002 | c0022 | t0003 | g0148 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19065 | hp1 | a0026 | c0030 | t0030 | g0303 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19068 | hp2 | a0001 | c0009 | t0004 | g0013 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19070 | hp2 | a0001 | c0009 | t0002 | g0114 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19077 | hp2 | a0002 | c0003 | t0005 | g0103 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19079 | hp2 | a0002 | c0008 | t0032 | g0305 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19080 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19084 | hp1 | a0002 | c0008 | t0004 | g0296 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19087 | hp1 | a0016 | c0051 | t0002 | g0276 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19087 | hp2 | a0001 | c0013 | t0001 | g0150 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19090 | hp2 | a0020 | c0044 | t0005 | g0281 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19091 | hp1 | a0002 | c0003 | t0003 | g0141 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19091 | hp2 | a0002 | c0002 | t0004 | g0093 | EAS | JPT | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0237 | AFR | YRI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20129 | hp1 | a0002 | c0002 | t0004 | g0187 | AFR | ASW | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0372 | AFR | ASW | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0346 | EUR | TSI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20805 | hp1 | a0002 | c0004 | t0005 | g0054 | EUR | TSI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20805 | hp2 | a0004 | c0007 | t0001 | g0212 | EUR | TSI | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0211 | SAS | GIH | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20905 | hp2 | a0002 | c0003 | t0006 | g0335 | SAS | GIH | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0064 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG01123 | hp2 | a0003 | c0005 | t0001 | g0034 | AMR | CLM | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02109 | hp1 | a0006 | c0014 | t0009 | g0302 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0361 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02486 | hp1 | a0002 | c0003 | t0003 | g0289 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0321 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0243 | AFR | ACB | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03471 | hp1 | a0021 | c0034 | t0009 | g0287 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG03471 | hp2 | a0002 | c0003 | t0007 | g0315 | AFR | MSL | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG06807 | hp1 | a0005 | c0015 | t0011 | g0288 | AFR | USA | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| HG06807 | hp2 | a0008 | c0027 | t0017 | g0008 | AFR | USA | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0223 | AFR | USA | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA20300 | hp2 | a0003 | c0005 | t0001 | g0152 | AFR | USA | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0033 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | LWK | FLT4_chr5_180596506_180654600 | FLT4 | chr5 | 180596506 | 180654600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180603278
|
C | T | 1 | a0023 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.4006G>A | p.Glu1336Lys | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 4061/5833 | 4006/4092 | 1336/1363 | chr5 | 180603278 | ||
| chr5:180603313
|
C | A | 4 | a0003a0007a0019others(1): Show | 15 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(12): Show |
missense_variant | MODERATE | c.3971G>T | p.Arg1324Leu | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 4026/5833 | 3971/4092 | 1324/1363 | chr5 | 180603313 | ||
| chr5:180603325
|
C | T | 2 | a0005a0011 | 7 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
missense_variant | MODERATE | c.3959G>A | p.Arg1320Gln | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 4014/5833 | 3959/4092 | 1320/1363 | chr5 | 180603325 | ||
| chr5:180612583
|
C | T | 3 | a0006a0021a0024 | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.3460G>A | p.Gly1154Arg | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/30 | 3515/5833 | 3460/4092 | 1154/1363 | chr5 | 180612583 | ||
| chr5:180612606
|
C | T | 3 | a0004a0012a0031 | 9 | HG00140.hp2 HG00735.hp2 HG01175.hp1 others(6): Show |
missense_variant | MODERATE | c.3437G>A | p.Arg1146His | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/30 | 3492/5833 | 3437/4092 | 1146/1363 | chr5 | 180612606 | ||
| chr5:180613036
|
C | A | 1 | a0019 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.3406G>T | p.Ala1136Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 25/30 | 3461/5833 | 3406/4092 | 1136/1363 | chr5 | 180613036 | ||
| chr5:180618911
|
G | A | 1 | a0022 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.2860C>T | p.Pro954Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/30 | 2915/5833 | 2860/4092 | 954/1363 | chr5 | 180618911 | ||
| chr5:180619259
|
G | A | 1 | a0025 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.2755C>T | p.Pro919Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 19/30 | 2810/5833 | 2755/4092 | 919/1363 | chr5 | 180619259 | ||
| chr5:180619344
|
G | C | 17 | a0001a0003a0004others(14): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
missense_variant | MODERATE | c.2670C>G | p.His890Gln | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 19/30 | 2725/5833 | 2670/4092 | 890/1363 | chr5 | 180619344 | ||
| chr5:180620305
|
C | T | 1 | a0016 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.2410G>A | p.Ala804Thr | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/30 | 2465/5833 | 2410/4092 | 804/1363 | chr5 | 180620305 | ||
| chr5:180621737
|
C | G | 1 | a0026 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.1825G>C | p.Asp609His | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 13/30 | 1880/5833 | 1825/4092 | 609/1363 | chr5 | 180621737 | ||
| chr5:180621787
|
C | G | 1 | a0020 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1775G>C | p.Arg592Pro | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 13/30 | 1830/5833 | 1775/4092 | 592/1363 | chr5 | 180621787 | ||
| chr5:180622808
|
T | C | 2 | a0013a0014 | 4 | HG02145.hp2 HG02572.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.1580A>G | p.Asn527Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/30 | 1635/5833 | 1580/4092 | 527/1363 | chr5 | 180622808 | ||
| chr5:180624003
|
T | C | 5 | a0003a0010a0018others(2): Show | 14 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(11): Show |
missense_variant | MODERATE | c.1480A>G | p.Thr494Ala | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/30 | 1535/5833 | 1480/4092 | 494/1363 | chr5 | 180624003 | ||
| chr5:180628936
|
T | A | 1 | a0027 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1049A>T | p.Glu350Val | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/30 | 1104/5833 | 1049/4092 | 350/1363 | chr5 | 180628936 | ||
| chr5:180630254
|
T | C | 1 | a0028 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.484A>G | p.Ile162Val | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/30 | 539/5833 | 484/4092 | 162/1363 | chr5 | 180630254 | ||
| chr5:180630293
|
T | C | 4 | a0004a0009a0017others(1): Show | 10 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(7): Show |
missense_variant | MODERATE | c.445A>G | p.Asn149Asp | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/30 | 500/5833 | 445/4092 | 149/1363 | chr5 | 180630293 | ||
| chr5:180630594
|
C | T | 1 | a0029 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.361G>A | p.Glu121Lys | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/30 | 416/5833 | 361/4092 | 121/1363 | chr5 | 180630594 | ||
| chr5:180630692
|
T | A | 1 | a0030 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.263A>T | p.Asp88Val | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/30 | 318/5833 | 263/4092 | 88/1363 | chr5 | 180630692 | ||
| chr5:180630723
|
T | A | 1 | a0016 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.232A>T | p.Thr78Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/30 | 287/5833 | 232/4092 | 78/1363 | chr5 | 180630723 | ||
| chr5:180631761
|
A | C | 2 | a0008a0015 | 3 | HG02451.hp2 HG03516.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.76T>G | p.Ser26Ala | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/30 | 131/5833 | 76/4092 | 26/1363 | chr5 | 180631761 | ||
| chr5:180649533
|
C | A | 1 | a0031 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.13G>T | p.Ala5Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/30 | 68/5833 | 13/4092 | 5/1363 | chr5 | 180649533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180603321
|
C | T | 1 | a0002c0035 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.3963G>A | p.Arg1321Arg | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 4018/5833 | 3963/4092 | 1321/1363 | chr5 | 180603321 | ||
| chr5:180608994
|
G | A | 1 | a0005c0015 | 3 | HG02572.hp1 HG06807.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.3867C>T | p.Ser1289Ser | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/30 | 3922/5833 | 3867/4092 | 1289/1363 | chr5 | 180608994 | ||
| chr5:180616388
|
G | A | 14 | a0001c0009a0001c0023a0002c0002others(11): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(91): Show |
synonymous_variant | LOW | c.3198C>T | p.Pro1066Pro | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/30 | 3253/5833 | 3198/4092 | 1066/1363 | chr5 | 180616388 | ||
| chr5:180616439
|
G | A | 1 | a0002c0012 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.3147C>T | p.Asp1049Asp | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/30 | 3202/5833 | 3147/4092 | 1049/1363 | chr5 | 180616439 | ||
| chr5:180620669
|
G | C | 1 | a0002c0038 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.2346C>G | p.Thr782Thr | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 16/30 | 2401/5833 | 2346/4092 | 782/1363 | chr5 | 180620669 | ||
| chr5:180620976
|
C | T | 1 | a0001c0032 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2199G>A | p.Leu733Leu | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/30 | 2254/5833 | 2199/4092 | 733/1363 | chr5 | 180620976 | ||
| chr5:180620979
|
C | T | 2 | a0002c0008a0026c0030 | 6 | NA18939.hp2 NA19004.hp1 NA19064.hp1 others(3): Show |
synonymous_variant | LOW | c.2196G>A | p.Lys732Lys | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/30 | 2251/5833 | 2196/4092 | 732/1363 | chr5 | 180620979 | ||
| chr5:180621128
|
C | T | 1 | a0001c0031 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.2145G>A | p.Glu715Glu | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 14/30 | 2200/5833 | 2145/4092 | 715/1363 | chr5 | 180621128 | ||
| chr5:180624010
|
C | T | 1 | a0002c0029 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.1473G>A | p.Ala491Ala | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/30 | 1528/5833 | 1473/4092 | 491/1363 | chr5 | 180624010 | ||
| chr5:180625946
|
G | A | 5 | a0001c0013a0002c0004a0002c0041others(2): Show | 23 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
synonymous_variant | LOW | c.1344C>T | p.Tyr448Tyr | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/30 | 1399/5833 | 1344/4092 | 448/1363 | chr5 | 180625946 | ||
| chr5:180629404
|
G | A | 1 | a0008c0027 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.840C>T | p.Pro280Pro | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 7/30 | 895/5833 | 840/4092 | 280/1363 | chr5 | 180629404 | ||
| chr5:180629986
|
T | C | 2 | a0001c0047a0005c0015 | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
synonymous_variant | LOW | c.633A>G | p.Gly211Gly | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 5/30 | 688/5833 | 633/4092 | 211/1363 | chr5 | 180629986 | ||
| chr5:180630043
|
G | A | 1 | a0001c0043 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.576C>T | p.Leu192Leu | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 5/30 | 631/5833 | 576/4092 | 192/1363 | chr5 | 180630043 | ||
| chr5:180630231
|
C | A | 8 | a0001c0006a0001c0013a0001c0052others(5): Show | 35 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
synonymous_variant | LOW | c.507G>T | p.Leu169Leu | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/30 | 562/5833 | 507/4092 | 169/1363 | chr5 | 180630231 | ||
| chr5:180630249
|
G | A | 5 | a0001c0023a0001c0047a0005c0015others(2): Show | 10 | HG01167.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
synonymous_variant | LOW | c.489C>T | p.Pro163Pro | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/30 | 544/5833 | 489/4092 | 163/1363 | chr5 | 180630249 | ||
| chr5:180631708
|
G | A | 1 | a0001c0052 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.129C>T | p.Thr43Thr | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/30 | 184/5833 | 129/4092 | 43/1363 | chr5 | 180631708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180601509
|
G | A | 13 | a0001c0001t0005a0002c0002t0005a0002c0003t0005others(10): Show | 28 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1683C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1683 | chr5 | 180601509 | |||||
| chr5:180601562
|
T | TTCGATCT others(15): Show |
1 | a0002c0002t0022 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1608_*1629dupCCAT others(18): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1629 | chr5 | 180601562 | |||||
| chr5:180601586
|
C | G | 1 | a0001c0001t0029 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1606G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1606 | chr5 | 180601586 | |||||
| chr5:180601677
|
T | C | 25 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(22): Show | 42 | HG01192.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1515A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1515 | chr5 | 180601677 | |||||
| chr5:180601717
|
T | C | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(64): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*1475A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1475 | chr5 | 180601717 | |||||
| chr5:180601727
|
G | T | 5 | a0002c0003t0007a0008c0025t0017a0008c0027t0017others(2): Show | 13 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1465C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1465 | chr5 | 180601727 | |||||
| chr5:180601734
|
G | A | 1 | a0002c0002t0018 | 2 | NA18950.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1458C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1458 | chr5 | 180601734 | |||||
| chr5:180601743
|
C | T | 31 | a0001c0001t0004a0001c0001t0008a0001c0001t0015others(28): Show | 68 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1449G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1449 | chr5 | 180601743 | |||||
| chr5:180601792
|
C | T | 1 | a0002c0012t0021 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1400G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1400 | chr5 | 180601792 | |||||
| chr5:180602048
|
G | C | 3 | a0005c0015t0011a0005c0018t0011a0011c0016t0011 | 5 | HG02258.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1144C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 1144 | chr5 | 180602048 | |||||
| chr5:180602225
|
A | C | 1 | a0001c0032t0026 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 967 | chr5 | 180602225 | |||||
| chr5:180602319
|
C | A | 1 | a0001c0001t0012 | 5 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*873G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 873 | chr5 | 180602319 | |||||
| chr5:180602398
|
C | T | 1 | a0001c0001t0025 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 794 | chr5 | 180602398 | |||||
| chr5:180602458
|
C | T | 8 | a0001c0001t0008a0001c0001t0020a0001c0023t0008others(5): Show | 11 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*734G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 734 | chr5 | 180602458 | |||||
| chr5:180602471
|
C | G | 25 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(22): Show | 77 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*721G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 721 | chr5 | 180602471 | |||||
| chr5:180602614
|
T | C | 1 | a0026c0030t0030 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 578 | chr5 | 180602614 | |||||
| chr5:180602616
|
G | A | 19 | a0001c0001t0005a0001c0001t0008a0001c0001t0016others(16): Show | 37 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 576 | chr5 | 180602616 | |||||
| chr5:180602670
|
A | T | 8 | a0001c0001t0008a0001c0001t0020a0001c0023t0008others(5): Show | 11 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*522T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 522 | chr5 | 180602670 | |||||
| chr5:180602724
|
T | C | 1 | a0002c0003t0019 | 2 | HG02895.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*468A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 468 | chr5 | 180602724 | |||||
| chr5:180602746
|
G | C | 1 | a0002c0004t0031 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 446 | chr5 | 180602746 | |||||
| chr5:180602879
|
G | A | 12 | a0001c0001t0005a0001c0001t0016a0001c0031t0016others(9): Show | 27 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*313C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 313 | chr5 | 180602879 | |||||
| chr5:180603132
|
C | T | 10 | a0001c0001t0008a0001c0001t0020a0001c0023t0008others(7): Show | 13 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*60G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 30/30 | 60 | chr5 | 180603132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180603487
|
G | A | 1 | a0002c0002t0004g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3894-97C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603487 | ||||||
| chr5:180603519
|
C | T | 26 | a0001c0001t0005g0079a0001c0001t0005g0117a0001c0001t0016g0023others(23): Show | 26 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.3894-129G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603519 | ||||||
| chr5:180603531
|
G | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3894-141C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603531 | ||||||
| chr5:180603541
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3894-151C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603541 | ||||||
| chr5:180603549
|
A | G | 2 | a0002c0002t0013g0165a0002c0003t0001g0370 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3894-159T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603549 | ||||||
| chr5:180603577
|
T | G | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3894-187A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603577 | ||||||
| chr5:180603629
|
C | T | 1 | a0014c0020t0013g0271 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3894-239G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603629 | ||||||
| chr5:180603671
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3894-281C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603671 | ||||||
| chr5:180603692
|
C | T | 2 | a0002c0011t0004g0007a0002c0011t0014g0166 | 3 | HG02735.hp1 HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3894-302G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603692 | ||||||
| chr5:180603711
|
T | C | 47 | a0001c0001t0004g0078a0001c0001t0004g0087a0001c0001t0004g0131others(44): Show | 48 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.3894-321A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603711 | ||||||
| chr5:180603715
|
T | C | 3 | a0002c0003t0010g0043a0002c0003t0010g0178a0029c0028t0010g0179 | 3 | HG02647.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3894-325A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603715 | ||||||
| chr5:180603765
|
G | A | 6 | a0002c0003t0003g0077a0002c0003t0003g0102a0002c0003t0003g0134others(3): Show | 6 | HG02080.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.3894-375C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603765 | ||||||
| chr5:180603826
|
C | A | 2 | a0002c0002t0013g0165a0002c0003t0001g0370 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3894-436G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603826 | ||||||
| chr5:180603858
|
C | T | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3894-468G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603858 | ||||||
| chr5:180603861
|
A | G | 44 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(41): Show | 44 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.3894-471T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603861 | ||||||
| chr5:180603883
|
G | A | 2 | a0002c0002t0013g0165a0002c0003t0001g0370 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3894-493C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603883 | ||||||
| chr5:180603884
|
A | T | 85 | a0001c0001t0001g0261a0001c0001t0004g0078a0001c0001t0004g0087others(82): Show | 87 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3894-494T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603884 | ||||||
| chr5:180603903
|
T | TA | 125 | a0001c0001t0001g0261a0001c0001t0001g0365a0001c0001t0002g0239others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.3894-514dupT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603903 | ||||||
| chr5:180603903
|
T | TAAAAA | 39 | a0002c0003t0002g0286a0002c0003t0002g0325a0002c0003t0002g0336others(36): Show | 40 | HG00673.hp2 HG01891.hp2 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.3894-518_3894-514d others(7): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603903 | ||||||
| chr5:180603903
|
TA | T | 7 | a0001c0001t0001g0092a0001c0001t0001g0215a0001c0001t0001g0319others(4): Show | 7 | HG01257.hp2 HG01517.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3894-514delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603903 | ||||||
| chr5:180603986
|
C | A | 1 | a0001c0001t0002g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3894-596G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603986 | ||||||
| chr5:180603996
|
C | A | 43 | a0002c0002t0022g0313a0002c0003t0002g0286a0002c0003t0002g0325others(40): Show | 44 | HG00597.hp1 HG00673.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.3894-606G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180603996 | ||||||
| chr5:180604086
|
G | T | 14 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(11): Show | 14 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3894-696C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604086 | ||||||
| chr5:180604093
|
G | A | 1 | a0005c0015t0011g0171 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3894-703C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604093 | ||||||
| chr5:180604125
|
C | T | 2 | a0007c0010t0010g0323a0007c0010t0015g0044 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3894-735G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604125 | ||||||
| chr5:180604131
|
C | T | 38 | a0001c0001t0001g0261a0001c0009t0001g0019a0001c0009t0001g0063others(35): Show | 39 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.3894-741G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604131 | ||||||
| chr5:180604263
|
C | T | 1 | a0002c0011t0004g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3894-873G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604263 | ||||||
| chr5:180604264
|
G | A | 2 | a0002c0003t0003g0274a0002c0004t0031g0279 | 2 | HG02129.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.3894-874C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604264 | ||||||
| chr5:180604278
|
C | T | 3 | a0007c0010t0010g0323a0007c0010t0015g0044a0007c0010t0015g0252 | 3 | HG01243.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3894-888G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604278 | ||||||
| chr5:180604367
|
A | G | 128 | a0001c0001t0001g0261a0001c0001t0001g0299a0001c0001t0004g0078others(125): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.3894-977T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604367 | ||||||
| chr5:180604412
|
C | T | 25 | a0001c0001t0005g0079a0001c0001t0005g0117a0001c0001t0016g0023others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.3894-1022G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604412 | ||||||
| chr5:180604519
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3894-1129C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604519 | ||||||
| chr5:180604547
|
C | T | 1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3894-1157G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604547 | ||||||
| chr5:180604565
|
C | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3894-1175G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604565 | ||||||
| chr5:180604784
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3894-1394G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604784 | ||||||
| chr5:180604787
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3894-1397G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604787 | ||||||
| chr5:180604789
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3894-1399A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604789 | ||||||
| chr5:180604864
|
T | G | 1 | a0002c0002t0001g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3894-1474A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604864 | ||||||
| chr5:180604884
|
G | A | 1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3894-1494C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604884 | ||||||
| chr5:180604966
|
G | T | 1 | a0001c0052t0001g0153 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3894-1576C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604966 | ||||||
| chr5:180604980
|
A | G | 9 | a0001c0001t0001g0091a0001c0001t0001g0133a0001c0001t0001g0135others(6): Show | 9 | NA18945.hp1 NA18947.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.3894-1590T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180604980 | ||||||
| chr5:180605043
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3894-1653G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605043 | ||||||
| chr5:180605045
|
C | T | 13 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(10): Show | 13 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3894-1655G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605045 | ||||||
| chr5:180605182
|
C | G | 1 | a0001c0006t0001g0359 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3894-1792G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605182 | ||||||
| chr5:180605226
|
G | A | 135 | a0001c0001t0001g0039a0001c0001t0001g0365a0001c0001t0004g0078others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.3894-1836C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605226 | ||||||
| chr5:180605240
|
C | T | 2 | a0002c0003t0002g0325a0002c0003t0002g0336 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3894-1850G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605240 | ||||||
| chr5:180605263
|
G | A | 82 | a0001c0001t0004g0078a0001c0001t0004g0087a0001c0001t0004g0131others(79): Show | 84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3894-1873C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605263 | ||||||
| chr5:180605291
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3894-1901G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605291 | ||||||
| chr5:180605294
|
A | T | 1 | a0009c0024t0001g0004 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3894-1904T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605294 | ||||||
| chr5:180605428
|
T | C | 1 | a0002c0003t0006g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3894-2038A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605428 | ||||||
| chr5:180605449
|
A | G | 1 | a0002c0002t0001g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3894-2059T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605449 | ||||||
| chr5:180605500
|
G | C | 9 | a0004c0007t0001g0010a0004c0007t0001g0015a0004c0007t0001g0017others(6): Show | 9 | HG00140.hp2 HG00735.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.3894-2110C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605500 | ||||||
| chr5:180605536
|
C | A | 1 | a0014c0020t0013g0271 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3894-2146G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605536 | ||||||
| chr5:180605684
|
C | G | 25 | a0001c0001t0005g0079a0001c0001t0005g0117a0001c0001t0016g0023others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.3894-2294G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605684 | ||||||
| chr5:180605885
|
A | G | 173 | a0001c0001t0001g0365a0001c0001t0004g0078a0001c0001t0004g0087others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.3894-2495T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605885 | ||||||
| chr5:180605934
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3894-2544G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605934 | ||||||
| chr5:180605942
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3894-2552C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180605942 | ||||||
| chr5:180606010
|
A | C | 177 | a0001c0001t0001g0365a0001c0001t0004g0078a0001c0001t0004g0087others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.3894-2620T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606010 | ||||||
| chr5:180606031
|
G | A | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0002c0002t0001g0002others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3894-2641C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606031 | ||||||
| chr5:180606148
|
C | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3894-2758G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606148 | ||||||
| chr5:180606246
|
T | C | 12 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3893+2722A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606246 | ||||||
| chr5:180606264
|
C | CCAAGCAT others(11): Show |
3 | a0001c0001t0002g0307a0001c0001t0002g0371a0001c0001t0002g0372 | 3 | HG01952.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3893+2686_3893+270 others(22): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606264 | ||||||
| chr5:180606292
|
C | T | 79 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(76): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3893+2676G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606292 | ||||||
| chr5:180606360
|
C | T | 8 | a0002c0003t0003g0077a0002c0003t0003g0102a0002c0003t0003g0108others(5): Show | 8 | HG00673.hp2 HG01975.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.3893+2608G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606360 | ||||||
| chr5:180606377
|
C | T | 2 | a0002c0012t0021g0174a0002c0012t0023g0045 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3893+2591G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606377 | ||||||
| chr5:180606438
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3893+2530C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606438 | ||||||
| chr5:180606440
|
C | T | 1 | a0006c0014t0009g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3893+2528G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606440 | ||||||
| chr5:180606485
|
G | A | 1 | a0002c0002t0001g0339 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3893+2483C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606485 | ||||||
| chr5:180606550
|
T | C | 2 | a0003c0005t0001g0175a0003c0005t0001g0176 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3893+2418A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606550 | ||||||
| chr5:180606605
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3893+2363A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606605 | ||||||
| chr5:180606627
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3893+2341C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606627 | ||||||
| chr5:180606633
|
T | C | 126 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.3893+2335A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606633 | ||||||
| chr5:180606639
|
T | C | 126 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.3893+2329A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606639 | ||||||
| chr5:180606738
|
G | A | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3893+2230C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606738 | ||||||
| chr5:180606763
|
G | A | 1 | a0002c0012t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3893+2205C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606763 | ||||||
| chr5:180606829
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3893+2139C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606829 | ||||||
| chr5:180606877
|
G | A | 113 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3893+2091C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606877 | ||||||
| chr5:180606901
|
A | C | 112 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3893+2067T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606901 | ||||||
| chr5:180606904
|
A | AAC | 200 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(197): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.3893+2063_3893+206 others(6): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606904 | ||||||
| chr5:180606904
|
A | AC | 4 | a0001c0001t0001g0319a0001c0001t0002g0216a0001c0001t0002g0217others(1): Show | 4 | HG01257.hp2 NA18941.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.3893+2063_3893+206 others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606904 | ||||||
| chr5:180606904
|
A | C | 2 | a0001c0001t0012g0357a0002c0002t0001g0115 | 2 | HG00280.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3893+2064T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606904 | ||||||
| chr5:180606906
|
A | C | 112 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3893+2062T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606906 | ||||||
| chr5:180606908
|
A | C | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3893+2060T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606908 | ||||||
| chr5:180606909
|
A | C | 13 | a0001c0001t0012g0005a0001c0001t0012g0223a0001c0001t0012g0357others(10): Show | 14 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.3893+2059T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606909 | ||||||
| chr5:180606911
|
A | C | 112 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(109): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3893+2057T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606911 | ||||||
| chr5:180606912
|
A | C | 8 | a0001c0001t0001g0277a0001c0001t0002g0306a0001c0001t0006g0188others(5): Show | 8 | HG01109.hp1 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.3893+2056T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606912 | ||||||
| chr5:180606916
|
C | A | 19 | a0001c0001t0001g0039a0001c0001t0008g0144a0001c0001t0012g0005others(16): Show | 20 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.3893+2052G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606916 | ||||||
| chr5:180606916
|
C | CAAA | 34 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.3893+2049_3893+205 others(7): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606916 | ||||||
| chr5:180606916
|
C | CAAAA | 77 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(74): Show | 79 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.3893+2051_3893+205 others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606916 | ||||||
| chr5:180606920
|
C | A | 126 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.3893+2048G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606920 | ||||||
| chr5:180606924
|
C | A | 13 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(10): Show | 13 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3893+2044G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606924 | ||||||
| chr5:180606953
|
C | T | 80 | a0001c0001t0020g0361a0001c0009t0001g0019a0001c0009t0001g0063others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3893+2015G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606953 | ||||||
| chr5:180606994
|
C | T | 3 | a0001c0001t0002g0310a0001c0001t0002g0311a0001c0001t0002g0312 | 3 | HG02723.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3893+1974G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180606994 | ||||||
| chr5:180607102
|
T | C | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1866A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607102 | ||||||
| chr5:180607177
|
G | C | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1791C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607177 | ||||||
| chr5:180607237
|
G | A | 79 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(76): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3893+1731C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607237 | ||||||
| chr5:180607374
|
G | A | 2 | a0002c0012t0021g0174a0002c0012t0023g0045 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3893+1594C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607374 | ||||||
| chr5:180607374
|
G | C | 113 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(110): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3893+1594C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607374 | ||||||
| chr5:180607376
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3893+1592G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607376 | ||||||
| chr5:180607379
|
G | A | 11 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(8): Show | 11 | HG01167.hp1 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3893+1589C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607379 | ||||||
| chr5:180607453
|
T | C | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1515A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607453 | ||||||
| chr5:180607454
|
G | A | 1 | a0002c0004t0005g0280 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3893+1514C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607454 | ||||||
| chr5:180607456
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3893+1512G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607456 | ||||||
| chr5:180607463
|
C | T | 1 | a0002c0003t0001g0375 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3893+1505G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607463 | ||||||
| chr5:180607464
|
G | C | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1504C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607464 | ||||||
| chr5:180607513
|
T | C | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1455A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607513 | ||||||
| chr5:180607536
|
A | G | 114 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3893+1432T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607536 | ||||||
| chr5:180607584
|
C | T | 128 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.3893+1384G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607584 | ||||||
| chr5:180607619
|
A | T | 80 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3893+1349T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607619 | ||||||
| chr5:180607628
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3893+1340C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607628 | ||||||
| chr5:180607638
|
C | CA | 123 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.3893+1329dupT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607638 | ||||||
| chr5:180607638
|
CA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(106): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.3893+1329delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607638 | ||||||
| chr5:180607659
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3893+1309T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607659 | ||||||
| chr5:180607662
|
C | CAT | 117 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(114): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.3893+1304_3893+130 others(6): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607662 | ||||||
| chr5:180607662
|
C | CATAT | 11 | a0001c0001t0020g0361a0002c0002t0001g0256a0002c0003t0001g0370others(8): Show | 11 | HG01167.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3893+1302_3893+130 others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607662 | ||||||
| chr5:180607823
|
T | C | 115 | a0001c0001t0001g0365a0001c0001t0005g0079a0001c0001t0005g0117others(112): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3893+1145A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607823 | ||||||
| chr5:180607900
|
G | GC | 12 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3893+1067dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607900 | ||||||
| chr5:180607902
|
A | C | 12 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3893+1066T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607902 | ||||||
| chr5:180607940
|
G | T | 1 | a0002c0002t0001g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3893+1028C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607940 | ||||||
| chr5:180607962
|
G | A | 6 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | NA18945.hp1 NA18947.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.3893+1006C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607962 | ||||||
| chr5:180607977
|
A | G | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3893+991T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180607977 | ||||||
| chr5:180608069
|
G | A | 27 | a0002c0003t0002g0325a0002c0003t0002g0336a0002c0003t0003g0028others(24): Show | 27 | HG00597.hp1 HG00673.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.3893+899C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608069 | ||||||
| chr5:180608182
|
CAGT | C | 22 | a0001c0001t0005g0079a0001c0001t0005g0117a0002c0003t0005g0103others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.3893+783_3893+785d others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608182 | ||||||
| chr5:180608347
|
C | T | 81 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3893+621G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608347 | ||||||
| chr5:180608412
|
C | T | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3893+556G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608412 | ||||||
| chr5:180608471
|
C | T | 7 | a0001c0001t0001g0365a0001c0047t0001g0173a0005c0015t0011g0171others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3893+497G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608471 | ||||||
| chr5:180608504
|
C | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3893+464G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608504 | ||||||
| chr5:180608513
|
A | G | 12 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3893+455T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608513 | ||||||
| chr5:180608524
|
C | T | 1 | a0002c0003t0019g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3893+444G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608524 | ||||||
| chr5:180608556
|
G | A | 3 | a0002c0008t0004g0304a0002c0008t0032g0305a0026c0030t0030g0303 | 3 | NA19064.hp1 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3893+412C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608556 | ||||||
| chr5:180608608
|
A | C | 1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3893+360T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608608 | ||||||
| chr5:180608663
|
A | G | 1 | a0002c0002t0004g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3893+305T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608663 | ||||||
| chr5:180608676
|
T | A | 1 | a0001c0006t0001g0282 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3893+292A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608676 | ||||||
| chr5:180608730
|
A | G | 7 | a0001c0001t0001g0365a0001c0047t0001g0173a0005c0015t0011g0171others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3893+238T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608730 | ||||||
| chr5:180608744
|
T | C | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3893+224A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608744 | ||||||
| chr5:180608792
|
C | T | 11 | a0001c0001t0001g0299a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 11 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3893+176G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608792 | ||||||
| chr5:180608795
|
G | A | 2 | a0002c0002t0001g0061a0002c0002t0001g0115 | 2 | NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3893+173C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608795 | ||||||
| chr5:180608842
|
G | A | 2 | a0002c0002t0003g0207a0027c0042t0028g0379 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3893+126C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608842 | ||||||
| chr5:180608873
|
G | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3893+95C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608873 | ||||||
| chr5:180608901
|
C | T | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3893+67G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608901 | ||||||
| chr5:180608947
|
G | A | 1 | a0002c0003t0003g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3893+21C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 29/29 | chr5 | 180608947 | ||||||
| chr5:180609230
|
C | A | 1 | a0001c0001t0004g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3808-177G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609230 | ||||||
| chr5:180609239
|
G | A | 53 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0009t0001g0019others(50): Show | 54 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.3808-186C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609239 | ||||||
| chr5:180609255
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3808-202C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609255 | ||||||
| chr5:180609318
|
A | G | 94 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0009t0001g0019others(91): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.3808-265T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609318 | ||||||
| chr5:180609323
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG02135.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3808-270G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609323 | ||||||
| chr5:180609484
|
G | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00438.hp1 NA18612.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.3807+421C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609484 | ||||||
| chr5:180609619
|
A | C | 1 | a0001c0013t0001g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3807+286T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609619 | ||||||
| chr5:180609750
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3807+155C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609750 | ||||||
| chr5:180609826
|
C | T | 1 | a0002c0003t0003g0362 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3807+79G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609826 | ||||||
| chr5:180609871
|
C | G | 40 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.3807+34G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609871 | ||||||
| chr5:180609872
|
G | A | 1 | a0001c0001t0027g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3807+33C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 28/29 | chr5 | 180609872 | ||||||
| chr5:180610190
|
C | A | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3687-165G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610190 | ||||||
| chr5:180610252
|
C | T | 1 | a0002c0002t0014g0031 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3687-227G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610252 | ||||||
| chr5:180610313
|
C | T | 7 | a0001c0001t0001g0365a0001c0047t0001g0173a0005c0015t0011g0171others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3687-288G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610313 | ||||||
| chr5:180610317
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(108): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.3687-292G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610317 | ||||||
| chr5:180610318
|
G | A | 23 | a0001c0001t0005g0079a0001c0001t0005g0117a0002c0003t0005g0103others(20): Show | 23 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.3687-293C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610318 | ||||||
| chr5:180610574
|
A | G | 2 | a0003c0005t0002g0042a0019c0040t0002g0046 | 2 | HG00642.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.3687-549T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610574 | ||||||
| chr5:180610628
|
C | T | 12 | a0001c0001t0008g0144a0001c0001t0020g0361a0001c0023t0008g0377others(9): Show | 12 | HG01167.hp1 HG01261.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3687-603G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610628 | ||||||
| chr5:180610644
|
T | A | 337 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(334): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.3687-619A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610644 | ||||||
| chr5:180610718
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3686+613C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610718 | ||||||
| chr5:180610773
|
G | A | 41 | a0001c0009t0001g0019a0001c0009t0001g0063a0002c0002t0001g0002others(38): Show | 42 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.3686+558C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610773 | ||||||
| chr5:180610823
|
C | T | 23 | a0001c0001t0005g0079a0001c0001t0005g0117a0002c0003t0005g0103others(20): Show | 23 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.3686+508G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610823 | ||||||
| chr5:180610829
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3686+502T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610829 | ||||||
| chr5:180610884
|
C | T | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3686+447G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610884 | ||||||
| chr5:180610918
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(202): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.3686+413C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610918 | ||||||
| chr5:180610928
|
G | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.3686+403C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610928 | ||||||
| chr5:180610929
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(330): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.3686+402A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610929 | ||||||
| chr5:180610940
|
C | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(330): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.3686+391G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610940 | ||||||
| chr5:180610988
|
C | G | 3 | a0002c0002t0001g0027a0002c0002t0001g0030a0002c0002t0001g0255 | 3 | HG00099.hp1 HG00280.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3686+343G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610988 | ||||||
| chr5:180610988
|
C | T | 78 | a0001c0001t0002g0066a0001c0009t0001g0019a0001c0009t0001g0063others(75): Show | 80 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.3686+343G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610988 | ||||||
| chr5:180610998
|
G | A | 80 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3686+333C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180610998 | ||||||
| chr5:180611043
|
C | T | 10 | a0001c0023t0008g0377a0001c0023t0008g0378a0006c0014t0002g0374others(7): Show | 10 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3686+288G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611043 | ||||||
| chr5:180611044
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3686+287C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611044 | ||||||
| chr5:180611052
|
G | A | 1 | a0001c0001t0015g0332 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3686+279C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611052 | ||||||
| chr5:180611064
|
T | A | 7 | a0001c0001t0027g0231a0001c0047t0001g0173a0004c0007t0001g0010others(4): Show | 7 | HG01978.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3686+267A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611064 | ||||||
| chr5:180611142
|
G | A | 10 | a0001c0023t0008g0377a0001c0023t0008g0378a0006c0014t0002g0374others(7): Show | 10 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3686+189C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611142 | ||||||
| chr5:180611145
|
G | A | 9 | a0001c0001t0001g0091a0001c0001t0001g0133a0001c0001t0001g0135others(6): Show | 9 | NA18945.hp1 NA18947.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.3686+186C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611145 | ||||||
| chr5:180611248
|
T | TC | 210 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.3686+82dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 27/29 | chr5 | 180611248 | ||||||
| chr5:180611545
|
A | G | 53 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.3538-66T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611545 | ||||||
| chr5:180611545
|
ACCCTCAG others(12): Show |
A | 1 | a0002c0003t0001g0317 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3538-85_3538-67del others(19): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611545 | ||||||
| chr5:180611585
|
C | A | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3538-106G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611585 | ||||||
| chr5:180611592
|
CCTCGCCC others(12): Show |
C | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3538-132_3538-114d others(21): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611592 | ||||||
| chr5:180611596
|
G | A | 1 | a0002c0003t0007g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3538-117C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611596 | ||||||
| chr5:180611627
|
G | A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3538-148C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611627 | ||||||
| chr5:180611678
|
CCT | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(199): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.3538-201_3538-200d others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611678 | ||||||
| chr5:180611696
|
C | T | 7 | a0002c0002t0001g0011a0002c0002t0001g0341a0002c0002t0001g0342others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.3538-217G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611696 | ||||||
| chr5:180611711
|
C | T | 8 | a0001c0001t0001g0365a0001c0047t0001g0173a0005c0015t0011g0171others(5): Show | 8 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3538-232G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611711 | ||||||
| chr5:180611887
|
C | T | 5 | a0001c0001t0002g0229a0001c0001t0002g0310a0001c0001t0002g0311others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3538-408G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611887 | ||||||
| chr5:180611979
|
C | T | 45 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(42): Show | 46 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.3538-500G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180611979 | ||||||
| chr5:180612028
|
C | T | 1 | a0002c0003t0013g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3537+478G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612028 | ||||||
| chr5:180612170
|
G | A | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3537+336C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612170 | ||||||
| chr5:180612187
|
A | G | 338 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(335): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.3537+319T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612187 | ||||||
| chr5:180612285
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3537+221T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612285 | ||||||
| chr5:180612328
|
C | A | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3537+178G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612328 | ||||||
| chr5:180612366
|
T | C | 1 | a0002c0002t0001g0346 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3537+140A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 26/29 | chr5 | 180612366 | ||||||
| chr5:180612639
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3432-28C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 25/29 | chr5 | 180612639 | ||||||
| chr5:180612807
|
C | T | 3 | a0001c0013t0001g0146a0001c0013t0001g0150a0001c0013t0001g0151 | 3 | HG00673.hp1 NA19062.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3432-196G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 25/29 | chr5 | 180612807 | ||||||
| chr5:180612828
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3431+183G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 25/29 | chr5 | 180612828 | ||||||
| chr5:180612877
|
C | T | 3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3431+134G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 25/29 | chr5 | 180612877 | ||||||
| chr5:180613296
|
C | T | 1 | a0001c0001t0006g0344 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3332-186G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613296 | ||||||
| chr5:180613411
|
C | T | 2 | a0002c0002t0001g0089a0002c0035t0001g0221 | 2 | HG02015.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3332-301G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613411 | ||||||
| chr5:180613457
|
T | C | 339 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(336): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.3332-347A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613457 | ||||||
| chr5:180613470
|
T | TCCTGCTG others(88): Show |
1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3332-361_3332-360i others(97): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613470 | ||||||
| chr5:180613470
|
TCCTGCTG others(12): Show |
T | 3 | a0001c0001t0002g0216a0001c0001t0002g0217a0002c0012t0001g0052 | 3 | HG02886.hp2 NA18941.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3332-379_3332-361d others(21): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613470 | ||||||
| chr5:180613475
|
C | T | 6 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(3): Show | 6 | HG02647.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3332-365G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613475 | ||||||
| chr5:180613494
|
C | T | 1 | a0002c0012t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3332-384G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613494 | ||||||
| chr5:180613503
|
C | A | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3332-393G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613503 | ||||||
| chr5:180613540
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3332-430G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613540 | ||||||
| chr5:180613636
|
C | T | 91 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(88): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.3331+432G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613636 | ||||||
| chr5:180613639
|
G | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3331+429C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613639 | ||||||
| chr5:180613724
|
G | T | 22 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.3331+344C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613724 | ||||||
| chr5:180613740
|
T | C | 2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3331+328A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613740 | ||||||
| chr5:180613842
|
T | G | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3331+226A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613842 | ||||||
| chr5:180613887
|
C | T | 2 | a0001c0001t0001g0360a0001c0001t0010g0368 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3331+181G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613887 | ||||||
| chr5:180613918
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(115): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.3331+150C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613918 | ||||||
| chr5:180613954
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3331+114G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613954 | ||||||
| chr5:180613982
|
G | A | 1 | a0002c0011t0004g0007 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3331+86C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180613982 | ||||||
| chr5:180614001
|
G | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(335): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.3331+67C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180614001 | ||||||
| chr5:180614008
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(325): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.3331+60A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 24/29 | chr5 | 180614008 | ||||||
| chr5:180614180
|
C | CTGGGGAG others(197): Show |
2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
splice_acceptor_variant&intron_variant | HIGH | c.3220-2_3220-1insTC others(202): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614180 | ||||||
| chr5:180614180
|
CTGGGGAG others(27): Show |
C | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3220-35_3220-2delT others(33): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614180 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(27): Show |
1 | a0001c0001t0010g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3220-22_3220-21ins others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(27): Show |
209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(206): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.3220-22_3220-21ins others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(197): Show |
2 | a0002c0002t0003g0207a0027c0042t0028g0379 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3220-22_3220-21ins others(204): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(197): Show |
42 | a0001c0009t0004g0013a0001c0009t0014g0083a0002c0002t0001g0027others(39): Show | 43 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.3220-22_3220-21ins others(204): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(673): Show |
1 | a0001c0009t0002g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3220-22_3220-21ins others(680): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614200
|
T | TTGTCCCG others(231): Show |
1 | a0026c0030t0030g0303 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3220-22_3220-21ins others(238): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614200 | ||||||
| chr5:180614203
|
T | TCCCGCGG others(28): Show |
1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3220-25_3220-24ins others(35): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614203 | ||||||
| chr5:180614206
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-27G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614206 | ||||||
| chr5:180614208
|
T | C | 36 | a0001c0001t0002g0066a0001c0001t0005g0117a0001c0001t0008g0144others(33): Show | 36 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.3220-29A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614208 | ||||||
| chr5:180614208
|
T | TGGTGGAT others(163): Show |
42 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(39): Show | 43 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.3220-30_3220-29ins others(170): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614208 | ||||||
| chr5:180614223
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-44G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614223 | ||||||
| chr5:180614240
|
CGTGGTGG others(27): Show |
C | 1 | a0001c0001t0027g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3220-95_3220-62del others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614240 | ||||||
| chr5:180614242
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(208): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.3220-63A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614242
|
T | TGGTGGAT others(27): Show |
1 | a0001c0001t0002g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3220-64_3220-63ins others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614242
|
T | TGGTGGAT others(27): Show |
20 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(17): Show | 20 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.3220-64_3220-63ins others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614242
|
T | TGGTGGAT others(197): Show |
1 | a0002c0002t0001g0347 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3220-64_3220-63ins others(204): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614242
|
T | TGGTGGAT others(231): Show |
2 | a0002c0004t0005g0278a0002c0004t0005g0285 | 2 | HG00438.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.3220-64_3220-63ins others(238): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614242
|
TGGTGGAT others(27): Show |
T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-97_3220-64del others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614242 | ||||||
| chr5:180614257
|
C | CGGAGGGA others(27): Show |
1 | a0005c0018t0011g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3220-79_3220-78ins others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614257 | ||||||
| chr5:180614274
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3220-95A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614274 | ||||||
| chr5:180614276
|
C | T | 1 | a0001c0009t0004g0013 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3220-97G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614276 | ||||||
| chr5:180614309
|
G | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-130C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614309 | ||||||
| chr5:180614310
|
T | C | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-131A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614310 | ||||||
| chr5:180614316
|
A | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0180a0001c0001t0001g0182others(9): Show | 13 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.3220-137T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614316 | ||||||
| chr5:180614491
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(109): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.3220-312G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614491 | ||||||
| chr5:180614530
|
T | C | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-351A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614530 | ||||||
| chr5:180614587
|
G | A | 1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3220-408C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614587 | ||||||
| chr5:180614637
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(335): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.3220-458C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614637 | ||||||
| chr5:180614662
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(206): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.3220-483C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614662 | ||||||
| chr5:180614686
|
C | G | 4 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.3220-507G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614686 | ||||||
| chr5:180614705
|
GC | G | 48 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(45): Show | 49 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3220-527delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614705 | ||||||
| chr5:180614725
|
A | AC | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0071others(2): Show | 5 | NA18951.hp2 NA18983.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.3220-547dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614725 | ||||||
| chr5:180614753
|
C | T | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3220-574G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614753 | ||||||
| chr5:180614808
|
C | T | 5 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3220-629G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614808 | ||||||
| chr5:180614868
|
C | A | 45 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(42): Show | 46 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.3220-689G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614868 | ||||||
| chr5:180614999
|
G | T | 337 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(334): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.3220-820C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180614999 | ||||||
| chr5:180615111
|
C | T | 1 | a0013c0019t0008g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3220-932G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615111 | ||||||
| chr5:180615121
|
A | G | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3220-942T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615121 | ||||||
| chr5:180615153
|
T | C | 52 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(49): Show | 53 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.3220-974A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615153 | ||||||
| chr5:180615180
|
CGGAGCAC others(38): Show |
C | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3220-1046_3220-100 others(49): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615180 | ||||||
| chr5:180615191
|
GC | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(205): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.3220-1013delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615191 | ||||||
| chr5:180615192
|
C | CCCCGCTG others(51): Show |
6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3220-1014_3220-101 others(62): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615192 | ||||||
| chr5:180615192
|
C | CCTGCCGG others(183): Show |
1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3220-1014_3220-101 others(194): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615192 | ||||||
| chr5:180615192
|
C | T | 3 | a0002c0002t0001g0211a0002c0002t0001g0349a0002c0002t0005g0340 | 3 | HG02683.hp1 HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3220-1013G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615192 | ||||||
| chr5:180615195
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(206): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.3220-1016G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615195 | ||||||
| chr5:180615198
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(229): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.3220-1019A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615198 | ||||||
| chr5:180615198
|
T | TGGTCAAC others(51): Show |
3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3220-1020_3220-101 others(62): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615198 | ||||||
| chr5:180615225
|
T | C | 102 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(99): Show | 104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.3220-1046A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615225 | ||||||
| chr5:180615238
|
C | A | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3220-1059G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615238 | ||||||
| chr5:180615243
|
T | C | 3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3220-1064A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615243 | ||||||
| chr5:180615249
|
A | C | 103 | a0001c0001t0001g0272a0001c0009t0001g0019a0001c0009t0001g0063others(100): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.3220-1070T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615249 | ||||||
| chr5:180615255
|
A | T | 103 | a0001c0001t0001g0272a0001c0009t0001g0019a0001c0009t0001g0063others(100): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.3220-1076T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615255 | ||||||
| chr5:180615257
|
CTCCACTT others(6): Show |
C | 46 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(43): Show | 47 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.3220-1091_3220-107 others(17): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615257 | ||||||
| chr5:180615292
|
G | GGGTCCCG others(37): Show |
42 | a0001c0023t0008g0377a0001c0023t0008g0378a0002c0002t0001g0002others(39): Show | 43 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.3219+1074_3219+107 others(48): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615292 | ||||||
| chr5:180615295
|
C | G | 42 | a0001c0023t0008g0377a0001c0023t0008g0378a0002c0002t0001g0002others(39): Show | 43 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.3219+1072G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615295 | ||||||
| chr5:180615295
|
C | T | 11 | a0001c0001t0001g0272a0001c0009t0001g0019a0001c0009t0001g0063others(8): Show | 11 | HG01175.hp2 HG01346.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+1072G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615295 | ||||||
| chr5:180615301
|
C | T | 61 | a0001c0001t0001g0272a0001c0009t0001g0019a0001c0009t0001g0063others(58): Show | 62 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.3219+1066G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615301 | ||||||
| chr5:180615336
|
T | TGGGCCCA others(345): Show |
1 | a0001c0001t0001g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3219+1030_3219+103 others(356): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615336 | ||||||
| chr5:180615340
|
C | CCCGCCGG others(37): Show |
10 | a0001c0009t0001g0019a0001c0009t0001g0063a0002c0002t0001g0016others(7): Show | 10 | HG01175.hp2 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.3219+1026_3219+102 others(48): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615340 | ||||||
| chr5:180615340
|
C | G | 42 | a0001c0023t0008g0377a0001c0023t0008g0378a0002c0002t0001g0002others(39): Show | 43 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.3219+1027G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615340 | ||||||
| chr5:180615346
|
T | C | 55 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(52): Show | 56 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.3219+1021A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615346 | ||||||
| chr5:180615360
|
CTCCACTT others(6): Show |
C | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+994_3219+1006 others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615360 | ||||||
| chr5:180615373
|
ATCCACTT others(185): Show |
A | 5 | a0001c0001t0002g0124a0001c0001t0002g0191a0001c0001t0002g0195others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3219+802_3219+993d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615373 | ||||||
| chr5:180615386
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3219+981G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615386 | ||||||
| chr5:180615395
|
G | GGGCCCGC others(302): Show |
1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3219+971_3219+972i others(311): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615395 | ||||||
| chr5:180615397
|
GT | G | 55 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(52): Show | 56 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.3219+969delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615397 | ||||||
| chr5:180615398
|
T | G | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3219+969A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615398 | ||||||
| chr5:180615404
|
T | C | 56 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(53): Show | 57 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.3219+963A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615404 | ||||||
| chr5:180615405
|
G | A | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+962C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615405 | ||||||
| chr5:180615418
|
C | CTCCACTT others(95): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3219+948_3219+949i others(104): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615418 | ||||||
| chr5:180615431
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0272 | 2 | HG04228.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3219+936G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615431 | ||||||
| chr5:180615439
|
T | TGGGCCCA others(38): Show |
47 | a0001c0001t0001g0092a0001c0001t0001g0360a0001c0001t0002g0055others(44): Show | 47 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.3219+927_3219+928i others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615439
|
T | TGGGCCCG others(38): Show |
49 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(46): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3219+927_3219+928i others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615439
|
T | TGGGCCCG others(1957): Show |
1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3219+927_3219+928i others(1966): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615439
|
T | TGGGCCCG others(171): Show |
2 | a0002c0002t0001g0339a0002c0002t0013g0165 | 2 | HG02083.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3219+927_3219+928i others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615439
|
T | TGGGCCCG others(304): Show |
4 | a0002c0002t0001g0016a0002c0002t0001g0351a0002c0002t0001g0353others(1): Show | 4 | HG00738.hp2 HG01070.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+927_3219+928i others(313): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615439
|
T | TGGGCCCG others(171): Show |
6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3219+927_3219+928i others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615439 | ||||||
| chr5:180615442
|
G | GC | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+924dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(494): Show |
2 | a0002c0003t0006g0334a0002c0003t0006g0335 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3219+924_3219+925i others(503): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(494): Show |
97 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(94): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.3219+924_3219+925i others(503): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(803): Show |
1 | a0007c0010t0015g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3219+924_3219+925i others(812): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(803): Show |
2 | a0007c0010t0010g0323a0007c0010t0015g0044 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3219+924_3219+925i others(812): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(391): Show |
1 | a0001c0001t0002g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3219+924_3219+925i others(400): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(984): Show |
1 | a0001c0001t0001g0365 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3219+924_3219+925i others(993): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(436): Show |
46 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(43): Show | 46 | HG00621.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.3219+924_3219+925i others(445): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(1363): Show |
1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3219+924_3219+925i others(1372): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(481): Show |
1 | a0001c0001t0016g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3219+924_3219+925i others(490): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCACCG others(377): Show |
1 | a0003c0005t0001g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3219+924_3219+925i others(386): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GCCCCGCT others(39): Show |
1 | a0001c0001t0001g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3219+924_3219+925i others(48): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615442
|
G | GGCCTGCC others(201): Show |
1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3219+924_3219+925i others(210): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615442 | ||||||
| chr5:180615445
|
C | CACCGGTC others(538): Show |
1 | a0001c0001t0001g0258 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3219+921_3219+922i others(547): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615445 | ||||||
| chr5:180615445
|
C | CACCGGTC others(229): Show |
2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3219+921_3219+922i others(238): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615445 | ||||||
| chr5:180615446
|
G | A | 12 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(9): Show | 12 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.3219+921C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615446 | ||||||
| chr5:180615448
|
C | T | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+919G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615448 | ||||||
| chr5:180615468
|
T | TTCCTTTT others(25): Show |
39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+898_3219+899i others(34): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615468 | ||||||
| chr5:180615470
|
CCGAAATC others(6): Show |
C | 12 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(9): Show | 12 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.3219+884_3219+896d others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615470 | ||||||
| chr5:180615472
|
G | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3219+895C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615472 | ||||||
| chr5:180615472
|
G | C | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+895C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615472 | ||||||
| chr5:180615473
|
A | T | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+894T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615473 | ||||||
| chr5:180615474
|
A | T | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+893T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615474 | ||||||
| chr5:180615475
|
A | C | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+892T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615475 | ||||||
| chr5:180615482
|
G | T | 159 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.3219+885C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615482 | ||||||
| chr5:180615483
|
T | C | 159 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.3219+884A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615483 | ||||||
| chr5:180615483
|
T | TCTTTCGG others(39): Show |
3 | a0001c0001t0001g0319a0002c0003t0006g0334a0002c0003t0006g0335 | 3 | HG01257.hp2 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3219+838_3219+883d others(48): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615483 | ||||||
| chr5:180615488
|
C | T | 39 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(36): Show | 40 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.3219+879G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615488 | ||||||
| chr5:180615496
|
TG | T | 16 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(13): Show | 16 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.3219+870delC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615496 | ||||||
| chr5:180615499
|
GGC | G | 143 | a0001c0001t0001g0092a0001c0001t0001g0360a0001c0001t0002g0055others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.3219+866_3219+867d others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615499 | ||||||
| chr5:180615500
|
G | T | 1 | a0019c0040t0002g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3219+867C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615500 | ||||||
| chr5:180615500
|
GC | G | 12 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(9): Show | 12 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.3219+866delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615500 | ||||||
| chr5:180615501
|
C | CCCCGCTG others(51): Show |
2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3219+865_3219+866i others(60): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615501 | ||||||
| chr5:180615501
|
C | T | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+866G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615501 | ||||||
| chr5:180615505
|
G | A | 13 | a0002c0002t0001g0016a0002c0002t0001g0061a0002c0002t0001g0339others(10): Show | 13 | HG00738.hp2 HG01070.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.3219+862C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615505 | ||||||
| chr5:180615507
|
C | T | 8 | a0002c0002t0001g0125a0002c0003t0001g0375a0002c0003t0010g0043others(5): Show | 8 | HG01175.hp2 HG01928.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3219+860G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615507 | ||||||
| chr5:180615527
|
TTCCTTTC others(24): Show |
T | 1 | a0001c0001t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3219+809_3219+839d others(33): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615527 | ||||||
| chr5:180615527
|
TTCCTTTC others(69): Show |
T | 11 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+764_3219+839d others(78): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615527 | ||||||
| chr5:180615534
|
C | T | 2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3219+833G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615534 | ||||||
| chr5:180615545
|
G | GGC | 88 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(85): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.3219+821_3219+822i others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615545 | ||||||
| chr5:180615548
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3219+819G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615548 | ||||||
| chr5:180615551
|
C | T | 2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3219+816G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615551 | ||||||
| chr5:180615551
|
CGGTCACC others(38): Show |
C | 2 | a0002c0003t0002g0325a0002c0003t0002g0336 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3219+771_3219+815d others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615551 | ||||||
| chr5:180615562
|
C | G | 1 | a0001c0001t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3219+805G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615562 | ||||||
| chr5:180615563
|
T | A | 1 | a0001c0001t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3219+804A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615563 | ||||||
| chr5:180615564
|
T | A | 1 | a0001c0001t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3219+803A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615564 | ||||||
| chr5:180615565
|
C | A | 1 | a0001c0001t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3219+802G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615565 | ||||||
| chr5:180615565
|
C | CTCCACTT others(140): Show |
1 | a0001c0001t0002g0372 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3219+801_3219+802i others(149): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615565 | ||||||
| chr5:180615578
|
C | T | 137 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.3219+789G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615578 | ||||||
| chr5:180615589
|
GT | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(168): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.3219+777delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615589 | ||||||
| chr5:180615590
|
T | C | 145 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3219+777A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615590 | ||||||
| chr5:180615590
|
T | G | 5 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(2): Show | 5 | HG01069.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3219+777A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615590 | ||||||
| chr5:180615593
|
C | T | 72 | a0001c0001t0001g0039a0001c0001t0001g0128a0001c0001t0001g0129others(69): Show | 73 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.3219+774G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615593 | ||||||
| chr5:180615594
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3219+773C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615594 | ||||||
| chr5:180615596
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.3219+771A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615596 | ||||||
| chr5:180615596
|
T | TGGTCACC others(170): Show |
9 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(6): Show | 9 | HG00423.hp2 HG00558.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.3219+770_3219+771i others(179): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615596 | ||||||
| chr5:180615596
|
T | TGGTCACC others(304): Show |
1 | a0001c0032t0026g0333 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3219+770_3219+771i others(313): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615596 | ||||||
| chr5:180615607
|
C | G | 11 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+760G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615607 | ||||||
| chr5:180615608
|
T | A | 11 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+759A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615608 | ||||||
| chr5:180615609
|
T | A | 11 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+758A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615609 | ||||||
| chr5:180615610
|
C | A | 11 | a0001c0001t0001g0075a0001c0001t0002g0066a0001c0001t0002g0067others(8): Show | 11 | HG00741.hp2 HG01256.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.3219+757G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615610 | ||||||
| chr5:180615610
|
C | CTCCACTT others(6): Show |
1 | a0003c0005t0001g0036 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3219+756_3219+757i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615610 | ||||||
| chr5:180615613
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3219+754G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615613 | ||||||
| chr5:180615618
|
C | CCGAAATC others(6): Show |
4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+748_3219+749i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615618 | ||||||
| chr5:180615623
|
C | T | 130 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.3219+744G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615623 | ||||||
| chr5:180615625
|
G | A | 17 | a0001c0001t0002g0055a0001c0001t0002g0177a0001c0001t0002g0216others(14): Show | 17 | HG01099.hp2 HG01975.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.3219+742C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615625 | ||||||
| chr5:180615634
|
G | GGC | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+732_3219+733i others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615634 | ||||||
| chr5:180615634
|
G | GGCCTGCC others(156): Show |
37 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(34): Show | 37 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.3219+732_3219+733i others(165): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615634 | ||||||
| chr5:180615637
|
C | T | 88 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(85): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.3219+730G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615637 | ||||||
| chr5:180615638
|
G | A | 6 | a0001c0001t0002g0124a0001c0001t0002g0191a0001c0001t0002g0195others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3219+729C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615638 | ||||||
| chr5:180615640
|
C | T | 38 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(35): Show | 38 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.3219+727G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615640 | ||||||
| chr5:180615675
|
T | TG | 15 | a0001c0001t0002g0124a0001c0001t0002g0191a0001c0001t0002g0195others(12): Show | 15 | HG00423.hp2 HG00558.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3219+691dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615675 | ||||||
| chr5:180615675
|
T | TGGGCCCG others(38): Show |
1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3219+691_3219+692i others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615675 | ||||||
| chr5:180615675
|
T | TGGGCCCG others(171): Show |
1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3219+691_3219+692i others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615675 | ||||||
| chr5:180615678
|
G | GC | 41 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071others(38): Show | 41 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.3219+688dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615678 | ||||||
| chr5:180615681
|
T | C | 236 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.3219+686A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615681 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(627): Show |
1 | a0002c0002t0001g0345 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3219+670_3219+671i others(636): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(583): Show |
34 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0023t0008g0377others(31): Show | 35 | HG00609.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.3219+670_3219+671i others(592): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(583): Show |
2 | a0002c0002t0001g0352a0002c0002t0001g0355 | 2 | HG01071.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.3219+670_3219+671i others(592): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(716): Show |
1 | a0002c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3219+670_3219+671i others(725): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(717): Show |
1 | a0002c0008t0004g0296 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3219+670_3219+671i others(726): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(716): Show |
33 | a0001c0009t0004g0013a0001c0009t0014g0083a0002c0002t0001g0027others(30): Show | 34 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.3219+670_3219+671i others(725): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(304): Show |
2 | a0002c0002t0001g0016a0002c0002t0001g0339 | 2 | HG02083.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3219+670_3219+671i others(313): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(466): Show |
1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3219+670_3219+671i others(475): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(304): Show |
3 | a0002c0002t0001g0351a0002c0002t0001g0353a0002c0002t0001g0354 | 3 | HG00738.hp2 HG01070.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3219+670_3219+671i others(313): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(420): Show |
6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3219+670_3219+671i others(429): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615696
|
T | TTCTCCAC others(303): Show |
1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3219+670_3219+671i others(312): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615696 | ||||||
| chr5:180615698
|
CTCCACTT others(6): Show |
C | 99 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0075others(96): Show | 102 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.3219+656_3219+668d others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615698 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(24): Show |
6 | a0001c0001t0001g0168a0001c0001t0001g0198a0001c0001t0006g0209others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.3219+662_3219+663i others(33): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(68): Show |
3 | a0001c0001t0001g0113a0001c0001t0006g0188a0007c0010t0015g0252 | 3 | HG01981.hp2 HG03225.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3219+662_3219+663i others(77): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(480): Show |
1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3219+662_3219+663i others(489): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(24): Show |
80 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(77): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3219+662_3219+663i others(33): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(471): Show |
1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3219+662_3219+663i others(480): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(68): Show |
1 | a0001c0001t0002g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3219+662_3219+663i others(77): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTC others(82): Show |
1 | a0002c0002t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3219+662_3219+663i others(91): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTT others(69): Show |
1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+662_3219+663i others(78): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615704
|
T | TTCCTTTT others(568): Show |
1 | a0003c0005t0001g0036 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3219+662_3219+663i others(577): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615704 | ||||||
| chr5:180615708
|
G | C | 96 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(93): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3219+659C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615708 | ||||||
| chr5:180615709
|
A | T | 95 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3219+658T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615709 | ||||||
| chr5:180615710
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3219+657T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615710 | ||||||
| chr5:180615710
|
A | T | 95 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3219+657T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615710 | ||||||
| chr5:180615711
|
A | AGCACTGG others(21): Show |
1 | a0001c0001t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3219+655_3219+656i others(30): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
A | ATCCACTG others(127): Show |
1 | a0022c0045t0005g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3219+655_3219+656i others(136): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
A | ATCCACTG others(127): Show |
3 | a0001c0001t0001g0360a0001c0001t0008g0144a0005c0018t0013g0167 | 3 | HG01261.hp1 HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3219+655_3219+656i others(136): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
A | ATCCACTG others(129): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0071 | 3 | HG01168.hp2 HG01169.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.3219+655_3219+656i others(138): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
A | ATCCACTG others(127): Show |
1 | a0003c0005t0002g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3219+655_3219+656i others(136): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
A | C | 95 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3219+656T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615711
|
ATCCACTT others(37): Show |
A | 21 | a0002c0003t0003g0028a0002c0003t0003g0073a0002c0003t0003g0074others(18): Show | 21 | HG00597.hp1 HG00673.hp2 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.3219+612_3219+655d others(46): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615711 | ||||||
| chr5:180615718
|
T | G | 32 | a0001c0001t0001g0092a0001c0001t0001g0180a0001c0001t0001g0182others(29): Show | 32 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.3219+649A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615718 | ||||||
| chr5:180615719
|
C | T | 32 | a0001c0001t0001g0092a0001c0001t0001g0180a0001c0001t0001g0182others(29): Show | 32 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.3219+648G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615719 | ||||||
| chr5:180615724
|
C | T | 3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3219+643G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615724 | ||||||
| chr5:180615732
|
T | TG | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+634dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615732 | ||||||
| chr5:180615735
|
G | GC | 86 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(83): Show | 88 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.3219+631dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615735 | ||||||
| chr5:180615735
|
G | GGC | 32 | a0001c0001t0001g0092a0001c0001t0001g0180a0001c0001t0001g0182others(29): Show | 32 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.3219+631_3219+632i others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615735 | ||||||
| chr5:180615738
|
C | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0002g0290others(8): Show | 11 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3219+629G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615738 | ||||||
| chr5:180615739
|
G | A | 11 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0115others(8): Show | 11 | HG00423.hp2 HG00558.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.3219+628C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615739 | ||||||
| chr5:180615755
|
C | CTCCACTT others(6): Show |
4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+611_3219+612i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615755 | ||||||
| chr5:180615768
|
C | T | 2 | a0002c0002t0001g0115a0002c0002t0001g0251 | 2 | HG03669.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.3219+599G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615768 | ||||||
| chr5:180615776
|
T | TG | 4 | a0002c0003t0001g0321a0002c0003t0001g0370a0002c0003t0006g0334others(1): Show | 4 | HG02486.hp2 HG02647.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+590dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615776 | ||||||
| chr5:180615779
|
GC | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.3219+587delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615779 | ||||||
| chr5:180615780
|
C | CCCGCCGG others(746): Show |
1 | a0001c0001t0002g0372 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3219+586_3219+587i others(755): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615780 | ||||||
| chr5:180615780
|
C | G | 1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+587G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615780 | ||||||
| chr5:180615780
|
C | T | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3219+587G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615780 | ||||||
| chr5:180615783
|
C | CGCCGGTC others(37): Show |
1 | a0011c0016t0011g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3219+540_3219+583d others(46): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615783 | ||||||
| chr5:180615783
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(192): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.3219+584G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615783 | ||||||
| chr5:180615786
|
C | T | 88 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(85): Show | 90 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.3219+581G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615786 | ||||||
| chr5:180615794
|
T | C | 1 | a0002c0003t0003g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3219+573A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615794 | ||||||
| chr5:180615800
|
C | CTCCACTT others(6): Show |
1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+566_3219+567i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615800 | ||||||
| chr5:180615813
|
C | T | 15 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0115others(12): Show | 15 | HG00423.hp2 HG00558.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.3219+554G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615813 | ||||||
| chr5:180615824
|
G | GC | 10 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(7): Show | 10 | HG00423.hp2 HG00558.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3219+542dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615824 | ||||||
| chr5:180615824
|
G | GCCCCGCT others(52): Show |
1 | a0002c0002t0004g0187 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3219+542_3219+543i others(61): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615824 | ||||||
| chr5:180615824
|
G | GCCCCGCT others(52): Show |
84 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3219+542_3219+543i others(61): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615824 | ||||||
| chr5:180615827
|
T | C | 124 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0001g0225others(121): Show | 126 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.3219+540A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615827 | ||||||
| chr5:180615828
|
G | A | 1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+539C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615828 | ||||||
| chr5:180615830
|
C | T | 95 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(92): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3219+537G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615830 | ||||||
| chr5:180615857
|
C | T | 13 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(10): Show | 13 | HG00423.hp2 HG00558.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.3219+510G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615857 | ||||||
| chr5:180615858
|
G | A | 1 | a0022c0045t0005g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3219+509C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615858 | ||||||
| chr5:180615868
|
G | GC | 4 | a0002c0004t0031g0279a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02723.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+498dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615868 | ||||||
| chr5:180615871
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(322): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.3219+496A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615871 | ||||||
| chr5:180615871
|
TGCCGGTC others(38): Show |
T | 1 | a0002c0003t0002g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3219+451_3219+495d others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615871 | ||||||
| chr5:180615887
|
T | A | 4 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(1): Show | 4 | HG02647.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+480A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615887 | ||||||
| chr5:180615901
|
C | T | 3 | a0002c0002t0001g0115a0002c0002t0001g0251a0002c0002t0004g0056 | 3 | HG02738.hp2 HG03669.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.3219+466G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615901 | ||||||
| chr5:180615912
|
GC | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.3219+454delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615912 | ||||||
| chr5:180615915
|
C | T | 4 | a0002c0003t0002g0325a0002c0003t0002g0336a0002c0003t0003g0289others(1): Show | 4 | HG01891.hp2 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+452G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615915 | ||||||
| chr5:180615916
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(190): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.3219+451G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615916 | ||||||
| chr5:180615919
|
C | T | 96 | a0001c0001t0002g0124a0001c0001t0002g0191a0001c0001t0002g0195others(93): Show | 98 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.3219+448G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615919 | ||||||
| chr5:180615933
|
C | CTCCACTT others(6): Show |
85 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(82): Show | 87 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.3219+433_3219+434i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615933 | ||||||
| chr5:180615933
|
C | CTCCACTT others(567): Show |
1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3219+433_3219+434i others(576): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615933 | ||||||
| chr5:180615933
|
C | CTCCACTT others(567): Show |
1 | a0002c0002t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3219+433_3219+434i others(576): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615933 | ||||||
| chr5:180615946
|
C | T | 11 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(8): Show | 11 | HG00423.hp2 HG00558.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.3219+421G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615946 | ||||||
| chr5:180615947
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3219+420C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615947 | ||||||
| chr5:180615957
|
GC | G | 47 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(44): Show | 47 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.3219+409delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615957 | ||||||
| chr5:180615958
|
C | T | 87 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(84): Show | 89 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3219+409G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615958 | ||||||
| chr5:180615961
|
C | T | 5 | a0001c0001t0012g0223a0002c0003t0001g0321a0002c0003t0001g0370others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.3219+406G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615961 | ||||||
| chr5:180615964
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(285): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.3219+403G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615964 | ||||||
| chr5:180615965
|
G | A | 3 | a0002c0003t0010g0043a0002c0003t0010g0178a0029c0028t0010g0179 | 3 | HG02647.hp1 HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3219+402C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615965 | ||||||
| chr5:180615966
|
G | GT | 3 | a0001c0001t0001g0121a0001c0006t0001g0154a0001c0006t0001g0157 | 3 | HG01109.hp2 HG01346.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3219+400dupA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615966 | ||||||
| chr5:180615991
|
C | T | 12 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3219+376G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615991 | ||||||
| chr5:180615999
|
T | TG | 10 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(7): Show | 10 | HG00423.hp2 HG00558.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3219+367dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180615999 | ||||||
| chr5:180616005
|
T | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3219+362A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616005 | ||||||
| chr5:180616008
|
C | CGGTCACC others(420): Show |
1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3219+358_3219+359i others(429): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616008 | ||||||
| chr5:180616008
|
C | CGGTCACC others(567): Show |
9 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(6): Show | 9 | HG00423.hp2 HG00558.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.3219+358_3219+359i others(576): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616008 | ||||||
| chr5:180616008
|
C | CGGTCACC others(38): Show |
1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3219+358_3219+359i others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616008 | ||||||
| chr5:180616035
|
C | T | 1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+332G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616035 | ||||||
| chr5:180616046
|
G | GC | 91 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(88): Show | 93 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.3219+320dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616046 | ||||||
| chr5:180616047
|
CCTGCCGG others(36): Show |
C | 5 | a0001c0001t0002g0124a0001c0001t0002g0191a0001c0001t0002g0195others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3219+277_3219+319d others(45): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616047 | ||||||
| chr5:180616049
|
T | C | 127 | a0001c0001t0002g0290a0001c0001t0005g0117a0001c0001t0012g0223others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.3219+318A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616049 | ||||||
| chr5:180616050
|
G | C | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3219+317C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616050 | ||||||
| chr5:180616051
|
C | G | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3219+316G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616051 | ||||||
| chr5:180616052
|
C | T | 2 | a0002c0002t0004g0056a0007c0010t0015g0252 | 2 | HG02738.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3219+315G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616052 | ||||||
| chr5:180616074
|
C | CCGAAATC others(6): Show |
87 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(84): Show | 89 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3219+292_3219+293i others(15): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616074 | ||||||
| chr5:180616079
|
C | T | 1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+288G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616079 | ||||||
| chr5:180616090
|
G | GC | 194 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(191): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.3219+276dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GCCCCGCC others(53): Show |
8 | a0001c0009t0002g0114a0002c0002t0001g0072a0002c0002t0001g0120others(5): Show | 8 | HG00423.hp2 HG00558.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.3219+276_3219+277i others(62): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GCCCCGCC others(54): Show |
1 | a0002c0002t0018g0109 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3219+276_3219+277i others(63): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GCCCCGCT others(156): Show |
1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3219+276_3219+277i others(165): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GCCCCGCT others(127): Show |
1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3219+276_3219+277i others(136): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GGC | 87 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0004g0013others(84): Show | 89 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3219+276_3219+277i others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616090
|
G | GGCCTGCC others(480): Show |
1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3219+276_3219+277i others(489): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616090 | ||||||
| chr5:180616093
|
T | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(307): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.3219+274A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616093 | ||||||
| chr5:180616096
|
C | CGGTCACC others(171): Show |
1 | a0001c0001t0012g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3219+270_3219+271i others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(171): Show |
19 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(16): Show | 19 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.3219+270_3219+271i others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(126): Show |
4 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.3219+270_3219+271i others(135): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(259): Show |
2 | a0002c0003t0006g0334a0002c0003t0006g0335 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3219+270_3219+271i others(268): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(215): Show |
1 | a0002c0003t0001g0321 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3219+270_3219+271i others(224): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(258): Show |
1 | a0001c0001t0002g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3219+270_3219+271i others(267): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | CGGTCACC others(82): Show |
4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3219+270_3219+271i others(91): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616096
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(197): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.3219+271G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616096 | ||||||
| chr5:180616330
|
C | G | 22 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.3219+37G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616330 | ||||||
| chr5:180616330
|
C | T | 1 | a0002c0003t0007g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3219+37G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 23/29 | chr5 | 180616330 | ||||||
| chr5:180616689
|
G | A | 1 | a0002c0003t0003g0132 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3097-200C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 22/29 | chr5 | 180616689 | ||||||
| chr5:180616717
|
G | A | 1 | a0007c0010t0010g0323 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3096+183C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 22/29 | chr5 | 180616717 | ||||||
| chr5:180616731
|
C | A | 97 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(94): Show | 99 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.3096+169G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 22/29 | chr5 | 180616731 | ||||||
| chr5:180617012
|
G | T | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3002-18C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617012 | ||||||
| chr5:180617017
|
C | A | 1 | a0003c0005t0002g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3002-23G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617017 | ||||||
| chr5:180617095
|
C | T | 1 | a0006c0014t0009g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3002-101G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617095 | ||||||
| chr5:180617103
|
A | C | 3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3002-109T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617103 | ||||||
| chr5:180617119
|
ATCCTACT others(243): Show |
A | 5 | a0002c0003t0001g0370a0002c0003t0001g0375a0002c0003t0010g0178others(2): Show | 5 | HG02647.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3002-375_3002-126d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617119 | ||||||
| chr5:180617121
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3002-127G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617121 | ||||||
| chr5:180617169
|
ATCCTACT others(193): Show |
A | 2 | a0002c0012t0001g0052a0002c0012t0021g0174 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3002-375_3002-176d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617169 | ||||||
| chr5:180617169
|
ATCCTACT others(293): Show |
A | 3 | a0001c0001t0027g0231a0002c0003t0019g0186a0002c0003t0019g0250 | 3 | HG02630.hp2 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3002-475_3002-176d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617169 | ||||||
| chr5:180617203
|
CCTCTGGG others(143): Show |
C | 6 | a0001c0047t0001g0173a0002c0002t0013g0165a0005c0015t0011g0171others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3002-359_3002-210d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617203 | ||||||
| chr5:180617219
|
G | A | 93 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(90): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.3002-225C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617219 | ||||||
| chr5:180617253
|
CCTCTGGG others(93): Show |
C | 4 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(1): Show | 4 | HG02074.hp1 HG02135.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002-359_3002-260d others(102): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617253 | ||||||
| chr5:180617265
|
A | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(315): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3002-271T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617265 | ||||||
| chr5:180617269
|
G | A | 7 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(4): Show | 7 | HG01167.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3002-275C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617269 | ||||||
| chr5:180617297
|
C | T | 2 | a0001c0001t0001g0309a0005c0018t0011g0041 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3002-303G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617297 | ||||||
| chr5:180617303
|
A | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(315): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3002-309T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617303 | ||||||
| chr5:180617353
|
A | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(315): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3002-359T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617353 | ||||||
| chr5:180617359
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3002-365C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617359 | ||||||
| chr5:180617369
|
GTCCTACT others(43): Show |
G | 1 | a0002c0003t0007g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3002-425_3002-376d others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617369 | ||||||
| chr5:180617375
|
C | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(271): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.3002-381G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617375 | ||||||
| chr5:180617381
|
A | G | 1 | a0006c0033t0009g0376 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3002-387T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617381 | ||||||
| chr5:180617391
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3002-397G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617391 | ||||||
| chr5:180617410
|
G | T | 2 | a0014c0020t0007g0170a0014c0020t0013g0271 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3002-416C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617410 | ||||||
| chr5:180617419
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(250): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.3002-425T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617419 | ||||||
| chr5:180617426
|
TCCAGAGC others(646): Show |
T | 2 | a0001c0001t0001g0259a0009c0024t0001g0004 | 3 | HG00140.hp1 HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.3001+691_3002-433d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617426 | ||||||
| chr5:180617453
|
C | T | 2 | a0002c0012t0001g0052a0002c0012t0021g0174 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3002-459G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617453 | ||||||
| chr5:180617460
|
G | T | 3 | a0001c0001t0001g0365a0014c0020t0007g0170a0014c0020t0013g0271 | 3 | HG02572.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3002-466C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617460 | ||||||
| chr5:180617469
|
G | A | 93 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(90): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.3002-475C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617469 | ||||||
| chr5:180617475
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3002-481G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617475 | ||||||
| chr5:180617483
|
CACCCTCT others(948): Show |
C | 91 | a0001c0009t0001g0019a0001c0009t0001g0063a0001c0009t0002g0114others(88): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.3001+332_3002-490d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617483 | ||||||
| chr5:180617503
|
C | T | 2 | a0002c0003t0001g0370a0002c0012t0023g0045 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3002-509G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617503 | ||||||
| chr5:180617510
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(220): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.3002-516C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617510 | ||||||
| chr5:180617519
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(221): Show | 228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.3002-525C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617519 | ||||||
| chr5:180617519
|
GTCCTACT others(646): Show |
G | 1 | a0002c0003t0010g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3001+598_3002-526d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617519 | ||||||
| chr5:180617525
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(226): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.3002-531G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617525 | ||||||
| chr5:180617560
|
G | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(1): Show | 4 | HG02074.hp1 HG02135.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002-566C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617560 | ||||||
| chr5:180617569
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(1): Show | 4 | HG02074.hp1 HG02135.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002-575C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617569 | ||||||
| chr5:180617575
|
C | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(2): Show | 5 | HG02074.hp1 HG02135.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3002-581G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617575 | ||||||
| chr5:180617575
|
CTCCAGAG others(43): Show |
C | 1 | a0002c0003t0003g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3002-631_3002-582d others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617575 | ||||||
| chr5:180617576
|
T | TC | 222 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.3002-583dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617576 | ||||||
| chr5:180617576
|
T | TCCCAGAG others(95): Show |
1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3002-583_3002-582i others(104): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617576 | ||||||
| chr5:180617577
|
CCAGAGCA others(42): Show |
C | 1 | a0001c0001t0001g0330 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3002-632_3002-584d others(51): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617577 | ||||||
| chr5:180617602
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.3002-608C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617602 | ||||||
| chr5:180617610
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3002-616C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617610 | ||||||
| chr5:180617610
|
GACACCCA others(143): Show |
G | 1 | a0002c0003t0007g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3002-766_3002-617d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617610 | ||||||
| chr5:180617619
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3002-625C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617619 | ||||||
| chr5:180617624
|
A | AC | 4 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(1): Show | 4 | HG02074.hp1 HG02135.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002-631_3002-630i others(3): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617624 | ||||||
| chr5:180617625
|
T | C | 9 | a0001c0001t0027g0231a0001c0047t0001g0173a0002c0002t0013g0165others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3002-631A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617625 | ||||||
| chr5:180617626
|
T | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0366others(1): Show | 4 | HG02074.hp1 HG02135.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002-632A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617626 | ||||||
| chr5:180617647
|
C | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(214): Show | 220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.3002-653G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617647 | ||||||
| chr5:180617652
|
G | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0330others(2): Show | 5 | HG02074.hp1 HG02135.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3002-658C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617652 | ||||||
| chr5:180617660
|
G | T | 6 | a0001c0047t0001g0173a0002c0002t0013g0165a0005c0015t0011g0171others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3002-666C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617660 | ||||||
| chr5:180617668
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.3002-674G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617668 | ||||||
| chr5:180617675
|
C | CTCCCAGA others(44): Show |
1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3002-682_3002-681i others(53): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617675 | ||||||
| chr5:180617675
|
C | T | 14 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0330others(11): Show | 14 | HG02074.hp1 HG02135.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3002-681G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617675 | ||||||
| chr5:180617677
|
CCAGAGCA others(42): Show |
C | 222 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.3002-732_3002-684d others(51): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617677 | ||||||
| chr5:180617697
|
C | A | 9 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0319others(6): Show | 9 | HG01257.hp2 HG02074.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.3002-703G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617697 | ||||||
| chr5:180617718
|
C | T | 8 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0319others(5): Show | 8 | HG01257.hp2 HG02074.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3002-724G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617718 | ||||||
| chr5:180617726
|
T | TC | 15 | a0001c0001t0001g0169a0001c0001t0001g0261a0001c0001t0001g0319others(12): Show | 15 | HG01257.hp2 HG02074.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.3002-733dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617726 | ||||||
| chr5:180617752
|
G | A | 6 | a0001c0047t0001g0173a0002c0002t0013g0165a0005c0015t0011g0171others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3002-758C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617752 | ||||||
| chr5:180617760
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(228): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.3002-766A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617760 | ||||||
| chr5:180617760
|
T | G | 10 | a0001c0047t0001g0173a0002c0002t0013g0165a0002c0003t0001g0370others(7): Show | 10 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.3002-766A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617760 | ||||||
| chr5:180617769
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(231): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.3002-775C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617769 | ||||||
| chr5:180617769
|
GTCCTATT others(396): Show |
G | 3 | a0002c0003t0001g0375a0002c0003t0010g0178a0029c0028t0010g0179 | 3 | HG02647.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3001+598_3002-776d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617769 | ||||||
| chr5:180617797
|
C | A | 6 | a0001c0047t0001g0173a0002c0002t0013g0165a0005c0015t0011g0171others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3002-803G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617797 | ||||||
| chr5:180617818
|
C | T | 6 | a0001c0047t0001g0173a0002c0002t0013g0165a0005c0015t0011g0171others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3002-824G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617818 | ||||||
| chr5:180617827
|
C | T | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3002-833G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617827 | ||||||
| chr5:180617853
|
A | G | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3002-859T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617853 | ||||||
| chr5:180617861
|
G | A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3002-867C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617861 | ||||||
| chr5:180617861
|
G | GACACCCA others(93): Show |
1 | a0002c0003t0007g0314 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3002-868_3002-867i others(102): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617861 | ||||||
| chr5:180617870
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.3002-876C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617870 | ||||||
| chr5:180617888
|
C | T | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3001+882G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617888 | ||||||
| chr5:180617891
|
T | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(227): Show | 234 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.3001+879A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617891 | ||||||
| chr5:180617898
|
A | C | 1 | a0002c0003t0007g0314 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3001+872T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617898 | ||||||
| chr5:180617919
|
C | T | 3 | a0002c0012t0001g0052a0002c0012t0021g0174a0002c0012t0023g0045 | 3 | HG02723.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+851G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617919 | ||||||
| chr5:180617925
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3001+845T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617925 | ||||||
| chr5:180617928
|
CCCAGAGC others(194): Show |
C | 3 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174 | 3 | HG02647.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+641_3001+841d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617928 | ||||||
| chr5:180617954
|
G | A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3001+816C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617954 | ||||||
| chr5:180617962
|
G | A | 1 | a0002c0012t0023g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3001+808C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617962 | ||||||
| chr5:180617977
|
TTCCAGAG others(43): Show |
T | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3001+743_3001+792d others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617977 | ||||||
| chr5:180617985
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(234): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.3001+785A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617985 | ||||||
| chr5:180617999
|
A | C | 7 | a0002c0012t0023g0045a0006c0014t0002g0374a0006c0014t0009g0301others(4): Show | 7 | HG01167.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3001+771T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180617999 | ||||||
| chr5:180618021
|
A | G | 2 | a0002c0012t0023g0045a0020c0044t0005g0281 | 2 | HG02723.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3001+749T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618021 | ||||||
| chr5:180618029
|
CCAGAGCA others(143): Show |
C | 1 | a0002c0012t0023g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3001+591_3001+740d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618029 | ||||||
| chr5:180618049
|
C | A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3001+721G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618049 | ||||||
| chr5:180618077
|
CTCCCAGA others(44): Show |
C | 1 | a0005c0015t0011g0288 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3001+642_3001+692d others(53): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618077 | ||||||
| chr5:180618163
|
G | A | 3 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174 | 3 | HG02647.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+607C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618163 | ||||||
| chr5:180618172
|
A | ATCCTATT others(195): Show |
1 | a0001c0001t0003g0338 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3001+597_3001+598i others(204): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618172 | ||||||
| chr5:180618178
|
T | TTCCAGAG others(94): Show |
1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3001+491_3001+591d others(103): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618178 | ||||||
| chr5:180618200
|
C | A | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3001+570G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618200 | ||||||
| chr5:180618236
|
G | A | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3001+534C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618236 | ||||||
| chr5:180618273
|
G | A | 1 | a0002c0012t0023g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3001+497C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618273 | ||||||
| chr5:180618280
|
T | TC | 3 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174 | 3 | HG02647.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+489dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618280 | ||||||
| chr5:180618300
|
CCCTCAGC others(94): Show |
C | 2 | a0002c0004t0003g0161a0002c0004t0005g0145 | 2 | HG00544.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3001+369_3001+469d others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618300 | ||||||
| chr5:180618323
|
G | A | 3 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174 | 3 | HG02647.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+447C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618323 | ||||||
| chr5:180618323
|
GTCCTACT others(44): Show |
G | 1 | a0002c0012t0023g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3001+396_3001+446d others(53): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618323 | ||||||
| chr5:180618330
|
TC | T | 3 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174 | 3 | HG02647.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3001+439delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618330 | ||||||
| chr5:180618331
|
C | CCCAGAGC others(43): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02970.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3001+438_3001+439i others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618331 | ||||||
| chr5:180618361
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG03017.hp2 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3001+409G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618361 | ||||||
| chr5:180618374
|
A | G | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG00323.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3001+396T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618374 | ||||||
| chr5:180618376
|
C | T | 6 | a0006c0014t0002g0374a0006c0014t0009g0301a0006c0014t0009g0302others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3001+394G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618376 | ||||||
| chr5:180618388
|
C | G | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3001+382G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618388 | ||||||
| chr5:180618401
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(242): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.3001+369A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618401 | ||||||
| chr5:180618438
|
G | C | 4 | a0002c0003t0001g0370a0002c0012t0001g0052a0002c0012t0021g0174others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3001+332C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618438 | ||||||
| chr5:180618453
|
C | T | 22 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.3001+317G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618453 | ||||||
| chr5:180618491
|
G | C | 2 | a0006c0033t0009g0376a0024c0046t0009g0327 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3001+279C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618491 | ||||||
| chr5:180618604
|
C | T | 22 | a0001c0001t0005g0117a0002c0003t0005g0103a0002c0003t0005g0318others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.3001+166G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618604 | ||||||
| chr5:180618686
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3001+84C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618686 | ||||||
| chr5:180618700
|
G | GGGTTACC others(3): Show |
241 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.3001+69_3001+70ins others(10): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 21/29 | chr5 | 180618700 | ||||||
| chr5:180618981
|
T | TC | 7 | a0001c0001t0001g0121a0002c0002t0001g0256a0002c0003t0002g0237others(4): Show | 7 | HG00621.hp2 HG02738.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2850+39dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 20/29 | chr5 | 180618981 | ||||||
| chr5:180619209
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(229): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2761+44G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 19/29 | chr5 | 180619209 | ||||||
| chr5:180619233
|
G | C | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2761+20C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 19/29 | chr5 | 180619233 | ||||||
| chr5:180619372
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01934.hp1 | splice_region_variant&intron_variant | LOW | c.2648-6C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619372 | ||||||
| chr5:180619426
|
C | CTGGCCGC others(15): Show |
233 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(230): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.2648-61_2648-60ins others(22): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619426 | ||||||
| chr5:180619492
|
CAG | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(241): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.2648-128_2648-127d others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619492 | ||||||
| chr5:180619495
|
A | C | 1 | a0022c0045t0005g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2648-129T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619495 | ||||||
| chr5:180619597
|
C | T | 1 | a0002c0002t0003g0248 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2647+68G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619597 | ||||||
| chr5:180619636
|
G | C | 5 | a0001c0001t0001g0092a0001c0001t0006g0051a0001c0001t0016g0023others(2): Show | 5 | HG00597.hp2 HG02132.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.2647+29C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 18/29 | chr5 | 180619636 | ||||||
| chr5:180619839
|
G | A | 42 | a0001c0009t0001g0019a0002c0002t0001g0002a0002c0002t0001g0011others(39): Show | 43 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2543-70C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/29 | chr5 | 180619839 | ||||||
| chr5:180619885
|
G | A | 46 | a0001c0009t0002g0114a0001c0009t0004g0013a0001c0009t0014g0083others(43): Show | 47 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.2543-116C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/29 | chr5 | 180619885 | ||||||
| chr5:180619913
|
G | A | 2 | a0002c0003t0003g0134a0002c0003t0003g0141 | 2 | NA18944.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2543-144C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/29 | chr5 | 180619913 | ||||||
| chr5:180619932
|
G | T | 1 | a0001c0001t0003g0050 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2543-163C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/29 | chr5 | 180619932 | ||||||
| chr5:180619934
|
G | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0024others(203): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2543-165C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 17/29 | chr5 | 180619934 | ||||||
| chr5:180620412
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(291): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.2407-104A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 16/29 | chr5 | 180620412 | ||||||
| chr5:180620739
|
C | CGT | 13 | a0001c0023t0008g0377a0001c0023t0008g0378a0002c0002t0001g0027others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2300-26_2300-25dup others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/29 | chr5 | 180620739 | ||||||
| chr5:180620739
|
C | CGTGT | 43 | a0001c0009t0001g0019a0002c0002t0001g0002a0002c0002t0001g0011others(40): Show | 44 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2300-28_2300-25dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/29 | chr5 | 180620739 | ||||||
| chr5:180620793
|
G | C | 44 | a0001c0009t0001g0019a0002c0002t0001g0002a0002c0002t0001g0011others(41): Show | 45 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.2300-78C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/29 | chr5 | 180620793 | ||||||
| chr5:180620863
|
C | G | 365 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(362): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2299+13G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 15/29 | chr5 | 180620863 | ||||||
| chr5:180621035
|
T | C | 45 | a0001c0001t0001g0106a0001c0009t0002g0114a0001c0009t0004g0013others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2168-28A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 14/29 | chr5 | 180621035 | ||||||
| chr5:180621056
|
C | T | 97 | a0001c0009t0001g0019a0001c0009t0002g0114a0001c0009t0004g0013others(94): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2168-49G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 14/29 | chr5 | 180621056 | ||||||
| chr5:180621316
|
C | G | 29 | a0001c0001t0001g0092a0001c0001t0001g0128a0001c0001t0001g0129others(26): Show | 29 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2021-64G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 13/29 | chr5 | 180621316 | ||||||
| chr5:180621361
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0365 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2021-109C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 13/29 | chr5 | 180621361 | ||||||
| chr5:180621474
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2020+68C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 13/29 | chr5 | 180621474 | ||||||
| chr5:180621972
|
C | A | 23 | a0001c0001t0012g0005a0001c0001t0012g0223a0001c0001t0012g0357others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.1658-68G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180621972 | ||||||
| chr5:180621986
|
G | GCCTC | 297 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(294): Show | 304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1658-86_1658-83dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180621986 | ||||||
| chr5:180622152
|
C | T | 35 | a0001c0001t0001g0220a0001c0001t0001g0309a0001c0001t0002g0307others(32): Show | 35 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1658-248G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622152 | ||||||
| chr5:180622172
|
A | G | 1 | a0001c0001t0010g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1658-268T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622172 | ||||||
| chr5:180622178
|
G | C | 38 | a0001c0001t0001g0299a0001c0001t0001g0356a0001c0001t0002g0047others(35): Show | 38 | HG00642.hp1 HG01109.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1658-274C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622178 | ||||||
| chr5:180622181
|
C | T | 45 | a0001c0001t0001g0092a0001c0001t0001g0299a0001c0001t0001g0356others(42): Show | 45 | HG00597.hp2 HG00642.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1658-277G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622181 | ||||||
| chr5:180622260
|
C | CCATCTCT others(19): Show |
3 | a0002c0002t0013g0165a0007c0010t0010g0323a0027c0042t0028g0379 | 3 | HG01243.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1658-382_1658-357d others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622260 | ||||||
| chr5:180622260
|
CCATCTCT others(19): Show |
C | 37 | a0001c0001t0001g0001a0001c0001t0001g0085a0001c0001t0001g0100others(34): Show | 39 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1658-382_1658-357d others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622260 | ||||||
| chr5:180622348
|
C | T | 113 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(110): Show | 116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1657+383G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622348 | ||||||
| chr5:180622410
|
G | A | 1 | a0002c0003t0003g0289 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1657+321C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622410 | ||||||
| chr5:180622432
|
G | A | 35 | a0001c0001t0001g0092a0001c0001t0001g0118a0001c0001t0001g0215others(32): Show | 35 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1657+299C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622432 | ||||||
| chr5:180622492
|
G | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0268a0001c0001t0005g0079 | 3 | NA18982.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1657+239C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622492 | ||||||
| chr5:180622525
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(220): Show | 229 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1657+206A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622525 | ||||||
| chr5:180622529
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1657+202C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622529 | ||||||
| chr5:180622618
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(188): Show | 195 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1657+113T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 12/29 | chr5 | 180622618 | ||||||
| chr5:180622907
|
G | A | 40 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0003g0338others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.1549-68C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622907 | ||||||
| chr5:180622923
|
G | T | 1 | a0001c0001t0002g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1549-84C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622923 | ||||||
| chr5:180622923
|
GCAC | G | 18 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0001g0360others(15): Show | 19 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1549-87_1549-85del others(3): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622923 | ||||||
| chr5:180622925
|
A | AC | 86 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0038others(83): Show | 87 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1549-87dupG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622925 | ||||||
| chr5:180622925
|
A | ACC | 13 | a0001c0001t0001g0035a0001c0001t0001g0194a0001c0001t0001g0226others(10): Show | 14 | HG00642.hp2 HG00738.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1549-88_1549-87dup others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622925 | ||||||
| chr5:180622926
|
CCA | C | 72 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0001g0118others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1549-89_1549-88del others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622926 | ||||||
| chr5:180622927
|
CA | C | 16 | a0001c0001t0001g0039a0001c0001t0001g0106a0001c0001t0001g0320others(13): Show | 16 | HG01069.hp1 HG01167.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1549-89delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622927 | ||||||
| chr5:180622928
|
A | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(251): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1549-89T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622928 | ||||||
| chr5:180622929
|
C | A | 1 | a0001c0001t0006g0292 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1549-90G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622929 | ||||||
| chr5:180622935
|
C | T | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1549-96G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622935 | ||||||
| chr5:180622942
|
TG | T | 7 | a0001c0001t0001g0360a0001c0001t0010g0368a0001c0001t0027g0231others(4): Show | 7 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1549-104delC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180622942 | ||||||
| chr5:180623066
|
T | C | 19 | a0002c0004t0003g0161a0002c0004t0005g0026a0002c0004t0005g0053others(16): Show | 19 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.1549-227A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623066 | ||||||
| chr5:180623148
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(258): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1549-309A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623148 | ||||||
| chr5:180623163
|
C | T | 60 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0001g0299others(57): Show | 62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1549-324G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623163 | ||||||
| chr5:180623208
|
A | G | 359 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(356): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1549-369T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623208 | ||||||
| chr5:180623310
|
C | T | 1 | a0002c0003t0019g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1549-471G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623310 | ||||||
| chr5:180623491
|
G | A | 1 | a0002c0003t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1548+444C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623491 | ||||||
| chr5:180623597
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0092 | 2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1548+338C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623597 | ||||||
| chr5:180623600
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0092 | 2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1548+335G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623600 | ||||||
| chr5:180623727
|
G | A | 1 | a0007c0010t0015g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1548+208C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623727 | ||||||
| chr5:180623816
|
C | T | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1548+119G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623816 | ||||||
| chr5:180623893
|
T | C | 1 | a0017c0049t0005g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1548+42A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 11/29 | chr5 | 180623893 | ||||||
| chr5:180624118
|
A | T | 55 | a0001c0001t0001g0118a0001c0001t0001g0215a0001c0001t0001g0360others(52): Show | 55 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1422-57T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624118 | ||||||
| chr5:180624127
|
G | A | 1 | a0009c0024t0001g0004 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1422-66C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624127 | ||||||
| chr5:180624227
|
G | GT | 78 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0139others(75): Show | 79 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1422-167dupA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624227 | ||||||
| chr5:180624227
|
G | GTT | 42 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1422-168_1422-167d others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624227 | ||||||
| chr5:180624296
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(311): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1422-235T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624296 | ||||||
| chr5:180624305
|
A | G | 41 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1422-244T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624305 | ||||||
| chr5:180624329
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1422-268G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624329 | ||||||
| chr5:180624447
|
C | T | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1422-386G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624447 | ||||||
| chr5:180624491
|
G | A | 3 | a0002c0003t0002g0325a0002c0003t0002g0336a0021c0034t0009g0287 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1422-430C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624491 | ||||||
| chr5:180624659
|
C | T | 5 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1422-598G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624659 | ||||||
| chr5:180624710
|
A | C | 33 | a0001c0001t0001g0070a0001c0001t0001g0118a0001c0001t0001g0215others(30): Show | 33 | HG00597.hp1 HG00673.hp2 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.1422-649T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624710 | ||||||
| chr5:180624713
|
G | A | 4 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422-652C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624713 | ||||||
| chr5:180624814
|
T | C | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1422-753A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624814 | ||||||
| chr5:180624934
|
C | A | 71 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1422-873G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624934 | ||||||
| chr5:180624937
|
G | T | 22 | a0001c0001t0003g0338a0001c0001t0004g0078a0002c0002t0001g0072others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1422-876C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624937 | ||||||
| chr5:180624987
|
T | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0118others(57): Show | 61 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1421+882A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624987 | ||||||
| chr5:180624991
|
G | A | 1 | a0002c0029t0001g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1421+878C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180624991 | ||||||
| chr5:180625041
|
T | G | 359 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(356): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1421+828A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625041 | ||||||
| chr5:180625108
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(230): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1421+761G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625108 | ||||||
| chr5:180625120
|
C | T | 1 | a0002c0004t0005g0232 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1421+749G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625120 | ||||||
| chr5:180625247
|
G | A | 4 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1421+622C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625247 | ||||||
| chr5:180625259
|
C | T | 1 | a0016c0051t0002g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1421+610G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625259 | ||||||
| chr5:180625292
|
C | T | 1 | a0002c0003t0003g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1421+577G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625292 | ||||||
| chr5:180625298
|
G | A | 1 | a0002c0002t0004g0064 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1421+571C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625298 | ||||||
| chr5:180625410
|
G | A | 1 | a0002c0011t0004g0007 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1421+459C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625410 | ||||||
| chr5:180625513
|
C | T | 1 | a0007c0010t0001g0245 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1421+356G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625513 | ||||||
| chr5:180625580
|
G | A | 5 | a0002c0002t0013g0165a0002c0003t0010g0043a0002c0003t0010g0178others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421+289C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625580 | ||||||
| chr5:180625694
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1421+175G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625694 | ||||||
| chr5:180625806
|
T | G | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1421+63A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625806 | ||||||
| chr5:180625817
|
G | A | 23 | a0001c0013t0001g0146a0001c0013t0001g0150a0001c0013t0001g0151others(20): Show | 23 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1421+52C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625817 | ||||||
| chr5:180625831
|
TGGCTGTG others(12): Show |
T | 39 | a0001c0001t0001g0118a0001c0001t0001g0215a0001c0001t0001g0360others(36): Show | 39 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1421+19_1421+37del others(19): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625831 | ||||||
| chr5:180625832
|
G | A | 3 | a0002c0003t0007g0006a0002c0012t0001g0052a0002c0012t0023g0045 | 4 | HG02280.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421+37C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 10/29 | chr5 | 180625832 | ||||||
| chr5:180626085
|
C | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258+26G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 9/29 | chr5 | 180626085 | ||||||
| chr5:180626090
|
G | A | 41 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1258+21C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 9/29 | chr5 | 180626090 | ||||||
| chr5:180626095
|
C | T | 1 | a0002c0003t0007g0369 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1258+16G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 9/29 | chr5 | 180626095 | ||||||
| chr5:180626097
|
C | T | 41 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1258+14G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 9/29 | chr5 | 180626097 | ||||||
| chr5:180626307
|
A | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(355): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1104-42T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626307 | ||||||
| chr5:180626327
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1104-62C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626327 | ||||||
| chr5:180626358
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1104-93C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626358 | ||||||
| chr5:180626387
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(156): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1104-122G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626387 | ||||||
| chr5:180626478
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1104-213G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626478 | ||||||
| chr5:180626616
|
G | A | 1 | a0006c0014t0002g0374 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1104-351C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626616 | ||||||
| chr5:180626621
|
C | G | 4 | a0001c0013t0001g0146a0001c0013t0001g0150a0001c0013t0001g0151others(1): Show | 4 | HG00673.hp1 NA18951.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104-356G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626621 | ||||||
| chr5:180626637
|
C | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0002c0029t0001g0228 | 3 | HG00438.hp1 HG00609.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1104-372G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626637 | ||||||
| chr5:180626671
|
T | C | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1104-406A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626671 | ||||||
| chr5:180626672
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1104-407G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626672 | ||||||
| chr5:180626722
|
C | T | 71 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1104-457G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626722 | ||||||
| chr5:180626777
|
C | T | 11 | a0001c0001t0001g0091a0001c0001t0001g0133a0001c0001t0001g0135others(8): Show | 11 | NA18945.hp1 NA18947.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.1104-512G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626777 | ||||||
| chr5:180626794
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(357): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1104-529A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626794 | ||||||
| chr5:180626795
|
G | A | 14 | a0001c0001t0001g0309a0001c0001t0002g0300a0001c0001t0002g0310others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1104-530C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626795 | ||||||
| chr5:180626851
|
G | A | 2 | a0001c0001t0001g0360a0001c0001t0027g0231 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1104-586C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626851 | ||||||
| chr5:180626913
|
G | A | 23 | a0001c0013t0001g0146a0001c0013t0001g0150a0001c0013t0001g0151others(20): Show | 23 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1104-648C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626913 | ||||||
| chr5:180626955
|
C | G | 1 | a0002c0012t0023g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1104-690G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626955 | ||||||
| chr5:180626955
|
C | T | 4 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1104-690G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626955 | ||||||
| chr5:180626959
|
C | T | 15 | a0001c0001t0001g0299a0001c0001t0001g0309a0001c0001t0002g0300others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1104-694G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180626959 | ||||||
| chr5:180627024
|
C | T | 41 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0085others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1104-759G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627024 | ||||||
| chr5:180627220
|
T | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(355): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1104-955A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627220 | ||||||
| chr5:180627227
|
G | A | 2 | a0003c0005t0002g0042a0019c0040t0002g0046 | 2 | HG00642.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1104-962C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627227 | ||||||
| chr5:180627305
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1104-1040G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627305 | ||||||
| chr5:180627324
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1104-1059C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627324 | ||||||
| chr5:180627344
|
G | A | 2 | a0003c0005t0001g0036a0003c0005t0001g0037 | 2 | HG01069.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1104-1079C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627344 | ||||||
| chr5:180627394
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1104-1129A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627394 | ||||||
| chr5:180627449
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1104-1184A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627449 | ||||||
| chr5:180627465
|
C | T | 1 | a0001c0001t0003g0338 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1104-1200G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627465 | ||||||
| chr5:180627548
|
GT | G | 24 | a0001c0001t0001g0168a0001c0001t0002g0300a0002c0003t0001g0375others(21): Show | 24 | HG00642.hp1 HG01516.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1104-1284delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627548 | ||||||
| chr5:180627560
|
G | A | 1 | a0001c0043t0002g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1104-1295C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627560 | ||||||
| chr5:180627709
|
G | T | 2 | a0001c0001t0027g0231a0002c0003t0001g0370 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1103+1173C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627709 | ||||||
| chr5:180627711
|
C | T | 147 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1103+1171G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627711 | ||||||
| chr5:180627773
|
C | T | 1 | a0002c0003t0005g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1103+1109G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627773 | ||||||
| chr5:180627778
|
A | G | 1 | a0002c0003t0010g0043 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1103+1104T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627778 | ||||||
| chr5:180627853
|
A | T | 46 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0001g0215others(43): Show | 46 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1103+1029T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180627853 | ||||||
| chr5:180628136
|
T | C | 1 | a0001c0006t0001g0282 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1103+746A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628136 | ||||||
| chr5:180628188
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(114): Show | 121 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1103+694T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628188 | ||||||
| chr5:180628258
|
T | C | 21 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0200others(18): Show | 21 | HG00597.hp2 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1103+624A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628258 | ||||||
| chr5:180628259
|
G | A | 21 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0200others(18): Show | 21 | HG00597.hp2 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1103+623C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628259 | ||||||
| chr5:180628278
|
C | G | 1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103+604G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628278 | ||||||
| chr5:180628288
|
G | A | 1 | a0001c0009t0014g0083 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1103+594C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628288 | ||||||
| chr5:180628304
|
G | A | 4 | a0002c0008t0004g0296a0002c0008t0004g0324a0002c0008t0032g0305others(1): Show | 4 | NA18939.hp2 NA19065.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103+578C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628304 | ||||||
| chr5:180628411
|
T | C | 77 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0057others(74): Show | 79 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1103+471A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628411 | ||||||
| chr5:180628441
|
C | G | 21 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0200others(18): Show | 21 | HG00597.hp2 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1103+441G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628441 | ||||||
| chr5:180628511
|
C | T | 1 | a0001c0001t0006g0363 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1103+371G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628511 | ||||||
| chr5:180628573
|
G | A | 1 | a0002c0004t0005g0232 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1103+309C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628573 | ||||||
| chr5:180628631
|
C | T | 21 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0200others(18): Show | 21 | HG00597.hp2 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1103+251G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628631 | ||||||
| chr5:180628656
|
G | A | 1 | a0002c0003t0001g0321 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1103+226C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628656 | ||||||
| chr5:180628742
|
C | T | 1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1103+140G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628742 | ||||||
| chr5:180628774
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG03017.hp2 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1103+108C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628774 | ||||||
| chr5:180628849
|
T | G | 59 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0106others(56): Show | 59 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1103+33A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628849 | ||||||
| chr5:180628859
|
C | CG | 3 | a0002c0002t0001g0256a0002c0002t0004g0266a0002c0035t0001g0221 | 3 | HG03654.hp1 HG03927.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1103+22dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628859 | ||||||
| chr5:180628862
|
T | C | 32 | a0001c0006t0001g0154a0001c0006t0001g0157a0001c0006t0001g0158others(29): Show | 32 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1103+20A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628862 | ||||||
| chr5:180628862
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(236): Show | 244 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1103+20A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628862 | ||||||
| chr5:180628864
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(156): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1103+18C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 8/29 | chr5 | 180628864 | ||||||
| chr5:180629017
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.986-18A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 7/29 | chr5 | 180629017 | ||||||
| chr5:180629044
|
G | A | 74 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0057others(71): Show | 76 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.986-45C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 7/29 | chr5 | 180629044 | ||||||
| chr5:180629192
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(156): Show | 164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.985+67A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 7/29 | chr5 | 180629192 | ||||||
| chr5:180629215
|
C | T | 1 | a0002c0035t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.985+44G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 7/29 | chr5 | 180629215 | ||||||
| chr5:180629453
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0002g0300 | 2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.817-26C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629453 | ||||||
| chr5:180629522
|
C | T | 5 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-95G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629522 | ||||||
| chr5:180629565
|
A | G | 1 | a0026c0030t0030g0303 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.816+131T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629565 | ||||||
| chr5:180629581
|
G | C | 21 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0200others(18): Show | 21 | HG00597.hp2 HG01175.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.816+115C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629581 | ||||||
| chr5:180629620
|
G | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(347): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.816+76C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629620 | ||||||
| chr5:180629621
|
C | T | 3 | a0002c0003t0002g0325a0002c0003t0002g0336a0021c0034t0009g0287 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.816+75G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 6/29 | chr5 | 180629621 | ||||||
| chr5:180629848
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-13T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 5/29 | chr5 | 180629848 | ||||||
| chr5:180629863
|
C | T | 16 | a0001c0023t0008g0377a0001c0023t0008g0378a0002c0002t0001g0351others(13): Show | 16 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.677-28G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 5/29 | chr5 | 180629863 | ||||||
| chr5:180630120
|
C | T | 1 | a0016c0051t0002g0276 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.514-15G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/29 | chr5 | 180630120 | ||||||
| chr5:180630167
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.513+58G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 4/29 | chr5 | 180630167 | ||||||
| chr5:180630356
|
C | G | 87 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0062others(84): Show | 88 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.401-19G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630356 | ||||||
| chr5:180630371
|
C | T | 3 | a0001c0001t0012g0357a0001c0001t0012g0358a0029c0028t0010g0179 | 3 | HG00280.hp2 HG00323.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.401-34G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630371 | ||||||
| chr5:180630433
|
C | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0118others(8): Show | 11 | HG00423.hp2 HG00597.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.401-96G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630433 | ||||||
| chr5:180630496
|
C | T | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.400+59G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630496 | ||||||
| chr5:180630504
|
G | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(65): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.400+51C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630504 | ||||||
| chr5:180630505
|
C | A | 1 | a0001c0009t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.400+50G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630505 | ||||||
| chr5:180630516
|
C | T | 1 | a0001c0001t0001g0365 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+39G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630516 | ||||||
| chr5:180630538
|
C | T | 42 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0106others(39): Show | 42 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.400+17G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 3/29 | chr5 | 180630538 | ||||||
| chr5:180630859
|
A | AGAAGCCT others(7): Show |
1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.156-74_156-61dupCT others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180630859 | ||||||
| chr5:180630876
|
C | T | 27 | a0001c0001t0001g0062a0001c0001t0002g0206a0001c0001t0004g0131others(24): Show | 27 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.156-77G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180630876 | ||||||
| chr5:180630935
|
C | T | 1 | a0004c0007t0001g0017 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.156-136G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180630935 | ||||||
| chr5:180630943
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.156-144G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180630943 | ||||||
| chr5:180631007
|
G | A | 2 | a0001c0001t0002g0048a0001c0032t0026g0333 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.156-208C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631007 | ||||||
| chr5:180631008
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(312): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.156-209G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631008 | ||||||
| chr5:180631011
|
A | G | 18 | a0001c0001t0001g0309a0001c0001t0002g0048a0001c0001t0002g0208others(15): Show | 18 | HG01243.hp1 HG02145.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.156-212T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631011 | ||||||
| chr5:180631049
|
T | G | 1 | a0002c0002t0001g0081 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.156-250A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631049 | ||||||
| chr5:180631050
|
A | T | 1 | a0002c0002t0001g0081 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.156-251T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631050 | ||||||
| chr5:180631050
|
AC | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0039others(88): Show | 94 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.156-252delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631050 | ||||||
| chr5:180631051
|
C | A | 1 | a0002c0002t0001g0081 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.156-252G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631051 | ||||||
| chr5:180631081
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.156-282T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631081 | ||||||
| chr5:180631083
|
G | C | 30 | a0001c0001t0001g0184a0001c0001t0001g0309a0001c0001t0002g0047others(27): Show | 31 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.156-284C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631083 | ||||||
| chr5:180631189
|
G | A | 9 | a0002c0004t0005g0053a0002c0004t0005g0054a0003c0005t0001g0034others(6): Show | 9 | HG00099.hp2 HG01069.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-390C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631189 | ||||||
| chr5:180631200
|
A | G | 5 | a0002c0003t0001g0375a0002c0003t0010g0043a0002c0003t0010g0178others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-401T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631200 | ||||||
| chr5:180631202
|
A | G | 6 | a0002c0002t0001g0125a0002c0003t0001g0375a0002c0003t0010g0043others(3): Show | 6 | HG01175.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-403T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631202 | ||||||
| chr5:180631223
|
C | T | 1 | a0001c0006t0001g0282 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.156-424G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631223 | ||||||
| chr5:180631228
|
C | A | 7 | a0001c0001t0012g0357a0001c0001t0012g0358a0002c0002t0001g0351others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-429G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631228 | ||||||
| chr5:180631239
|
T | C | 20 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(17): Show | 20 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.156-440A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631239 | ||||||
| chr5:180631244
|
T | C | 26 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(23): Show | 26 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.155+438A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631244 | ||||||
| chr5:180631248
|
T | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(19): Show | 22 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.155+434A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631248 | ||||||
| chr5:180631249
|
G | A | 2 | a0001c0001t0002g0307a0002c0003t0002g0286 | 2 | HG01952.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.155+433C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631249 | ||||||
| chr5:180631251
|
G | A | 22 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(19): Show | 22 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.155+431C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631251 | ||||||
| chr5:180631253
|
T | C | 22 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(19): Show | 22 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.155+429A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631253 | ||||||
| chr5:180631270
|
A | G | 15 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(12): Show | 15 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.155+412T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631270 | ||||||
| chr5:180631282
|
C | G | 13 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(10): Show | 13 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+400G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631282 | ||||||
| chr5:180631283
|
T | C | 13 | a0001c0001t0001g0121a0001c0001t0001g0197a0001c0001t0001g0198others(10): Show | 13 | HG01175.hp2 HG01256.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+399A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631283 | ||||||
| chr5:180631284
|
T | C | 1 | a0001c0001t0006g0292 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.155+398A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631284 | ||||||
| chr5:180631298
|
C | T | 7 | a0001c0001t0001g0121a0001c0001t0002g0206a0001c0001t0006g0122others(4): Show | 7 | HG01175.hp2 HG01358.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.155+384G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631298 | ||||||
| chr5:180631311
|
C | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155+371G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631311 | ||||||
| chr5:180631312
|
A | G | 9 | a0001c0001t0001g0168a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.155+370T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631312 | ||||||
| chr5:180631327
|
G | T | 1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155+355C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631327 | ||||||
| chr5:180631342
|
G | A | 2 | a0001c0009t0002g0114a0002c0003t0007g0373 | 2 | HG02970.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.155+340C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631342 | ||||||
| chr5:180631365
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0009t0004g0013others(1): Show | 4 | HG04184.hp1 NA18994.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.155+317A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631365 | ||||||
| chr5:180631389
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.155+293G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631389 | ||||||
| chr5:180631390
|
G | C | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.155+292C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631390 | ||||||
| chr5:180631405
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0004g0142a0001c0001t0024g0105others(3): Show | 6 | HG02027.hp1 HG02155.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+277T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631405 | ||||||
| chr5:180631408
|
G | A | 1 | a0002c0002t0014g0031 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.155+274C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631408 | ||||||
| chr5:180631409
|
C | G | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.155+273G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631409 | ||||||
| chr5:180631423
|
A | G | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.155+259T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631423 | ||||||
| chr5:180631430
|
A | G | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.155+252T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631430 | ||||||
| chr5:180631433
|
A | C | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.155+249T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631433 | ||||||
| chr5:180631451
|
T | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(353): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.155+231A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631451 | ||||||
| chr5:180631459
|
T | C | 5 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0003t0007g0314others(2): Show | 5 | HG02717.hp2 HG03471.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.155+223A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631459 | ||||||
| chr5:180631468
|
A | G | 2 | a0005c0015t0011g0171a0005c0015t0011g0172 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.155+214T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631468 | ||||||
| chr5:180631504
|
T | A | 1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.155+178A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631504 | ||||||
| chr5:180631556
|
G | A | 3 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0218 | 3 | NA18941.hp2 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.155+126C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631556 | ||||||
| chr5:180631562
|
G | A | 2 | a0001c0001t0010g0368a0002c0003t0001g0370 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.155+120C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631562 | ||||||
| chr5:180631591
|
G | A | 2 | a0001c0001t0012g0005a0001c0001t0012g0223 | 3 | HG00639.hp2 HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.155+91C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 2/29 | chr5 | 180631591 | ||||||
| chr5:180631802
|
G | A | 3 | a0001c0001t0010g0368a0002c0003t0001g0370a0027c0042t0028g0379 | 3 | HG02647.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.59-24C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631802 | ||||||
| chr5:180631842
|
T | C | 29 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0006t0001g0154others(26): Show | 29 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-64A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631842 | ||||||
| chr5:180631911
|
CCGCGTGG others(8): Show |
C | 180 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(177): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.59-148_59-134delAG others(13): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631911 | ||||||
| chr5:180631928
|
A | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(177): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.59-150T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631928 | ||||||
| chr5:180631940
|
G | A | 2 | a0002c0003t0007g0314a0002c0003t0007g0315 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.59-162C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631940 | ||||||
| chr5:180631951
|
C | G | 1 | a0002c0004t0005g0232 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-173G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631951 | ||||||
| chr5:180631962
|
C | T | 1 | a0002c0003t0003g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.59-184G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631962 | ||||||
| chr5:180631963
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(177): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.59-185C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180631963 | ||||||
| chr5:180632042
|
T | C | 16 | a0001c0001t0001g0038a0001c0001t0003g0050a0001c0001t0006g0051others(13): Show | 16 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-264A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632042 | ||||||
| chr5:180632097
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.59-319C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632097 | ||||||
| chr5:180632107
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(19): Show | 22 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-329G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632107 | ||||||
| chr5:180632117
|
T | C | 3 | a0001c0032t0026g0333a0005c0018t0013g0167a0027c0042t0028g0379 | 3 | HG02257.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.59-339A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632117 | ||||||
| chr5:180632134
|
G | A | 28 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-356C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632134 | ||||||
| chr5:180632140
|
T | G | 1 | a0006c0033t0009g0376 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-362A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632140 | ||||||
| chr5:180632228
|
C | T | 2 | a0001c0001t0001g0309a0002c0003t0007g0369 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-450G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632228 | ||||||
| chr5:180632230
|
A | C | 377 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(374): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.59-452T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632230 | ||||||
| chr5:180632238
|
A | AGGCCTCG others(26): Show |
28 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(25): Show | 28 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-493_59-461dupCC others(31): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632238 | ||||||
| chr5:180632238
|
A | AGGCCTCG others(92): Show |
1 | a0002c0004t0005g0232 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-461_59-460insCC others(97): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632238 | ||||||
| chr5:180632238
|
AGGCCTCG others(26): Show |
A | 1 | a0001c0001t0025g0265 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.59-493_59-461delCC others(31): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632238 | ||||||
| chr5:180632246
|
C | T | 153 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(150): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.59-468G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632246 | ||||||
| chr5:180632259
|
G | A | 2 | a0001c0001t0002g0066a0002c0008t0004g0065 | 2 | NA18971.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.59-481C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632259 | ||||||
| chr5:180632279
|
C | T | 2 | a0001c0001t0002g0107a0002c0003t0003g0108 | 2 | HG00673.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.59-501G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632279 | ||||||
| chr5:180632284
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.59-506A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632284 | ||||||
| chr5:180632354
|
C | T | 2 | a0001c0001t0002g0047a0018c0039t0001g0040 | 2 | HG01884.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.59-576G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632354 | ||||||
| chr5:180632424
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(144): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.59-646T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632424 | ||||||
| chr5:180632596
|
GGTGGTGT others(6): Show |
G | 1 | a0002c0002t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.59-831_59-819delAC others(11): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632596 | ||||||
| chr5:180632599
|
GGT | G | 20 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0050others(17): Show | 20 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-823_59-822delAC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGT | G | 8 | a0001c0001t0002g0047a0001c0001t0002g0048a0002c0004t0005g0145others(5): Show | 8 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-825_59-822delAC others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGT | G | 4 | a0001c0001t0001g0062a0001c0001t0002g0049a0002c0004t0005g0156others(1): Show | 4 | HG02602.hp1 HG03209.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-827_59-822delAC others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(1): Show |
G | 19 | a0001c0006t0001g0154a0001c0006t0001g0157a0001c0006t0001g0282others(16): Show | 19 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.59-829_59-822delAC others(6): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(3): Show |
G | 16 | a0001c0001t0001g0113a0001c0001t0002g0371a0001c0001t0002g0372others(13): Show | 16 | HG00741.hp1 HG01934.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-831_59-822delAC others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(5): Show |
G | 120 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(117): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.59-833_59-822delAC others(10): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(7): Show |
G | 168 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(165): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.59-835_59-822delAC others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(9): Show |
G | 3 | a0001c0001t0001g0309a0001c0032t0026g0333a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.59-837_59-822delAC others(14): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632599
|
GGTGTGTG others(11): Show |
G | 3 | a0001c0047t0001g0173a0002c0003t0001g0375a0005c0015t0011g0171 | 3 | HG02809.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.59-839_59-822delAC others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632599 | ||||||
| chr5:180632600
|
GTGTGTGT others(6): Show |
G | 1 | a0002c0035t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.59-835_59-823delAC others(11): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632600 | ||||||
| chr5:180632633
|
T | C | 2 | a0001c0001t0003g0050a0001c0001t0006g0051 | 2 | HG00408.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.59-855A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632633 | ||||||
| chr5:180632635
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0003g0050a0001c0001t0006g0051others(1): Show | 4 | HG00408.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-857A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632635 | ||||||
| chr5:180632657
|
C | T | 1 | a0002c0002t0004g0094 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.59-879G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632657 | ||||||
| chr5:180632659
|
T | C | 1 | a0002c0002t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-881A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632659 | ||||||
| chr5:180632746
|
T | G | 1 | a0002c0011t0014g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-968A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632746 | ||||||
| chr5:180632789
|
T | C | 1 | a0002c0003t0007g0369 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.59-1011A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632789 | ||||||
| chr5:180632824
|
G | A | 2 | a0001c0001t0012g0005a0001c0001t0012g0223 | 3 | HG00639.hp2 HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.59-1046C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632824 | ||||||
| chr5:180632876
|
C | T | 1 | a0001c0052t0001g0153 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.59-1098G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180632876 | ||||||
| chr5:180633019
|
T | TG | 22 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(19): Show | 22 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-1242dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633019 | ||||||
| chr5:180633080
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-1302G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633080 | ||||||
| chr5:180633173
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.59-1395G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633173 | ||||||
| chr5:180633262
|
A | G | 1 | a0001c0001t0029g0260 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.59-1484T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633262 | ||||||
| chr5:180633449
|
G | T | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-1671C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633449 | ||||||
| chr5:180633450
|
T | G | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-1672A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633450 | ||||||
| chr5:180633451
|
G | T | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-1673C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633451 | ||||||
| chr5:180633473
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.59-1695A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633473 | ||||||
| chr5:180633473
|
T | TG | 326 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(323): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.59-1696dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633473 | ||||||
| chr5:180633505
|
G | A | 1 | a0001c0001t0012g0358 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.59-1727C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633505 | ||||||
| chr5:180633527
|
G | A | 4 | a0001c0047t0001g0173a0002c0003t0001g0375a0005c0015t0011g0171others(1): Show | 4 | HG02572.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-1749C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633527 | ||||||
| chr5:180633562
|
C | T | 1 | a0002c0002t0001g0097 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.59-1784G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633562 | ||||||
| chr5:180633674
|
G | A | 1 | a0022c0045t0005g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.59-1896C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633674 | ||||||
| chr5:180633707
|
C | G | 10 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(7): Show | 10 | HG02257.hp2 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-1929G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633707 | ||||||
| chr5:180633790
|
C | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(330): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.59-2012G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633790 | ||||||
| chr5:180633795
|
G | A | 3 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.59-2017C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633795 | ||||||
| chr5:180633804
|
G | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(145): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.59-2026C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633804 | ||||||
| chr5:180633988
|
G | A | 149 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(146): Show | 150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.59-2210C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180633988 | ||||||
| chr5:180634025
|
C | A | 1 | a0022c0045t0005g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.59-2247G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634025 | ||||||
| chr5:180634120
|
C | T | 139 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0057others(136): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.59-2342G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634120 | ||||||
| chr5:180634191
|
C | T | 6 | a0001c0001t0002g0371a0001c0001t0002g0372a0002c0003t0001g0317others(3): Show | 6 | HG02809.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-2413G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634191 | ||||||
| chr5:180634395
|
C | T | 1 | a0002c0002t0001g0337 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.59-2617G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634395 | ||||||
| chr5:180634414
|
A | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(330): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.59-2636T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634414 | ||||||
| chr5:180634570
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.59-2792G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634570 | ||||||
| chr5:180634600
|
C | CG | 6 | a0001c0001t0001g0121a0001c0001t0001g0130a0001c0001t0001g0272others(3): Show | 6 | HG03516.hp2 HG03710.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-2823dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634600 | ||||||
| chr5:180634626
|
C | T | 27 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(24): Show | 27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-2848G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634626 | ||||||
| chr5:180634694
|
CA | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(254): Show | 265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.59-2917delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634694 | ||||||
| chr5:180634694
|
CAA | C | 69 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0118others(66): Show | 69 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.59-2918_59-2917del others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634694 | ||||||
| chr5:180634698
|
A | C | 1 | a0002c0003t0002g0325 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.59-2920T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634698 | ||||||
| chr5:180634699
|
A | C | 1 | a0002c0003t0002g0336 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.59-2921T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634699 | ||||||
| chr5:180634801
|
G | GATGGGTG others(41): Show |
1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-3024_59-3023ins others(48): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634801 | ||||||
| chr5:180634801
|
GATGGGTG others(49): Show |
G | 14 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0312others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3079_59-3024del others(56): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634801 | ||||||
| chr5:180634806
|
GTGGA | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(288): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.59-3032_59-3029del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634806 | ||||||
| chr5:180634810
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3032T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634810 | ||||||
| chr5:180634810
|
ATGGG | A | 43 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(40): Show | 43 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.59-3036_59-3033del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634810 | ||||||
| chr5:180634812
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3034C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634812 | ||||||
| chr5:180634816
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(288): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.59-3038C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634816 | ||||||
| chr5:180634818
|
G | A | 1 | a0002c0004t0003g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.59-3040C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634818 | ||||||
| chr5:180634820
|
G | C | 2 | a0001c0001t0001g0268a0001c0001t0005g0079 | 2 | NA18982.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.59-3042C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634820 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(261): Show |
1 | a0001c0001t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(268): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(473): Show |
1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(480): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(313): Show |
1 | a0002c0002t0014g0031 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(320): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(262): Show |
1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(269): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(401): Show |
1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(408): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(980): Show |
1 | a0001c0009t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(987): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(253): Show |
1 | a0002c0008t0004g0324 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(260): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(365): Show |
1 | a0002c0038t0004g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(372): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(261): Show |
11 | a0001c0001t0002g0217a0001c0001t0002g0218a0002c0002t0001g0030others(8): Show | 11 | HG00280.hp1 HG01123.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3046_59-3045ins others(268): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(361): Show |
1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(368): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(221): Show |
1 | a0001c0009t0004g0013 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(228): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634823
|
T | TGGGAGGA others(265): Show |
1 | a0001c0001t0001g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.59-3046_59-3045ins others(272): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634823 | ||||||
| chr5:180634830
|
GAGGA | G | 3 | a0002c0004t0003g0161a0002c0022t0003g0147a0002c0022t0003g0148 | 3 | NA18995.hp1 NA19012.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.59-3056_59-3053del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634830 | ||||||
| chr5:180634831
|
A | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(19): Show | 22 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-3053T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634831 | ||||||
| chr5:180634851
|
T | C | 1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-3073A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634851 | ||||||
| chr5:180634854
|
A | AAGTATGG others(573): Show |
1 | a0002c0002t0001g0081 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.59-3077_59-3076ins others(580): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634854 | ||||||
| chr5:180634857
|
T | TATGGGTG others(29): Show |
1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-3080_59-3079ins others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634857 | ||||||
| chr5:180634866
|
A | ATGGGTGG others(217): Show |
1 | a0001c0001t0004g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.59-3089_59-3088ins others(224): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634866 | ||||||
| chr5:180634866
|
A | G | 14 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0312others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3088T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634866 | ||||||
| chr5:180634866
|
ATGGGTGG others(1): Show |
A | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3096_59-3089del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634866 | ||||||
| chr5:180634868
|
G | A | 14 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0002g0312others(11): Show | 15 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3090C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634868 | ||||||
| chr5:180634870
|
G | GTGGATGG others(73): Show |
2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3093_59-3092ins others(80): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634870 | ||||||
| chr5:180634870
|
G | GTGGATGG others(121): Show |
1 | a0002c0008t0004g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.59-3093_59-3092ins others(128): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634870 | ||||||
| chr5:180634870
|
G | GTGGATGG others(29): Show |
1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3093_59-3092ins others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634870 | ||||||
| chr5:180634873
|
GGTGGGTG others(13): Show |
G | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-3115_59-3096del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634873 | ||||||
| chr5:180634874
|
G | A | 44 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0091others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.59-3096C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
G | GTGGGTGG others(29): Show |
1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3097_59-3096ins others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
G | GTGGGTGG others(93): Show |
1 | a0001c0001t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.59-3097_59-3096ins others(100): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
G | GTGGGTGG others(77): Show |
27 | a0001c0001t0001g0062a0001c0001t0001g0320a0001c0006t0001g0154others(24): Show | 27 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-3097_59-3096ins others(84): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
G | GTGGGTGG others(821): Show |
1 | a0001c0001t0012g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59-3097_59-3096ins others(828): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
G | GTGGGTGG others(85): Show |
1 | a0003c0005t0001g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.59-3097_59-3096ins others(92): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634874
|
GTGGGTGG others(65): Show |
G | 4 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0295others(1): Show | 4 | HG02129.hp1 NA18948.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3168_59-3097del others(72): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634874 | ||||||
| chr5:180634877
|
GGTGGGTG others(6): Show |
G | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3112_59-3100del others(13): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634877 | ||||||
| chr5:180634878
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3100C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634878 | ||||||
| chr5:180634878
|
GTGGGTGG others(1): Show |
G | 143 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(140): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.59-3108_59-3101del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634878 | ||||||
| chr5:180634881
|
G | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(19): Show | 22 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-3103C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634881 | ||||||
| chr5:180634881
|
GGTGGATG others(5): Show |
G | 47 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.59-3115_59-3104del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634881 | ||||||
| chr5:180634882
|
G | A | 8 | a0001c0001t0001g0360a0001c0001t0002g0082a0001c0001t0002g0123others(5): Show | 8 | HG01952.hp2 HG02273.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3104C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634882 | ||||||
| chr5:180634882
|
GTGGATGG others(5): Show |
G | 1 | a0002c0002t0004g0266 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.59-3116_59-3105del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634882 | ||||||
| chr5:180634883
|
T | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0129others(37): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.59-3105A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634883 | ||||||
| chr5:180634885
|
G | C | 6 | a0001c0001t0001g0360a0001c0001t0002g0082a0001c0001t0002g0123others(3): Show | 6 | HG01952.hp2 HG02273.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3107C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634885 | ||||||
| chr5:180634886
|
A | ATGGATGC others(33): Show |
2 | a0002c0022t0003g0147a0002c0022t0003g0148 | 2 | NA18995.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.59-3109_59-3108ins others(40): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634886 | ||||||
| chr5:180634886
|
A | ATGGATGC others(45): Show |
1 | a0002c0002t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.59-3109_59-3108ins others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634886 | ||||||
| chr5:180634886
|
A | ATGGATGC others(37): Show |
2 | a0007c0010t0010g0323a0014c0020t0013g0271 | 2 | HG01243.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.59-3152_59-3109dup others(44): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634886 | ||||||
| chr5:180634886
|
A | G | 37 | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0075others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-3108T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634886 | ||||||
| chr5:180634890
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG03688.hp2 NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3112T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634890 | ||||||
| chr5:180634891
|
T | A | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3113A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634891 | ||||||
| chr5:180634891
|
T | C | 1 | a0002c0003t0003g0095 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.59-3113A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634891 | ||||||
| chr5:180634893
|
C | G | 16 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0360others(13): Show | 16 | HG00597.hp1 HG00741.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-3115G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634893 | ||||||
| chr5:180634893
|
C | T | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3115G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634893 | ||||||
| chr5:180634893
|
CATGG | C | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-3119_59-3116del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634893 | ||||||
| chr5:180634895
|
T | A | 1 | a0002c0003t0003g0095 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.59-3117A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634895 | ||||||
| chr5:180634897
|
G | C | 4 | a0001c0001t0001g0075a0002c0002t0013g0165a0002c0003t0003g0362others(1): Show | 4 | HG00597.hp1 HG00741.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3119C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634897 | ||||||
| chr5:180634897
|
G | GAAGTATG others(77): Show |
1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3120_59-3119ins others(84): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634897 | ||||||
| chr5:180634897
|
G | GAGGGAAG others(329): Show |
1 | a0002c0003t0001g0321 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59-3120_59-3119ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634897 | ||||||
| chr5:180634897
|
G | T | 1 | a0002c0003t0003g0095 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.59-3119C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634897 | ||||||
| chr5:180634898
|
A | G | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3120T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634898 | ||||||
| chr5:180634899
|
T | A | 5 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(2): Show | 5 | HG01952.hp2 HG02273.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3121A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634899 | ||||||
| chr5:180634899
|
T | G | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3121A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634899 | ||||||
| chr5:180634901
|
G | GAAGT | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3124_59-3123ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634901 | ||||||
| chr5:180634901
|
G | T | 6 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(3): Show | 6 | HG01952.hp2 HG02273.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3123C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634901 | ||||||
| chr5:180634901
|
GATGGAAG others(1): Show |
G | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3131_59-3124del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634901 | ||||||
| chr5:180634902
|
A | G | 1 | a0002c0003t0003g0095 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.59-3124T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634902 | ||||||
| chr5:180634903
|
T | C | 5 | a0001c0001t0002g0216a0001c0001t0004g0078a0001c0001t0004g0142others(2): Show | 5 | HG02027.hp1 NA19079.hp1 NA19084.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3125A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634903 | ||||||
| chr5:180634903
|
T | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(28): Show | 31 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.59-3125A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634903 | ||||||
| chr5:180634906
|
A | G | 8 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(5): Show | 8 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3128T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634906 | ||||||
| chr5:180634907
|
A | T | 8 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(5): Show | 8 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3129T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634907 | ||||||
| chr5:180634909
|
T | G | 8 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(5): Show | 8 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3131A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634909 | ||||||
| chr5:180634917
|
GATGGGTG others(33): Show |
G | 2 | a0002c0002t0004g0203a0002c0002t0004g0204 | 2 | NA18993.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.59-3179_59-3140del others(40): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634917 | ||||||
| chr5:180634918
|
A | ATGGG | 3 | a0001c0001t0002g0216a0002c0002t0004g0033a0002c0008t0004g0296 | 3 | NA19079.hp1 NA19084.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3144_59-3141dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634918 | ||||||
| chr5:180634918
|
A | G | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3140T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634918 | ||||||
| chr5:180634918
|
ATGGG | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0092a0002c0004t0031g0279others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3144_59-3141del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634918 | ||||||
| chr5:180634926
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.59-3148C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634926 | ||||||
| chr5:180634929
|
G | GATGGAAG others(45): Show |
1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3152_59-3151ins others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634929 | ||||||
| chr5:180634930
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0002g0275 | 2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.59-3152C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634930 | ||||||
| chr5:180634930
|
GTGGGTGG others(57): Show |
G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-3216_59-3153del others(64): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634930 | ||||||
| chr5:180634931
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-3153A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634931 | ||||||
| chr5:180634934
|
G | A | 5 | a0001c0001t0002g0275a0001c0001t0006g0343a0002c0002t0001g0072others(2): Show | 5 | HG02717.hp2 HG03017.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3156C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634934 | ||||||
| chr5:180634935
|
T | A | 32 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0075others(29): Show | 32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-3157A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634935 | ||||||
| chr5:180634938
|
A | G | 4 | a0001c0001t0002g0216a0002c0002t0004g0033a0002c0003t0001g0321others(1): Show | 4 | HG02486.hp2 NA19079.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3160T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634938 | ||||||
| chr5:180634941
|
G | C | 4 | a0001c0001t0001g0069a0001c0001t0001g0092a0002c0004t0031g0279others(1): Show | 4 | HG00558.hp1 HG02165.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3163C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634941 | ||||||
| chr5:180634942
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3164T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634942 | ||||||
| chr5:180634943
|
TGCATGGA others(1): Show |
T | 7 | a0001c0001t0001g0118a0001c0001t0006g0343a0002c0002t0001g0072others(4): Show | 7 | HG02080.hp1 HG02717.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3173_59-3166del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634943 | ||||||
| chr5:180634945
|
C | CATGG | 37 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0075others(34): Show | 37 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-3171_59-3168dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634945 | ||||||
| chr5:180634945
|
C | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0002g0216others(5): Show | 8 | HG00558.hp1 HG02165.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3167G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634945 | ||||||
| chr5:180634945
|
CATGGAGG others(101): Show |
C | 3 | a0001c0001t0002g0310a0001c0001t0002g0311a0002c0011t0014g0166 | 3 | HG02735.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59-3275_59-3168del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634945 | ||||||
| chr5:180634945
|
CATGGAGG others(209): Show |
C | 1 | a0002c0002t0001g0337 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.59-3383_59-3168del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634945 | ||||||
| chr5:180634946
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3168T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634946 | ||||||
| chr5:180634951
|
G | C | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3173C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634951 | ||||||
| chr5:180634951
|
G | T | 45 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(42): Show | 45 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.59-3173C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634951 | ||||||
| chr5:180634953
|
GAAGT | G | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3179_59-3176del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634953 | ||||||
| chr5:180634957
|
T | TATGGGTG others(1): Show |
5 | a0001c0001t0020g0361a0002c0002t0001g0205a0002c0002t0001g0351others(2): Show | 5 | HG00609.hp2 HG00738.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3187_59-3180dup others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634957 | ||||||
| chr5:180634962
|
G | A | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3184C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634962 | ||||||
| chr5:180634963
|
T | A | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3185A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634963 | ||||||
| chr5:180634965
|
G | T | 5 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253others(2): Show | 5 | HG02040.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3187C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634965 | ||||||
| chr5:180634966
|
A | G | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3188T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634966 | ||||||
| chr5:180634967
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.59-3189A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634967 | ||||||
| chr5:180634970
|
G | GTGGATGG others(21): Show |
1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3193_59-3192ins others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634970 | ||||||
| chr5:180634970
|
G | GTGGGTGG others(223): Show |
1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3193_59-3192ins others(230): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634970 | ||||||
| chr5:180634973
|
G | A | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3195C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634973 | ||||||
| chr5:180634974
|
G | A | 29 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(26): Show | 29 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-3196C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634974 | ||||||
| chr5:180634974
|
G | GTGGGTGG others(73): Show |
1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3197_59-3196ins others(80): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634974 | ||||||
| chr5:180634974
|
G | GTGGGTGG others(153): Show |
1 | a0001c0001t0002g0216 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.59-3197_59-3196ins others(160): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634974 | ||||||
| chr5:180634974
|
G | GTGGGTGG others(205): Show |
1 | a0002c0008t0004g0296 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.59-3197_59-3196ins others(212): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634974 | ||||||
| chr5:180634977
|
G | GATGGATG others(133): Show |
1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3200_59-3199ins others(140): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634977 | ||||||
| chr5:180634978
|
G | A | 2 | a0002c0002t0001g0089a0002c0002t0001g0254 | 2 | HG02015.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.59-3200C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634978 | ||||||
| chr5:180634978
|
GTGGGTGG others(9): Show |
G | 8 | a0001c0001t0001g0113a0001c0001t0002g0229a0001c0043t0002g0230others(5): Show | 8 | HG01981.hp2 HG02055.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3216_59-3201del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634978 | ||||||
| chr5:180634981
|
GGTGGCTG others(1): Show |
G | 63 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0091others(60): Show | 64 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-3211_59-3204del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634981 | ||||||
| chr5:180634981
|
GGTGGCTG others(13): Show |
G | 8 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0365others(5): Show | 8 | HG00642.hp2 HG03491.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3223_59-3204del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634981 | ||||||
| chr5:180634982
|
G | A | 2 | a0001c0001t0002g0275a0002c0002t0004g0033 | 2 | NA18980.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3204C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634982 | ||||||
| chr5:180634982
|
GTGGCTGA others(5): Show |
G | 2 | a0001c0001t0003g0227a0002c0003t0003g0190 | 2 | HG02040.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.59-3216_59-3205del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634982 | ||||||
| chr5:180634983
|
TGGCTGAG others(1): Show |
T | 14 | a0001c0001t0001g0215a0001c0001t0001g0356a0001c0001t0002g0177others(11): Show | 14 | HG00639.hp1 HG00673.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3213_59-3206del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634983 | ||||||
| chr5:180634985
|
G | C | 1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-3207C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634985 | ||||||
| chr5:180634985
|
G | GATGGATG others(5): Show |
1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3208_59-3207ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634985 | ||||||
| chr5:180634985
|
GCTGA | G | 3 | a0002c0002t0001g0011a0005c0018t0013g0167a0030c0050t0001g0112 | 3 | HG01109.hp1 HG02257.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.59-3211_59-3208del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634985 | ||||||
| chr5:180634986
|
C | A | 3 | a0001c0001t0002g0275a0002c0002t0001g0254a0002c0002t0004g0033 | 3 | NA18612.hp1 NA18980.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3208G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634986 | ||||||
| chr5:180634986
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(224): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.59-3208G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634986 | ||||||
| chr5:180634989
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(226): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.59-3211T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634989 | ||||||
| chr5:180634990
|
G | A | 1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-3212C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634990 | ||||||
| chr5:180634991
|
A | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(224): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.59-3213T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634991 | ||||||
| chr5:180634994
|
A | ATGGAAGT others(5): Show |
1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-3217_59-3216ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634994 | ||||||
| chr5:180634994
|
A | G | 2 | a0002c0002t0001g0011a0002c0002t0001g0089 | 2 | HG01109.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.59-3216T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634994 | ||||||
| chr5:180634995
|
T | C | 3 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253 | 3 | NA18966.hp1 NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3217A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634995 | ||||||
| chr5:180634998
|
A | G | 1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3220T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634998 | ||||||
| chr5:180634999
|
T | C | 2 | a0001c0001t0003g0227a0002c0003t0003g0190 | 2 | HG02040.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.59-3221A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180634999 | ||||||
| chr5:180635001
|
C | G | 17 | a0001c0001t0001g0215a0001c0001t0002g0082a0001c0001t0002g0123others(14): Show | 17 | HG01891.hp2 HG01952.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-3223G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635001 | ||||||
| chr5:180635001
|
CATGG | C | 19 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0001g0356others(16): Show | 19 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.59-3227_59-3224del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635001 | ||||||
| chr5:180635002
|
A | G | 2 | a0001c0001t0002g0275a0002c0002t0004g0033 | 2 | NA18980.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3224T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635002 | ||||||
| chr5:180635005
|
G | C | 2 | a0001c0001t0001g0118a0002c0002t0001g0089 | 2 | HG02015.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.59-3227C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635005 | ||||||
| chr5:180635006
|
A | ATGGATGG others(21): Show |
1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3229_59-3228ins others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635006 | ||||||
| chr5:180635006
|
A | G | 2 | a0001c0001t0002g0275a0002c0002t0004g0033 | 2 | NA18980.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3228T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635006 | ||||||
| chr5:180635007
|
T | A | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3229A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635007 | ||||||
| chr5:180635007
|
TGGAC | T | 8 | a0004c0007t0001g0010a0004c0007t0001g0015a0004c0007t0001g0017others(5): Show | 9 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3233_59-3230del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635007 | ||||||
| chr5:180635007
|
TGGACG | T | 3 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0253 | 3 | NA18966.hp1 NA18969.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3234_59-3230del others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635007 | ||||||
| chr5:180635009
|
G | T | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3231C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635009 | ||||||
| chr5:180635011
|
C | G | 22 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0001g0100others(19): Show | 22 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-3233G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635011 | ||||||
| chr5:180635011
|
C | T | 101 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(98): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.59-3233G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635011 | ||||||
| chr5:180635014
|
A | G | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3236T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635014 | ||||||
| chr5:180635015
|
A | T | 11 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(8): Show | 11 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3237T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635015 | ||||||
| chr5:180635017
|
T | G | 11 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(8): Show | 11 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3239A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635017 | ||||||
| chr5:180635017
|
TATGGGTG others(1): Show |
T | 7 | a0001c0001t0001g0215a0001c0001t0002g0177a0001c0001t0002g0229others(4): Show | 7 | HG02040.hp1 HG02055.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3247_59-3240del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635017 | ||||||
| chr5:180635022
|
G | A | 2 | a0001c0001t0002g0275a0002c0002t0004g0033 | 2 | NA18980.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3244C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635022 | ||||||
| chr5:180635025
|
G | GATGGGTG others(25): Show |
1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3248_59-3247ins others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635025 | ||||||
| chr5:180635026
|
A | G | 9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3248T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635026 | ||||||
| chr5:180635026
|
ATGGGTGG others(5): Show |
A | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0295others(2): Show | 5 | HG01515.hp2 HG02129.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3260_59-3249del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635026 | ||||||
| chr5:180635030
|
G | GTGGGTGG others(33): Show |
1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3253_59-3252ins others(40): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635030 | ||||||
| chr5:180635030
|
GTGGA | G | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0365others(6): Show | 9 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3256_59-3253del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635030 | ||||||
| chr5:180635033
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(107): Show | 117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.59-3255C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635033 | ||||||
| chr5:180635033
|
G | GGTGGATG others(17): Show |
9 | a0001c0001t0002g0082a0001c0001t0002g0123a0001c0001t0002g0124others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3256_59-3255ins others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635033 | ||||||
| chr5:180635033
|
G | GGTGGGTG others(165): Show |
1 | a0001c0001t0002g0216 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.59-3256_59-3255ins others(172): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635033 | ||||||
| chr5:180635034
|
A | G | 45 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(42): Show | 45 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.59-3256T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635034 | ||||||
| chr5:180635039
|
T | A | 1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3261A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635039 | ||||||
| chr5:180635042
|
G | A | 7 | a0001c0001t0002g0312a0001c0001t0003g0338a0002c0002t0001g0072others(4): Show | 7 | HG00423.hp1 HG02723.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3264C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635042 | ||||||
| chr5:180635043
|
T | A | 12 | a0001c0001t0001g0356a0001c0001t0006g0343a0002c0002t0001g0011others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3265A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635043 | ||||||
| chr5:180635043
|
TGGGTGGG others(29): Show |
T | 6 | a0001c0001t0001g0070a0002c0002t0001g0339a0002c0003t0003g0095others(3): Show | 6 | HG00673.hp2 HG02083.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3301_59-3266del others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635043 | ||||||
| chr5:180635046
|
G | A | 31 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(28): Show | 31 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-3268C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635046 | ||||||
| chr5:180635050
|
G | A | 60 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(57): Show | 60 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.59-3272C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635050 | ||||||
| chr5:180635050
|
G | GTGGGTGG others(233): Show |
1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3273_59-3272ins others(240): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635050 | ||||||
| chr5:180635051
|
T | A | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-3273A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635051 | ||||||
| chr5:180635051
|
T | C | 4 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0295others(1): Show | 4 | HG02129.hp1 NA18948.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3273A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635051 | ||||||
| chr5:180635051
|
TGGATGGA others(61): Show |
T | 4 | a0002c0002t0001g0002a0002c0002t0001g0353a0002c0002t0001g0355others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3341_59-3274del others(68): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635051 | ||||||
| chr5:180635053
|
G | C | 27 | a0001c0001t0001g0128a0001c0001t0001g0215a0001c0001t0001g0356others(24): Show | 27 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-3275C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635053 | ||||||
| chr5:180635053
|
G | GATGGATG others(1): Show |
5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0092others(2): Show | 5 | HG02165.hp2 NA18970.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3276_59-3275ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635053 | ||||||
| chr5:180635053
|
G | GGTGGGTG others(9): Show |
1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3276_59-3275ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635053 | ||||||
| chr5:180635054
|
A | G | 1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3276T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635054 | ||||||
| chr5:180635054
|
ATGGATGG others(25): Show |
A | 2 | a0001c0001t0001g0100a0002c0002t0004g0014 | 2 | HG00423.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.59-3308_59-3277del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635054 | ||||||
| chr5:180635054
|
ATGGATGG others(97): Show |
A | 1 | a0006c0014t0009g0301 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-3380_59-3277del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635054 | ||||||
| chr5:180635054
|
ATGGATGG others(341): Show |
A | 1 | a0002c0004t0031g0279 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.59-3624_59-3277del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635054 | ||||||
| chr5:180635055
|
T | A | 7 | a0001c0001t0002g0312a0001c0001t0003g0338a0002c0002t0001g0072others(4): Show | 7 | HG00423.hp1 HG02723.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3277A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635055 | ||||||
| chr5:180635056
|
G | A | 1 | a0001c0001t0006g0343 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.59-3278C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635056 | ||||||
| chr5:180635057
|
G | C | 6 | a0001c0001t0001g0365a0001c0001t0015g0332a0002c0002t0001g0027others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3279C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGC | 42 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0091others(39): Show | 42 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.59-3280_59-3279ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(329): Show |
1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(329): Show |
1 | a0002c0008t0004g0296 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(329): Show |
17 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(14): Show | 17 | HG01070.hp1 HG01123.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-3280_59-3279ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(165): Show |
1 | a0002c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(172): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(481): Show |
2 | a0001c0001t0010g0368a0002c0003t0001g0370 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.59-3280_59-3279ins others(488): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(545): Show |
1 | a0001c0001t0002g0372 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(552): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(1181): Show |
1 | a0001c0001t0002g0371 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(1188): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(1281): Show |
3 | a0002c0003t0001g0317a0002c0012t0021g0174a0006c0033t0009g0376 | 3 | HG02809.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-3280_59-3279ins others(1288): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | GATGGATG others(1033): Show |
1 | a0002c0003t0007g0373 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-3280_59-3279ins others(1040): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635057
|
G | T | 7 | a0001c0001t0002g0312a0001c0001t0003g0338a0002c0002t0001g0072others(4): Show | 7 | HG00423.hp1 HG02723.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3279C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635057 | ||||||
| chr5:180635058
|
A | G | 1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3280T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635058 | ||||||
| chr5:180635058
|
ATGGATGG others(93): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-3380_59-3281del others(100): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635058 | ||||||
| chr5:180635059
|
T | A | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0032t0026g0333others(2): Show | 5 | HG00733.hp2 HG01074.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3281A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635059 | ||||||
| chr5:180635059
|
T | G | 6 | a0001c0001t0006g0344a0002c0002t0001g0211a0002c0002t0001g0346others(3): Show | 6 | HG00642.hp2 HG03453.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3281A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635059 | ||||||
| chr5:180635061
|
G | C | 3 | a0001c0001t0001g0071a0002c0003t0003g0143a0023c0036t0001g0110 | 3 | HG02155.hp1 NA18951.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.59-3283C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635061 | ||||||
| chr5:180635061
|
G | GAAGT | 6 | a0001c0001t0006g0344a0002c0002t0001g0211a0002c0002t0001g0346others(3): Show | 6 | HG00642.hp2 HG03453.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3284_59-3283ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635061 | ||||||
| chr5:180635061
|
G | T | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0032t0026g0333others(2): Show | 5 | HG00733.hp2 HG01074.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3283C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635061 | ||||||
| chr5:180635062
|
A | G | 7 | a0001c0001t0002g0312a0001c0001t0003g0338a0002c0002t0001g0072others(4): Show | 7 | HG00423.hp1 HG02723.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3284T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635062 | ||||||
| chr5:180635063
|
T | C | 3 | a0001c0001t0001g0092a0002c0002t0001g0349a0002c0004t0033g0090 | 3 | HG02165.hp2 HG02683.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.59-3285A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635063 | ||||||
| chr5:180635063
|
T | G | 47 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.59-3285A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635063 | ||||||
| chr5:180635063
|
TG | T | 4 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0295others(1): Show | 4 | HG02129.hp1 NA18948.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3286delC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635063 | ||||||
| chr5:180635065
|
GAAGT | G | 8 | a0001c0001t0002g0312a0001c0001t0003g0338a0002c0002t0001g0072others(5): Show | 8 | HG00423.hp1 HG02155.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3291_59-3288del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635065 | ||||||
| chr5:180635066
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0006g0344others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3288T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635066 | ||||||
| chr5:180635066
|
AAGTATGG others(800): Show |
A | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-4095_59-3289del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635066 | ||||||
| chr5:180635067
|
A | T | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0006g0344others(9): Show | 12 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3289T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635067 | ||||||
| chr5:180635069
|
T | C | 1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3291A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635069 | ||||||
| chr5:180635069
|
T | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0006g0344others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3291A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635069 | ||||||
| chr5:180635069
|
T | TATGGGTG others(1): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0360others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3299_59-3292dup others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635069 | ||||||
| chr5:180635069
|
T | TATGGGTG others(9): Show |
1 | a0002c0002t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-3292_59-3291ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635069 | ||||||
| chr5:180635070
|
A | ATGGATGG others(25): Show |
1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3293_59-3292ins others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635070 | ||||||
| chr5:180635070
|
A | ATGGGTGG others(5): Show |
1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3293_59-3292ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635070 | ||||||
| chr5:180635070
|
A | ATGGGTGG others(9): Show |
3 | a0001c0001t0001g0092a0002c0002t0001g0061a0002c0004t0033g0090 | 3 | HG02165.hp2 NA18980.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.59-3293_59-3292ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635070 | ||||||
| chr5:180635070
|
ATGGGTGG others(5): Show |
A | 4 | a0001c0001t0001g0356a0001c0001t0006g0343a0002c0003t0002g0325others(1): Show | 4 | HG02698.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3304_59-3293del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635070 | ||||||
| chr5:180635074
|
G | A | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-3296C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635074 | ||||||
| chr5:180635074
|
G | GTGGA | 41 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0091others(38): Show | 41 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.59-3297_59-3296ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635074 | ||||||
| chr5:180635075
|
T | C | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-3297A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635075 | ||||||
| chr5:180635075
|
T | G | 1 | a0001c0001t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.59-3297A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635075 | ||||||
| chr5:180635076
|
G | GGATGGGT others(76): Show |
3 | a0001c0001t0001g0330a0012c0017t0001g0328a0012c0017t0001g0329 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-3299_59-3298ins others(83): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635076 | ||||||
| chr5:180635076
|
G | GGATGGGT others(40): Show |
1 | a0001c0001t0001g0367 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.59-3299_59-3298ins others(47): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635076 | ||||||
| chr5:180635076
|
G | GGATGGGT others(316): Show |
1 | a0002c0003t0002g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-3299_59-3298ins others(323): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635076 | ||||||
| chr5:180635076
|
G | GGATGGGT others(76): Show |
117 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.59-3299_59-3298ins others(83): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635076 | ||||||
| chr5:180635076
|
G | GGATGGGT others(76): Show |
25 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(22): Show | 25 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-3299_59-3298ins others(83): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635076 | ||||||
| chr5:180635077
|
GGAGGGTG others(25): Show |
G | 3 | a0001c0001t0012g0357a0002c0003t0006g0334a0002c0003t0006g0335 | 3 | HG00280.hp2 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-3331_59-3300del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635077 | ||||||
| chr5:180635077
|
GGAGGGTG others(133): Show |
G | 1 | a0002c0002t0001g0354 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.59-3439_59-3300del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635077 | ||||||
| chr5:180635077
|
GGAGGGTG others(173): Show |
G | 5 | a0002c0002t0001g0205a0002c0002t0001g0351a0002c0002t0001g0352others(2): Show | 5 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3479_59-3300del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635077 | ||||||
| chr5:180635077
|
GGAGGGTG others(724): Show |
G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4030_59-3300del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635077 | ||||||
| chr5:180635078
|
G | A | 51 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0001g0128others(48): Show | 51 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.59-3300C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635078 | ||||||
| chr5:180635079
|
A | AT | 149 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.59-3302_59-3301ins others(1): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635079 | ||||||
| chr5:180635079
|
A | G | 1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3301T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635079 | ||||||
| chr5:180635079
|
A | T | 152 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.59-3301T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635079 | ||||||
| chr5:180635081
|
G | T | 2 | a0001c0001t0001g0071a0002c0003t0003g0143 | 2 | HG02155.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.59-3303C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635081 | ||||||
| chr5:180635082
|
G | A | 2 | a0001c0001t0001g0071a0002c0003t0003g0143 | 2 | HG02155.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.59-3304C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635082 | ||||||
| chr5:180635083
|
T | A | 1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3305A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635083 | ||||||
| chr5:180635084
|
G | GGGTGGGG others(77): Show |
1 | a0007c0010t0015g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.59-3307_59-3306ins others(84): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635084 | ||||||
| chr5:180635085
|
GGTGGATG others(85): Show |
G | 2 | a0002c0003t0007g0314a0002c0003t0007g0315 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.59-3399_59-3308del others(92): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635085 | ||||||
| chr5:180635086
|
G | A | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3308C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635086 | ||||||
| chr5:180635086
|
G | GAGGA | 6 | a0001c0001t0006g0344a0002c0002t0001g0211a0002c0002t0001g0346others(3): Show | 6 | HG00642.hp2 HG03453.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3309_59-3308ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635086 | ||||||
| chr5:180635086
|
GTGGATGG others(17): Show |
G | 7 | a0001c0001t0001g0113a0001c0001t0002g0116a0001c0001t0005g0117others(4): Show | 7 | HG01981.hp2 HG02040.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3332_59-3309del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635086 | ||||||
| chr5:180635086
|
GTGGATGG others(884): Show |
G | 1 | a0002c0004t0005g0278 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.59-4199_59-3309del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635086 | ||||||
| chr5:180635087
|
TGGATGGA others(301): Show |
T | 1 | a0002c0002t0001g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.59-3617_59-3310del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635087 | ||||||
| chr5:180635088
|
G | GGATGGAT others(329): Show |
1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3311_59-3310ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635088 | ||||||
| chr5:180635090
|
A | G | 32 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(29): Show | 32 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-3312T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635090 | ||||||
| chr5:180635091
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0002g0275a0001c0001t0003g0227others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3313A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635091 | ||||||
| chr5:180635091
|
TGGATGGA others(53): Show |
T | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-3373_59-3314del others(60): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635091 | ||||||
| chr5:180635093
|
G | C | 38 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0100others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.59-3315C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635093 | ||||||
| chr5:180635094
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0071others(23): Show | 26 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3316T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635094 | ||||||
| chr5:180635095
|
T | A | 2 | a0001c0001t0001g0365a0002c0002t0001g0027 | 2 | HG00099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.59-3317A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635095 | ||||||
| chr5:180635097
|
G | C | 29 | a0001c0001t0001g0070a0001c0001t0001g0092a0001c0001t0001g0129others(26): Show | 29 | HG00423.hp1 HG00673.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3319C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635097 | ||||||
| chr5:180635097
|
GATGGATG others(5): Show |
G | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-3331_59-3320del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635097 | ||||||
| chr5:180635098
|
A | G | 13 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0106others(10): Show | 13 | HG00735.hp1 HG02027.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3320T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635098 | ||||||
| chr5:180635102
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0356a0001c0001t0006g0343others(2): Show | 5 | HG02698.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3324T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635102 | ||||||
| chr5:180635102
|
ATGGAAGT others(49): Show |
A | 2 | a0001c0001t0002g0253a0002c0002t0001g0027 | 2 | HG00099.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.59-3380_59-3325del others(56): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635102 | ||||||
| chr5:180635103
|
T | C | 3 | a0001c0001t0001g0100a0002c0002t0001g0061a0002c0002t0004g0014 | 3 | HG00423.hp2 HG01928.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.59-3325A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635103 | ||||||
| chr5:180635103
|
T | G | 23 | a0001c0001t0001g0070a0001c0001t0001g0092a0001c0001t0001g0129others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-3325A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635103 | ||||||
| chr5:180635103
|
TG | T | 5 | a0001c0001t0002g0229a0001c0001t0002g0275a0001c0001t0003g0227others(2): Show | 5 | HG02040.hp1 HG02055.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3326delC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635103 | ||||||
| chr5:180635105
|
G | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0365others(4): Show | 7 | HG00323.hp2 HG02080.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3327C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635105 | ||||||
| chr5:180635105
|
GAAGT | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0356a0001c0001t0006g0343others(2): Show | 5 | HG02698.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3331_59-3328del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635105 | ||||||
| chr5:180635106
|
A | G | 1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3328T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635106 | ||||||
| chr5:180635106
|
AAGTATGG others(9): Show |
A | 1 | a0001c0001t0001g0365 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59-3344_59-3329del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635106 | ||||||
| chr5:180635106
|
AAGTATGG others(13): Show |
A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3348_59-3329del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635106 | ||||||
| chr5:180635107
|
A | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(14): Show | 17 | HG00323.hp2 HG00735.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-3329T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635107 | ||||||
| chr5:180635109
|
T | C | 11 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0002g0066others(8): Show | 11 | HG00735.hp1 HG02027.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3331A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635109 | ||||||
| chr5:180635109
|
T | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0012g0358others(3): Show | 6 | HG00323.hp2 HG02080.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3331A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635109 | ||||||
| chr5:180635110
|
A | G | 6 | a0001c0001t0001g0071a0001c0001t0001g0356a0001c0001t0006g0343others(3): Show | 6 | HG02155.hp1 HG02698.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3332T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635110 | ||||||
| chr5:180635114
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(13): Show | 16 | HG00323.hp2 HG00735.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-3336C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635114 | ||||||
| chr5:180635115
|
T | C | 3 | a0001c0001t0012g0358a0002c0003t0003g0077a0002c0003t0003g0102 | 3 | HG00323.hp2 HG02080.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.59-3337A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635115 | ||||||
| chr5:180635117
|
GAGGGGTG others(93): Show |
G | 1 | a0002c0002t0001g0345 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.59-3439_59-3340del others(100): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635117 | ||||||
| chr5:180635118
|
A | ATGGGTGG others(5): Show |
1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3341_59-3340ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635118 | ||||||
| chr5:180635118
|
A | ATGGGTGG others(9): Show |
6 | a0002c0002t0001g0097a0002c0002t0003g0246a0002c0002t0003g0247others(3): Show | 6 | NA18950.hp1 NA18954.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3341_59-3340ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635118 | ||||||
| chr5:180635118
|
A | G | 23 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0001g0356others(20): Show | 23 | HG00280.hp2 HG01981.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-3340T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635118 | ||||||
| chr5:180635118
|
AGGGG | A | 12 | a0001c0001t0001g0111a0001c0001t0024g0105a0001c0009t0002g0114others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3344_59-3341del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635118 | ||||||
| chr5:180635119
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0012g0358others(2): Show | 5 | HG00323.hp2 HG02080.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3341C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635119 | ||||||
| chr5:180635119
|
G | C | 11 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0002g0066others(8): Show | 11 | HG00735.hp1 HG02027.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3341C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635119 | ||||||
| chr5:180635119
|
G | GGGGTGGG others(48): Show |
1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-3342_59-3341ins others(55): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635119 | ||||||
| chr5:180635119
|
G | T | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(86): Show | 89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.59-3341C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635119 | ||||||
| chr5:180635121
|
G | GAAGT | 11 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0002g0066others(8): Show | 11 | HG00735.hp1 HG02027.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3344_59-3343ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635121 | ||||||
| chr5:180635121
|
G | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0012g0358others(2): Show | 5 | HG00323.hp2 HG02080.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3343C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635121 | ||||||
| chr5:180635122
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(13): Show | 16 | HG00323.hp2 HG00735.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-3344C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635122 | ||||||
| chr5:180635125
|
GGTGGATG others(5): Show |
G | 3 | a0001c0001t0001g0069a0001c0001t0004g0131a0002c0002t0004g0096 | 3 | HG00558.hp1 HG02074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.59-3359_59-3348del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635125 | ||||||
| chr5:180635126
|
G | A | 10 | a0001c0001t0001g0365a0001c0001t0004g0087a0001c0001t0004g0142others(7): Show | 10 | HG00642.hp2 HG02027.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3348C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635126 | ||||||
| chr5:180635126
|
GTGGATGG others(5): Show |
G | 2 | a0001c0001t0001g0100a0002c0002t0004g0014 | 2 | HG00423.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.59-3360_59-3349del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635126 | ||||||
| chr5:180635127
|
T | A | 9 | a0002c0002t0001g0097a0002c0002t0003g0246a0002c0002t0003g0247others(6): Show | 9 | HG02155.hp1 HG03927.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3349A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635127 | ||||||
| chr5:180635127
|
T | TGGGTGGG others(1): Show |
5 | a0001c0001t0003g0338a0002c0002t0001g0072a0002c0003t0003g0134others(2): Show | 5 | HG00423.hp1 NA18944.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3350_59-3349ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635127 | ||||||
| chr5:180635130
|
A | G | 45 | a0001c0001t0001g0070a0001c0001t0001g0092a0001c0001t0001g0128others(42): Show | 45 | HG00642.hp2 HG00673.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.59-3352T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635130 | ||||||
| chr5:180635132
|
GGATGCAT | G | 5 | a0001c0001t0001g0128a0001c0001t0002g0312a0001c0032t0026g0333others(2): Show | 5 | HG02723.hp1 HG02965.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3361_59-3355del others(7): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635132 | ||||||
| chr5:180635133
|
G | C | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3355C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635133 | ||||||
| chr5:180635133
|
GATGC | G | 13 | a0001c0001t0001g0111a0001c0001t0012g0358a0001c0001t0024g0105others(10): Show | 13 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3359_59-3356del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635133 | ||||||
| chr5:180635134
|
A | G | 40 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(37): Show | 40 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.59-3356T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635134 | ||||||
| chr5:180635135
|
T | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0365others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3357A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635135 | ||||||
| chr5:180635137
|
C | G | 51 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(48): Show | 51 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.59-3359G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635137 | ||||||
| chr5:180635137
|
C | T | 1 | a0001c0001t0001g0365 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59-3359G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635137 | ||||||
| chr5:180635138
|
A | G | 40 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.59-3360T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635138 | ||||||
| chr5:180635139
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3361A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635139 | ||||||
| chr5:180635141
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3363C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635141 | ||||||
| chr5:180635141
|
G | T | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3363C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635141 | ||||||
| chr5:180635142
|
A | AAGTATGG others(1): Show |
5 | a0001c0001t0001g0360a0001c0006t0002g0155a0001c0047t0001g0173others(2): Show | 5 | HG02572.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3365_59-3364ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635142 | ||||||
| chr5:180635142
|
A | AAGTATGG others(129): Show |
1 | a0001c0001t0004g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.59-3365_59-3364ins others(136): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635142 | ||||||
| chr5:180635142
|
A | G | 46 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(43): Show | 46 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.59-3364T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635142 | ||||||
| chr5:180635142
|
AT | A | 5 | a0001c0001t0001g0128a0001c0001t0002g0312a0001c0032t0026g0333others(2): Show | 5 | HG02723.hp1 HG02965.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3365delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635142 | ||||||
| chr5:180635142
|
ATGGATGG others(9): Show |
A | 4 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0295others(1): Show | 4 | HG02129.hp1 NA18948.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3380_59-3365del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635142 | ||||||
| chr5:180635143
|
T | G | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3365A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635143 | ||||||
| chr5:180635145
|
G | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0215others(7): Show | 10 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-3367C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635145 | ||||||
| chr5:180635146
|
A | AAGTATGG others(1): Show |
3 | a0001c0001t0006g0209a0024c0046t0009g0327a0027c0042t0028g0379 | 3 | HG03195.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.59-3369_59-3368ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635146 | ||||||
| chr5:180635146
|
A | G | 41 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(38): Show | 41 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.59-3368T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635146 | ||||||
| chr5:180635147
|
T | A | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3369A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635147 | ||||||
| chr5:180635147
|
T | C | 17 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0001g0356others(14): Show | 18 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3369A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635147 | ||||||
| chr5:180635147
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3369A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635147 | ||||||
| chr5:180635149
|
G | T | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3371C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635149 | ||||||
| chr5:180635150
|
A | AAGTATGG others(9): Show |
1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3373_59-3372ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635150 | ||||||
| chr5:180635150
|
A | G | 47 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.59-3372T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635150 | ||||||
| chr5:180635150
|
AAGGGTGG others(1): Show |
A | 18 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(15): Show | 18 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3380_59-3373del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635150 | ||||||
| chr5:180635151
|
A | AGTATGGG others(297): Show |
1 | a0001c0001t0001g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(304): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(5): Show |
1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(9): Show |
1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(97): Show |
1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(104): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(305): Show |
1 | a0001c0001t0002g0216 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(312): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(93): Show |
20 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0217others(17): Show | 20 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-3374_59-3373ins others(100): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(53): Show |
37 | a0001c0001t0001g0062a0001c0001t0001g0224a0001c0001t0001g0225others(34): Show | 37 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.59-3374_59-3373ins others(60): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(57): Show |
125 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(122): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.59-3374_59-3373ins others(64): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(229): Show |
1 | a0002c0002t0001g0016 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(236): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(85): Show |
3 | a0002c0002t0001g0097a0002c0002t0004g0080a0002c0002t0004g0098 | 3 | NA18950.hp1 NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.59-3374_59-3373ins others(92): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | AGTATGGG others(52): Show |
1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3374_59-3373ins others(59): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | G | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3373T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635151
|
A | T | 41 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(38): Show | 41 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.59-3373T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635151 | ||||||
| chr5:180635153
|
G | C | 3 | a0001c0001t0004g0078a0001c0001t0004g0087a0002c0002t0001g0061 | 3 | NA18975.hp2 NA18992.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.59-3375C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635153 | ||||||
| chr5:180635153
|
G | T | 45 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0092others(42): Show | 46 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.59-3375C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635153 | ||||||
| chr5:180635154
|
G | A | 67 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(64): Show | 68 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.59-3376C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635154 | ||||||
| chr5:180635158
|
G | A | 75 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(72): Show | 75 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.59-3380C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635158 | ||||||
| chr5:180635158
|
G | GTGGGTGG others(5): Show |
1 | a0024c0046t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-3381_59-3380ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635158 | ||||||
| chr5:180635159
|
T | C | 1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3381A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635159 | ||||||
| chr5:180635159
|
T | G | 6 | a0001c0001t0001g0215a0001c0001t0002g0310a0001c0001t0002g0311others(3): Show | 6 | HG01109.hp1 HG02735.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3381A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635159 | ||||||
| chr5:180635161
|
G | A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3383C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | C | 33 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0118others(30): Show | 33 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.59-3383C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | GAGGGGTG others(257): Show |
2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59-3384_59-3383ins others(264): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | GATGGGTG others(49): Show |
1 | a0002c0003t0001g0375 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.59-3384_59-3383ins others(56): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | GATGGGTG others(21): Show |
2 | a0001c0001t0002g0275a0001c0001t0003g0227 | 2 | NA18953.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.59-3384_59-3383ins others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | GATGGGTG others(137): Show |
1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-3384_59-3383ins others(144): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
G | GATGGGTG others(141): Show |
2 | a0002c0003t0001g0243a0004c0007t0001g0015 | 2 | HG01496.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.59-3384_59-3383ins others(148): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635161
|
GATGGATG others(9): Show |
G | 2 | a0002c0003t0006g0334a0002c0003t0006g0335 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-3399_59-3384del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635161 | ||||||
| chr5:180635162
|
A | G | 4 | a0001c0001t0002g0177a0001c0001t0002g0273a0002c0002t0001g0089others(1): Show | 4 | HG02015.hp2 NA18969.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3384T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635162 | ||||||
| chr5:180635163
|
T | A | 6 | a0001c0001t0001g0215a0001c0001t0002g0310a0001c0001t0002g0311others(3): Show | 6 | HG01109.hp1 HG02735.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3385A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635163 | ||||||
| chr5:180635163
|
T | C | 2 | a0001c0001t0004g0078a0002c0002t0001g0061 | 2 | NA18992.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.59-3385A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635163 | ||||||
| chr5:180635165
|
G | C | 26 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(23): Show | 26 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3387C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635165 | ||||||
| chr5:180635165
|
G | T | 6 | a0001c0001t0001g0215a0001c0001t0002g0310a0001c0001t0002g0311others(3): Show | 6 | HG01109.hp1 HG02735.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3387C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635165 | ||||||
| chr5:180635165
|
GATGGATG others(5): Show |
G | 14 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0001g0356others(11): Show | 15 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3399_59-3388del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635165 | ||||||
| chr5:180635166
|
A | G | 25 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0002g0116others(22): Show | 25 | HG00423.hp1 HG00673.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.59-3388T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635166 | ||||||
| chr5:180635167
|
T | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0004g0078others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3389A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635167 | ||||||
| chr5:180635169
|
G | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0004g0078others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3391C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635169 | ||||||
| chr5:180635169
|
GATGGAAG others(1): Show |
G | 15 | a0001c0001t0001g0092a0001c0001t0002g0116a0001c0001t0003g0338others(12): Show | 15 | HG00423.hp1 HG00673.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3399_59-3392del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635169 | ||||||
| chr5:180635170
|
A | G | 11 | a0001c0001t0001g0215a0001c0001t0002g0310a0001c0001t0002g0311others(8): Show | 11 | HG01109.hp1 HG02015.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3392T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635170 | ||||||
| chr5:180635171
|
T | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0118a0001c0001t0006g0344others(6): Show | 9 | HG00642.hp2 HG02109.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3393A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635171 | ||||||
| chr5:180635171
|
T | G | 25 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-3393A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635171 | ||||||
| chr5:180635173
|
GAAGT | G | 4 | a0001c0001t0001g0075a0002c0002t0003g0246a0002c0002t0003g0247others(1): Show | 4 | HG00741.hp2 NA18954.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3399_59-3396del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635173 | ||||||
| chr5:180635173
|
GAAGTATG others(37): Show |
G | 2 | a0002c0002t0001g0339a0002c0003t0003g0132 | 2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.59-3439_59-3396del others(44): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635173 | ||||||
| chr5:180635174
|
A | G | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0004g0078others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3396T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635174 | ||||||
| chr5:180635175
|
A | T | 14 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0215others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3397T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635175 | ||||||
| chr5:180635177
|
T | C | 1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3399A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635177 | ||||||
| chr5:180635177
|
T | G | 14 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0215others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3399A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635177 | ||||||
| chr5:180635178
|
A | G | 30 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0113others(27): Show | 31 | HG00280.hp2 HG00741.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.59-3400T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635178 | ||||||
| chr5:180635182
|
G | A | 2 | a0002c0002t0001g0089a0002c0002t0001g0202 | 2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3404C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635182 | ||||||
| chr5:180635185
|
G | C | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3407C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635185 | ||||||
| chr5:180635186
|
A | ATGGGTGG others(5): Show |
1 | a0001c0001t0006g0344 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.59-3420_59-3409dup others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635186 | ||||||
| chr5:180635186
|
A | G | 49 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0092others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.59-3408T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635186 | ||||||
| chr5:180635187
|
T | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3409A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635187 | ||||||
| chr5:180635190
|
G | A | 2 | a0002c0002t0001g0089a0002c0002t0001g0202 | 2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3412C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635190 | ||||||
| chr5:180635191
|
T | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0215a0001c0001t0002g0310others(4): Show | 7 | HG00741.hp2 HG01109.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3413A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635191 | ||||||
| chr5:180635193
|
G | T | 1 | a0002c0002t0001g0202 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.59-3415C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635193 | ||||||
| chr5:180635193
|
GGTGGGTG others(17): Show |
G | 3 | a0001c0032t0026g0333a0002c0002t0001g0027a0002c0003t0005g0103 | 3 | HG00099.hp1 HG02965.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.59-3439_59-3416del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635193 | ||||||
| chr5:180635194
|
G | A | 15 | a0001c0001t0001g0075a0001c0001t0001g0215a0001c0001t0002g0229others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3416C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635194 | ||||||
| chr5:180635194
|
GTGGGTGG others(17): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-3440_59-3417del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635194 | ||||||
| chr5:180635198
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(233): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.59-3420C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635198 | ||||||
| chr5:180635198
|
GTGGATGG others(13): Show |
G | 13 | a0001c0001t0001g0111a0001c0001t0024g0105a0001c0009t0002g0114others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3440_59-3421del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635198 | ||||||
| chr5:180635198
|
GTGGATGG others(21): Show |
G | 9 | a0001c0001t0001g0070a0001c0001t0004g0131a0002c0002t0001g0211others(6): Show | 9 | HG00642.hp2 HG02074.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3448_59-3421del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635198 | ||||||
| chr5:180635199
|
T | A | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3421A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635199 | ||||||
| chr5:180635199
|
T | C | 7 | a0001c0001t0002g0253a0001c0001t0002g0269a0001c0001t0002g0270others(4): Show | 7 | HG02129.hp1 NA18948.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3421A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635199 | ||||||
| chr5:180635201
|
G | C | 12 | a0001c0001t0001g0075a0001c0001t0001g0215a0001c0001t0002g0229others(9): Show | 12 | HG00741.hp2 HG01109.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3423C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635201
|
G | GATGC | 48 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(45): Show | 48 | HG00280.hp1 HG00423.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-3424_59-3423ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635201
|
G | GGAGGATG others(5): Show |
1 | a0024c0046t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-3424_59-3423ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635201
|
G | GGTGGATG others(173): Show |
1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3424_59-3423ins others(180): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635201
|
G | GGTGGGTG others(101): Show |
1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3424_59-3423ins others(108): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635201
|
G | T | 1 | a0002c0002t0001g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59-3423C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635201 | ||||||
| chr5:180635202
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0365a0001c0001t0002g0177others(2): Show | 5 | HG00558.hp1 HG02683.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3424T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635202 | ||||||
| chr5:180635205
|
G | C | 26 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0130others(23): Show | 26 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.59-3427C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635205 | ||||||
| chr5:180635206
|
A | G | 3 | a0001c0001t0001g0069a0002c0002t0001g0089a0002c0002t0001g0202 | 3 | HG00558.hp1 HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3428T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635206 | ||||||
| chr5:180635210
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3432T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635210 | ||||||
| chr5:180635211
|
T | C | 5 | a0001c0001t0001g0215a0001c0001t0004g0087a0002c0002t0003g0246others(2): Show | 5 | NA18954.hp1 NA18969.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3433A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635211 | ||||||
| chr5:180635211
|
T | G | 25 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0129others(22): Show | 25 | HG00423.hp1 HG00673.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.59-3433A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635211 | ||||||
| chr5:180635211
|
T | TGCATGGA others(1): Show |
3 | a0001c0001t0001g0365a0002c0002t0001g0061a0002c0002t0001g0349 | 3 | HG02683.hp1 NA18992.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.59-3434_59-3433ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635211 | ||||||
| chr5:180635213
|
G | C | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3435C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635213 | ||||||
| chr5:180635214
|
A | G | 2 | a0002c0002t0001g0089a0002c0002t0001g0202 | 2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3436T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635214 | ||||||
| chr5:180635215
|
A | T | 3 | a0001c0001t0002g0177a0002c0002t0001g0089a0002c0002t0001g0202 | 3 | HG02015.hp2 NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3437T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635215 | ||||||
| chr5:180635217
|
T | G | 3 | a0001c0001t0002g0177a0002c0002t0001g0089a0002c0002t0001g0202 | 3 | HG02015.hp2 NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3439A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635217 | ||||||
| chr5:180635218
|
A | G | 3 | a0002c0002t0001g0202a0002c0002t0001g0339a0002c0003t0003g0132 | 3 | HG02083.hp1 NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3440T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635218 | ||||||
| chr5:180635222
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0002g0177 | 2 | HG00558.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.59-3444C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635222 | ||||||
| chr5:180635223
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3445A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635223 | ||||||
| chr5:180635225
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3447C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635225 | ||||||
| chr5:180635225
|
G | GAGGGGTG others(69): Show |
1 | a0001c0001t0002g0371 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.59-3448_59-3447ins others(76): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635225 | ||||||
| chr5:180635225
|
G | T | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3447C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635225 | ||||||
| chr5:180635226
|
A | ATGGGTGG others(5): Show |
7 | a0001c0001t0001g0106a0001c0001t0002g0066a0001c0001t0002g0067others(4): Show | 7 | HG00735.hp1 NA18950.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3449_59-3448ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635226 | ||||||
| chr5:180635226
|
A | ATGGGTGG others(5): Show |
1 | a0001c0001t0001g0071 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.59-3460_59-3449dup others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635226 | ||||||
| chr5:180635226
|
A | G | 24 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0024g0105others(21): Show | 24 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.59-3448T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635226 | ||||||
| chr5:180635227
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3449A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635227 | ||||||
| chr5:180635227
|
T | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(161): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.59-3449A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635227 | ||||||
| chr5:180635230
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3452C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635230 | ||||||
| chr5:180635231
|
T | A | 1 | a0002c0002t0001g0339 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.59-3453A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635231 | ||||||
| chr5:180635234
|
G | A | 40 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.59-3456C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635234 | ||||||
| chr5:180635234
|
GTGGGTGG others(17): Show |
G | 1 | a0002c0002t0001g0331 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.59-3480_59-3457del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635234 | ||||||
| chr5:180635234
|
GTGGGTGG others(25): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-3488_59-3457del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635234 | ||||||
| chr5:180635235
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3457A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635235 | ||||||
| chr5:180635235
|
TGGGTGGA others(153): Show |
T | 8 | a0001c0001t0001g0356a0001c0001t0006g0343a0001c0001t0012g0357others(5): Show | 9 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3617_59-3458del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635235 | ||||||
| chr5:180635238
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(198): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.59-3460C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635238 | ||||||
| chr5:180635238
|
G | GTGGGTGG others(9): Show |
1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3461_59-3460ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635238 | ||||||
| chr5:180635238
|
GTGGATGG others(13): Show |
G | 1 | a0002c0002t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-3480_59-3461del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635238 | ||||||
| chr5:180635238
|
GTGGATGG others(21): Show |
G | 2 | a0002c0003t0007g0314a0002c0003t0007g0315 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.59-3488_59-3461del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635238 | ||||||
| chr5:180635238
|
GTGGATGG others(53): Show |
G | 2 | a0002c0003t0003g0108a0010c0021t0001g0326 | 2 | HG00673.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.59-3520_59-3461del others(60): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635238 | ||||||
| chr5:180635239
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3461A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635239 | ||||||
| chr5:180635239
|
T | C | 7 | a0001c0001t0002g0229a0001c0001t0002g0273a0001c0043t0002g0230others(4): Show | 7 | HG02040.hp1 HG02055.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3461A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635239 | ||||||
| chr5:180635241
|
G | C | 20 | a0001c0001t0001g0111a0001c0001t0024g0105a0001c0009t0002g0114others(17): Show | 20 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-3463C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635241 | ||||||
| chr5:180635241
|
G | GATGC | 178 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(175): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.59-3464_59-3463ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635241 | ||||||
| chr5:180635241
|
G | GGAGGATG others(5): Show |
2 | a0001c0001t0001g0365a0002c0002t0001g0349 | 2 | HG02683.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.59-3464_59-3463ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635241 | ||||||
| chr5:180635241
|
G | GGTGGGTG others(21): Show |
1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3464_59-3463ins others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635241 | ||||||
| chr5:180635241
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3463C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635241 | ||||||
| chr5:180635242
|
A | G | 38 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(35): Show | 38 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-3464T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635242 | ||||||
| chr5:180635243
|
T | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0002t0001g0341others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3465A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635243 | ||||||
| chr5:180635245
|
G | C | 8 | a0001c0001t0001g0118a0001c0001t0004g0087a0001c0032t0026g0333others(5): Show | 8 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3467C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635245 | ||||||
| chr5:180635245
|
G | GATGC | 7 | a0001c0001t0001g0106a0001c0001t0002g0066a0001c0001t0002g0067others(4): Show | 7 | HG00735.hp1 NA18950.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3468_59-3467ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635245 | ||||||
| chr5:180635246
|
A | G | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-3468T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635246 | ||||||
| chr5:180635247
|
T | A | 1 | a0002c0002t0004g0096 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-3469A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635247 | ||||||
| chr5:180635249
|
G | C | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-3471C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635249 | ||||||
| chr5:180635250
|
A | G | 26 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(23): Show | 26 | HG00423.hp2 HG01928.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.59-3472T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635250 | ||||||
| chr5:180635251
|
T | C | 14 | a0001c0001t0001g0111a0001c0001t0024g0105a0001c0009t0002g0114others(11): Show | 14 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3473A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635251 | ||||||
| chr5:180635251
|
T | G | 15 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0118others(12): Show | 15 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3473A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635251 | ||||||
| chr5:180635251
|
T | TGCATGGA others(1): Show |
5 | a0001c0001t0001g0128a0001c0001t0002g0312a0002c0002t0001g0011others(2): Show | 5 | HG01109.hp1 HG01255.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3474_59-3473ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635251 | ||||||
| chr5:180635253
|
G | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0002t0001g0341others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3475C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635253 | ||||||
| chr5:180635254
|
A | G | 4 | a0001c0001t0001g0069a0002c0002t0001g0072a0002c0003t0003g0134others(1): Show | 4 | HG00558.hp1 NA18944.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3476T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635254 | ||||||
| chr5:180635255
|
A | T | 33 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.59-3477T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635255 | ||||||
| chr5:180635257
|
T | C | 1 | a0002c0002t0004g0096 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-3479A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635257 | ||||||
| chr5:180635257
|
T | G | 32 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.59-3479A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635257 | ||||||
| chr5:180635258
|
A | G | 4 | a0001c0001t0001g0069a0002c0002t0001g0072a0002c0003t0003g0134others(1): Show | 4 | HG00558.hp1 NA18944.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3480T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635258 | ||||||
| chr5:180635261
|
G | C | 20 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(17): Show | 20 | HG00423.hp2 HG01928.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-3483C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635261 | ||||||
| chr5:180635262
|
G | A | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(31): Show | 34 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-3484C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635262 | ||||||
| chr5:180635263
|
T | C | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-3485A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635263 | ||||||
| chr5:180635265
|
G | C | 2 | a0002c0003t0003g0143a0002c0004t0033g0090 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.59-3487C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635265 | ||||||
| chr5:180635266
|
A | G | 8 | a0001c0001t0001g0069a0002c0002t0001g0084a0002c0002t0001g0205others(5): Show | 8 | HG00558.hp1 HG00609.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3488T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635266 | ||||||
| chr5:180635267
|
T | A | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0002t0001g0341others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3489A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635267 | ||||||
| chr5:180635267
|
T | G | 19 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(16): Show | 19 | HG00423.hp2 HG01928.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-3489A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635267 | ||||||
| chr5:180635269
|
G | C | 4 | a0001c0001t0002g0177a0002c0002t0001g0072a0002c0003t0003g0134others(1): Show | 4 | NA18944.hp2 NA18969.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3491C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635269 | ||||||
| chr5:180635269
|
G | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0002t0001g0341others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3491C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635269 | ||||||
| chr5:180635270
|
G | A | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(31): Show | 34 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-3492C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635270 | ||||||
| chr5:180635271
|
T | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(19): Show | 22 | HG00423.hp2 HG01928.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.59-3493A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635271 | ||||||
| chr5:180635272
|
G | A | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3494C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635272 | ||||||
| chr5:180635273
|
G | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(18): Show | 21 | HG00423.hp2 HG01928.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-3495C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635273 | ||||||
| chr5:180635273
|
GGTGGGTG others(17): Show |
G | 1 | a0002c0003t0003g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-3519_59-3496del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635273 | ||||||
| chr5:180635274
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(61): Show | 64 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-3496C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635274 | ||||||
| chr5:180635274
|
G | C | 1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.59-3496C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635274 | ||||||
| chr5:180635274
|
G | T | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3496C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635274 | ||||||
| chr5:180635275
|
T | A | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3497A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635275 | ||||||
| chr5:180635275
|
T | C | 2 | a0002c0003t0003g0143a0002c0004t0033g0090 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.59-3497A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635275 | ||||||
| chr5:180635275
|
TGGGTGGA others(113): Show |
T | 3 | a0002c0003t0003g0095a0006c0014t0009g0301a0006c0014t0009g0302 | 3 | HG02109.hp1 HG03139.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.59-3617_59-3498del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635275 | ||||||
| chr5:180635276
|
G | T | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3498C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635276 | ||||||
| chr5:180635278
|
G | A | 53 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0069others(50): Show | 53 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.59-3500C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
G | GTGGGTGG others(1): Show |
6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3501_59-3500ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
GTGGATGG others(13): Show |
G | 21 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0003g0338others(18): Show | 21 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-3520_59-3501del others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
GTGGATGG others(21): Show |
G | 5 | a0001c0001t0001g0128a0001c0001t0002g0253a0001c0001t0002g0312others(2): Show | 5 | HG00639.hp1 HG01255.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3528_59-3501del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
GTGGATGG others(29): Show |
G | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3536_59-3501del others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
GTGGATGG others(61): Show |
G | 1 | a0002c0002t0003g0076 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.59-3568_59-3501del others(68): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635278
|
GTGGATGG others(424): Show |
G | 1 | a0002c0002t0001g0354 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.59-3931_59-3501del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635278 | ||||||
| chr5:180635279
|
T | A | 2 | a0002c0003t0003g0143a0002c0004t0033g0090 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.59-3501A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635279 | ||||||
| chr5:180635279
|
T | C | 3 | a0002c0002t0001g0072a0002c0003t0003g0134a0002c0003t0003g0141 | 3 | NA18944.hp2 NA19085.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.59-3501A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635279 | ||||||
| chr5:180635281
|
G | A | 1 | a0001c0001t0012g0358 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.59-3503C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(25): Show | 28 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-3503C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | GATGC | 12 | a0001c0001t0002g0229a0001c0001t0002g0273a0001c0001t0004g0078others(9): Show | 12 | HG02027.hp1 HG02055.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3504_59-3503ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | GGAGGATG others(5): Show |
1 | a0002c0002t0001g0349 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3504_59-3503ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | GGTGGATG others(5): Show |
6 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0275others(3): Show | 6 | HG02129.hp1 NA18948.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3504_59-3503ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | GGTGGGTG others(13): Show |
1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3504_59-3503ins others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | GGTGGGTG others(13): Show |
2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3504_59-3503ins others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635281
|
G | T | 2 | a0002c0003t0003g0143a0002c0004t0033g0090 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.59-3503C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635281 | ||||||
| chr5:180635282
|
A | G | 22 | a0001c0001t0001g0070a0001c0001t0001g0106a0001c0001t0001g0129others(19): Show | 22 | HG00323.hp2 HG00733.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.59-3504T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635282 | ||||||
| chr5:180635283
|
T | A | 7 | a0001c0001t0002g0177a0001c0001t0012g0358a0002c0002t0001g0011others(4): Show | 7 | HG00323.hp2 HG01109.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3505A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635283 | ||||||
| chr5:180635285
|
G | C | 14 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0113others(11): Show | 14 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-3507C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635285 | ||||||
| chr5:180635285
|
G | T | 4 | a0001c0001t0002g0177a0002c0002t0001g0072a0002c0003t0003g0134others(1): Show | 4 | NA18944.hp2 NA18969.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3507C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635285 | ||||||
| chr5:180635286
|
A | G | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(31): Show | 34 | HG00423.hp2 HG01928.hp1 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-3508T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635286 | ||||||
| chr5:180635289
|
G | C | 8 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3511C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635289 | ||||||
| chr5:180635289
|
GATGGAAG others(25): Show |
G | 1 | a0002c0011t0014g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-3543_59-3512del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635289 | ||||||
| chr5:180635290
|
A | G | 40 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(37): Show | 40 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.59-3512T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635290 | ||||||
| chr5:180635290
|
ATGGAAGT others(5): Show |
A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.59-3524_59-3513del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635290 | ||||||
| chr5:180635291
|
T | C | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0001g0084 | 3 | NA18971.hp1 NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.59-3513A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635291 | ||||||
| chr5:180635291
|
T | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0075a0002c0002t0001g0331 | 3 | HG00558.hp1 HG00741.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.59-3513A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635291 | ||||||
| chr5:180635293
|
GAAGT | G | 23 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0070others(20): Show | 23 | HG00423.hp2 HG01928.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-3519_59-3516del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635293 | ||||||
| chr5:180635294
|
A | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0002c0002t0001g0202others(7): Show | 10 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3516T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635294 | ||||||
| chr5:180635294
|
AAGTATGG others(1): Show |
A | 4 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0005g0117others(1): Show | 4 | NA18979.hp1 NA19043.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3524_59-3517del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635294 | ||||||
| chr5:180635295
|
A | T | 15 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0001g0130others(12): Show | 15 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3517T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635295 | ||||||
| chr5:180635297
|
T | C | 2 | a0001c0001t0012g0358a0002c0002t0001g0011 | 2 | HG00323.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.59-3519A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635297 | ||||||
| chr5:180635297
|
T | G | 15 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0001g0130others(12): Show | 15 | HG00733.hp2 HG01074.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3519A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635297 | ||||||
| chr5:180635298
|
A | ATGCATGG others(29): Show |
1 | a0001c0001t0001g0106 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.59-3521_59-3520ins others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635298 | ||||||
| chr5:180635298
|
A | G | 36 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(33): Show | 36 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.59-3520T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635298 | ||||||
| chr5:180635302
|
G | A | 5 | a0001c0001t0004g0131a0001c0001t0012g0358a0002c0002t0001g0011others(2): Show | 5 | HG00323.hp2 HG01109.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3524C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635302 | ||||||
| chr5:180635304
|
G | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-3526C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635304 | ||||||
| chr5:180635305
|
G | C | 4 | a0001c0001t0004g0131a0002c0002t0001g0089a0002c0002t0001g0202others(1): Show | 4 | HG02015.hp2 HG02074.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3527C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635305 | ||||||
| chr5:180635305
|
GATGGGTG others(25): Show |
G | 1 | a0002c0002t0001g0331 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.59-3559_59-3528del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635305 | ||||||
| chr5:180635306
|
A | ATGGG | 5 | a0001c0001t0001g0069a0002c0003t0001g0243a0004c0007t0001g0015others(2): Show | 5 | HG00558.hp1 HG01496.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3532_59-3529dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | ATGGGTGG others(73): Show |
3 | a0002c0002t0001g0097a0002c0002t0004g0080a0002c0002t0004g0098 | 3 | NA18950.hp1 NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.59-3529_59-3528ins others(80): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | ATGGGTGG others(69): Show |
1 | a0001c0001t0004g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.59-3529_59-3528ins others(76): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | ATGGGTGG others(5): Show |
3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3529_59-3528ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | ATGGGTGG others(9): Show |
2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3529_59-3528ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | ATGGGTGG others(13): Show |
1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-3529_59-3528ins others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635306
|
A | G | 60 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(57): Show | 60 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-3528T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635306 | ||||||
| chr5:180635308
|
G | A | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-3530C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635308 | ||||||
| chr5:180635309
|
G | C | 5 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0005g0117others(2): Show | 5 | NA18979.hp1 NA18992.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3531C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635309 | ||||||
| chr5:180635310
|
G | A | 11 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0004g0131others(8): Show | 11 | HG00323.hp2 HG01109.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3532C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635310 | ||||||
| chr5:180635310
|
GTGGA | G | 8 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3536_59-3533del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635310 | ||||||
| chr5:180635310
|
GTGGATGG others(21): Show |
G | 1 | a0002c0002t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-3560_59-3533del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635310 | ||||||
| chr5:180635310
|
GTGGATGG others(73): Show |
G | 2 | a0002c0003t0007g0314a0002c0003t0007g0315 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.59-3612_59-3533del others(80): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635310 | ||||||
| chr5:180635311
|
T | A | 6 | a0001c0001t0001g0128a0001c0001t0002g0312a0001c0001t0003g0338others(3): Show | 6 | HG00423.hp1 HG00639.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3533A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635311 | ||||||
| chr5:180635311
|
T | C | 1 | a0001c0001t0012g0358 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.59-3533A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635311 | ||||||
| chr5:180635311
|
T | TGGGTGGG others(5): Show |
1 | a0024c0046t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-3534_59-3533ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635311 | ||||||
| chr5:180635313
|
G | T | 1 | a0002c0002t0001g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.59-3535C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635313 | ||||||
| chr5:180635314
|
A | ATGGGTGG others(9): Show |
2 | a0001c0001t0004g0078a0001c0001t0004g0087 | 2 | NA18975.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.59-3537_59-3536ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635314 | ||||||
| chr5:180635314
|
A | G | 43 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0069others(40): Show | 43 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.59-3536T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635314 | ||||||
| chr5:180635315
|
T | C | 2 | a0001c0001t0004g0131a0002c0002t0001g0089 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.59-3537A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635315 | ||||||
| chr5:180635315
|
T | G | 5 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0005g0117others(2): Show | 5 | NA18979.hp1 NA18992.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3537A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635315 | ||||||
| chr5:180635317
|
G | C | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3539C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635317 | ||||||
| chr5:180635317
|
GATGC | G | 12 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0006g0344others(9): Show | 12 | HG00609.hp2 HG00642.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3543_59-3540del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635317 | ||||||
| chr5:180635318
|
A | G | 41 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(38): Show | 41 | HG00280.hp1 HG01070.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.59-3540T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635318 | ||||||
| chr5:180635319
|
T | A | 10 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0004g0131others(7): Show | 10 | HG00323.hp2 HG02015.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3541A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635319 | ||||||
| chr5:180635319
|
T | C | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3541A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635319 | ||||||
| chr5:180635321
|
C | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3543G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | CATGGATG others(22): Show |
1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3544_59-3543ins others(29): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | CATGGATG others(33): Show |
32 | a0001c0001t0001g0062a0001c0001t0002g0372a0001c0001t0010g0368others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-3544_59-3543ins others(40): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | CATGGATG others(77): Show |
1 | a0001c0001t0001g0267 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.59-3544_59-3543ins others(84): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | CATGGATG others(77): Show |
124 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(121): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.59-3544_59-3543ins others(84): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | CATGGATG others(93): Show |
1 | a0004c0007t0001g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.59-3544_59-3543ins others(100): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(42): Show | 45 | HG00280.hp1 HG01070.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.59-3543G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0365a0001c0001t0002g0116others(8): Show | 11 | HG00323.hp2 HG02015.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3543G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635321
|
CATGG | C | 13 | a0001c0001t0001g0111a0001c0001t0002g0177a0001c0001t0020g0361others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3547_59-3544del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635321 | ||||||
| chr5:180635322
|
A | G | 8 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3544T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635322 | ||||||
| chr5:180635325
|
G | C | 8 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0004g0078others(5): Show | 8 | HG02040.hp2 HG02155.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3547C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635325 | ||||||
| chr5:180635326
|
A | G | 19 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0002g0229others(16): Show | 19 | HG00323.hp2 HG01109.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-3548T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635326 | ||||||
| chr5:180635327
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3549A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635327 | ||||||
| chr5:180635329
|
G | C | 1 | a0001c0001t0002g0253 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.59-3551C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635329 | ||||||
| chr5:180635329
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3551C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635329 | ||||||
| chr5:180635331
|
T | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(40): Show | 43 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.59-3553A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635331 | ||||||
| chr5:180635331
|
T | G | 20 | a0001c0001t0001g0075a0001c0001t0001g0111a0001c0001t0002g0066others(17): Show | 20 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-3553A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635331 | ||||||
| chr5:180635332
|
G | T | 1 | a0001c0001t0020g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-3554C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635332 | ||||||
| chr5:180635333
|
GAAGT | G | 4 | a0001c0001t0004g0131a0002c0002t0001g0089a0002c0002t0004g0093others(1): Show | 4 | HG02015.hp2 HG02074.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3559_59-3556del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635333 | ||||||
| chr5:180635334
|
A | G | 7 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0005g0117others(4): Show | 7 | HG00323.hp2 HG01109.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3556T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635334 | ||||||
| chr5:180635335
|
A | T | 8 | a0001c0001t0001g0070a0001c0001t0001g0365a0001c0001t0002g0116others(5): Show | 8 | HG00323.hp2 HG01109.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3557T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635335 | ||||||
| chr5:180635337
|
T | G | 8 | a0001c0001t0001g0070a0001c0001t0001g0365a0001c0001t0002g0116others(5): Show | 8 | HG00323.hp2 HG01109.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3559A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635337 | ||||||
| chr5:180635338
|
A | G | 9 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0004g0131others(6): Show | 9 | HG01109.hp1 HG02015.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3560T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635338 | ||||||
| chr5:180635339
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3561A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635339 | ||||||
| chr5:180635341
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3563C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635341 | ||||||
| chr5:180635342
|
G | A | 2 | a0002c0002t0004g0093a0002c0002t0013g0165 | 2 | NA18906.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3564C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635342 | ||||||
| chr5:180635346
|
A | ATGGG | 6 | a0001c0001t0001g0118a0001c0001t0001g0128a0002c0002t0001g0202others(3): Show | 6 | HG00639.hp1 HG01516.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3572_59-3569dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635346 | ||||||
| chr5:180635346
|
A | ATGGGTGG others(1): Show |
32 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(29): Show | 32 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.59-3569_59-3568ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635346 | ||||||
| chr5:180635346
|
A | ATGGGTGG others(5): Show |
7 | a0001c0001t0001g0075a0001c0001t0001g0106a0002c0002t0001g0097others(4): Show | 7 | HG00741.hp2 NA18950.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3569_59-3568ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635346 | ||||||
| chr5:180635346
|
A | G | 12 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0004g0131others(9): Show | 12 | HG00323.hp2 HG01109.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3568T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635346 | ||||||
| chr5:180635347
|
TGGGA | T | 7 | a0001c0001t0002g0273a0001c0001t0002g0297a0002c0002t0004g0033others(4): Show | 7 | HG01891.hp2 HG02129.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3573_59-3570del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635347 | ||||||
| chr5:180635348
|
G | GGGTGGGT others(4): Show |
1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3571_59-3570ins others(11): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635348 | ||||||
| chr5:180635350
|
GAGGGTGG others(25): Show |
G | 3 | a0001c0001t0001g0215a0001c0001t0002g0312a0001c0001t0020g0361 | 3 | HG02109.hp2 HG02723.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3604_59-3573del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635350 | ||||||
| chr5:180635350
|
GAGGGTGG others(69): Show |
G | 4 | a0001c0001t0002g0107a0002c0003t0003g0108a0002c0003t0003g0134others(1): Show | 4 | HG00673.hp2 NA18944.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3648_59-3573del others(76): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635350 | ||||||
| chr5:180635350
|
GAGGGTGG others(236): Show |
G | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-3815_59-3573del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635350 | ||||||
| chr5:180635351
|
A | T | 169 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(166): Show | 169 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-3573T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635351 | ||||||
| chr5:180635353
|
GGTGGGTG others(21): Show |
G | 1 | a0002c0002t0001g0337 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.59-3603_59-3576del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635353 | ||||||
| chr5:180635354
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3576C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635354 | ||||||
| chr5:180635354
|
G | GTGGA | 8 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3577_59-3576ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635354 | ||||||
| chr5:180635355
|
T | G | 2 | a0001c0001t0012g0358a0002c0002t0004g0093 | 2 | HG00323.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3577A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635355 | ||||||
| chr5:180635357
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.59-3579C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635357 | ||||||
| chr5:180635358
|
G | A | 7 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0005g0117others(4): Show | 7 | HG00323.hp2 HG01109.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3580C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635358 | ||||||
| chr5:180635358
|
G | GTGGGTGG others(9): Show |
1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3581_59-3580ins others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635358 | ||||||
| chr5:180635360
|
G | GA | 3 | a0002c0002t0001g0205a0002c0002t0004g0203a0002c0002t0004g0204 | 3 | HG00609.hp2 NA18993.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.59-3583_59-3582ins others(1): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635360 | ||||||
| chr5:180635360
|
GGATGGAT others(68): Show |
G | 1 | a0002c0003t0005g0103 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.59-3657_59-3583del others(75): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635360 | ||||||
| chr5:180635361
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3583C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635361 | ||||||
| chr5:180635362
|
A | G | 48 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.59-3584T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635362 | ||||||
| chr5:180635362
|
ATGGATGG others(285): Show |
A | 3 | a0002c0002t0001g0205a0002c0002t0004g0203a0002c0002t0004g0204 | 3 | HG00609.hp2 NA18993.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.59-3876_59-3585del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635362 | ||||||
| chr5:180635363
|
T | A | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3585A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635363 | ||||||
| chr5:180635363
|
T | C | 3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3585A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635363 | ||||||
| chr5:180635365
|
G | C | 27 | a0001c0001t0001g0070a0001c0001t0001g0111a0001c0001t0001g0113others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-3587C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635365 | ||||||
| chr5:180635366
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0118a0001c0001t0003g0338others(1): Show | 4 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3588T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635366 | ||||||
| chr5:180635368
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3590C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635368 | ||||||
| chr5:180635368
|
G | GGATGGAA others(76): Show |
1 | a0007c0010t0015g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.59-3591_59-3590ins others(83): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635368 | ||||||
| chr5:180635369
|
G | C | 29 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0128others(26): Show | 29 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3591C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635369 | ||||||
| chr5:180635370
|
A | ATGGAAGT others(197): Show |
1 | a0001c0001t0001g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.59-3593_59-3592ins others(204): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635370 | ||||||
| chr5:180635370
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0002g0253a0001c0001t0003g0338others(1): Show | 4 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3592T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635370 | ||||||
| chr5:180635373
|
G | C | 7 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(4): Show | 7 | HG00642.hp2 HG02040.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3595C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635373 | ||||||
| chr5:180635373
|
G | T | 10 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3595C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635373 | ||||||
| chr5:180635375
|
T | C | 6 | a0001c0001t0001g0365a0001c0001t0002g0116a0001c0001t0004g0087others(3): Show | 6 | HG01109.hp1 NA18975.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3597A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635375 | ||||||
| chr5:180635375
|
T | G | 17 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0128others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-3597A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635375 | ||||||
| chr5:180635379
|
A | T | 9 | a0001c0001t0001g0071a0001c0001t0003g0338a0001c0001t0006g0344others(6): Show | 9 | HG00423.hp1 HG00642.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3601T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635379 | ||||||
| chr5:180635381
|
T | C | 3 | a0001c0001t0003g0338a0002c0003t0003g0088a0002c0003t0003g0190 | 3 | HG00423.hp1 HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.59-3603A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635381 | ||||||
| chr5:180635381
|
T | G | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3603A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635381 | ||||||
| chr5:180635385
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3607C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635385 | ||||||
| chr5:180635385
|
G | GATGGATG others(1): Show |
11 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3608_59-3607ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635385 | ||||||
| chr5:180635386
|
G | A | 11 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0002g0312others(8): Show | 11 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3608C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635386 | ||||||
| chr5:180635387
|
T | A | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3609A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635387 | ||||||
| chr5:180635387
|
T | C | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3609A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635387 | ||||||
| chr5:180635389
|
G | T | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3611C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635389 | ||||||
| chr5:180635390
|
A | ATGGG | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(31): Show | 34 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-3616_59-3613dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635390 | ||||||
| chr5:180635390
|
A | ATGGGTGG others(5): Show |
12 | a0001c0001t0001g0111a0001c0001t0002g0066a0001c0001t0004g0078others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3613_59-3612ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635390 | ||||||
| chr5:180635390
|
A | ATGGGTGG others(5): Show |
1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-3613_59-3612ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635390 | ||||||
| chr5:180635390
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0002g0312a0001c0001t0020g0361others(1): Show | 4 | HG01255.hp1 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3612T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635390 | ||||||
| chr5:180635391
|
T | C | 2 | a0001c0001t0003g0338a0002c0003t0003g0088 | 2 | HG00423.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.59-3613A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635391 | ||||||
| chr5:180635391
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3613A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635391 | ||||||
| chr5:180635394
|
G | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0003g0338others(6): Show | 9 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3616C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635394 | ||||||
| chr5:180635394
|
G | GTGGATGG others(6): Show |
1 | a0001c0001t0002g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.59-3617_59-3616ins others(13): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635394 | ||||||
| chr5:180635394
|
GAGGGTGG others(25): Show |
G | 5 | a0001c0001t0001g0070a0001c0001t0001g0113a0001c0001t0001g0365others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3648_59-3617del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635394 | ||||||
| chr5:180635395
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.59-3617T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635395 | ||||||
| chr5:180635395
|
A | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(226): Show | 236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.59-3617T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635395 | ||||||
| chr5:180635397
|
G | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0003g0338others(6): Show | 9 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3619C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635397 | ||||||
| chr5:180635397
|
GGTGGGTG others(21): Show |
G | 3 | a0001c0001t0024g0105a0002c0002t0003g0076a0002c0003t0003g0104 | 3 | NA18747.hp1 NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.59-3647_59-3620del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635397 | ||||||
| chr5:180635398
|
G | A | 12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0003g0338others(9): Show | 12 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3620C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635398 | ||||||
| chr5:180635402
|
GTGGATGG others(300): Show |
G | 1 | a0010c0021t0001g0326 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.59-3931_59-3625del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635402 | ||||||
| chr5:180635403
|
TGGATGGA others(29): Show |
T | 1 | a0001c0001t0002g0253 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.59-3661_59-3626del others(36): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635403 | ||||||
| chr5:180635406
|
A | G | 10 | a0001c0001t0001g0092a0001c0001t0004g0087a0001c0001t0004g0142others(7): Show | 10 | HG01255.hp1 HG02027.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-3628T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635406 | ||||||
| chr5:180635409
|
G | A | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3631C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635409 | ||||||
| chr5:180635409
|
G | C | 31 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0118others(28): Show | 31 | HG00323.hp2 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-3631C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635409 | ||||||
| chr5:180635409
|
GATGGATG others(9): Show |
G | 2 | a0001c0001t0003g0338a0002c0003t0003g0088 | 2 | HG00423.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.59-3647_59-3632del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635409 | ||||||
| chr5:180635410
|
A | G | 12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0005g0117others(9): Show | 12 | HG00558.hp1 HG00642.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3632T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635410 | ||||||
| chr5:180635412
|
G | A | 11 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3634C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635412 | ||||||
| chr5:180635413
|
G | C | 64 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(61): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.59-3635C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635413 | ||||||
| chr5:180635413
|
GATGGATG others(5): Show |
G | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.59-3647_59-3636del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635413 | ||||||
| chr5:180635414
|
A | ATGGAAGT others(25): Show |
1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3637_59-3636ins others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635414 | ||||||
| chr5:180635414
|
A | G | 5 | a0001c0001t0005g0117a0002c0002t0004g0093a0002c0002t0013g0165others(2): Show | 5 | HG02040.hp1 HG02155.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3636T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635414 | ||||||
| chr5:180635415
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3637A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635415 | ||||||
| chr5:180635417
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3639C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635417 | ||||||
| chr5:180635417
|
GATGGAAG others(1): Show |
G | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3647_59-3640del others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635417 | ||||||
| chr5:180635419
|
T | C | 1 | a0002c0004t0031g0279 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.59-3641A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635419 | ||||||
| chr5:180635419
|
T | G | 18 | a0001c0001t0001g0111a0001c0001t0001g0215a0001c0001t0002g0066others(15): Show | 18 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3641A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635419 | ||||||
| chr5:180635422
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3644T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635422 | ||||||
| chr5:180635422
|
AAGTATGG others(17): Show |
A | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.59-3668_59-3645del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635422 | ||||||
| chr5:180635423
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3645T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635423 | ||||||
| chr5:180635425
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3647A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635425 | ||||||
| chr5:180635426
|
A | G | 8 | a0001c0001t0001g0071a0001c0001t0003g0338a0001c0001t0006g0344others(5): Show | 8 | HG00423.hp1 HG00642.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3648T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635426 | ||||||
| chr5:180635429
|
G | C | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3651C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635429 | ||||||
| chr5:180635430
|
G | A | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3652C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635430 | ||||||
| chr5:180635433
|
GATGGGAG others(25): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-3687_59-3656del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635433 | ||||||
| chr5:180635434
|
A | ATGGGTGG others(5): Show |
5 | a0001c0001t0001g0075a0002c0002t0001g0097a0002c0002t0004g0096others(2): Show | 5 | HG00741.hp2 NA18950.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3657_59-3656ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635434 | ||||||
| chr5:180635434
|
A | G | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-3656T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635434 | ||||||
| chr5:180635435
|
T | G | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3657A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635435 | ||||||
| chr5:180635435
|
TGGGA | T | 49 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(46): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.59-3661_59-3658del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635435 | ||||||
| chr5:180635438
|
G | A | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3660C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635438 | ||||||
| chr5:180635439
|
A | G | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3661T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635439 | ||||||
| chr5:180635439
|
A | T | 66 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(63): Show | 66 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.59-3661T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635439 | ||||||
| chr5:180635441
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3663C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635441 | ||||||
| chr5:180635441
|
G | T | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3663C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635441 | ||||||
| chr5:180635442
|
G | A | 18 | a0001c0001t0001g0071a0001c0001t0001g0106a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG00642.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-3664C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635442 | ||||||
| chr5:180635442
|
G | GAGGATGG others(5): Show |
1 | a0001c0001t0001g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-3665_59-3664ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635442 | ||||||
| chr5:180635446
|
G | A | 63 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(60): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.59-3668C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635446 | ||||||
| chr5:180635446
|
G | GTGAGAGG others(13): Show |
1 | a0002c0003t0003g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.59-3669_59-3668ins others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635446 | ||||||
| chr5:180635446
|
G | GTGGA | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3672_59-3669dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635446 | ||||||
| chr5:180635447
|
T | C | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3669A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635447 | ||||||
| chr5:180635449
|
G | C | 2 | a0002c0002t0001g0345a0002c0002t0013g0165 | 2 | HG00639.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.59-3671C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635449 | ||||||
| chr5:180635449
|
G | GGTGGATG others(5): Show |
3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3672_59-3671ins others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635449 | ||||||
| chr5:180635449
|
G | GGTGGGTG others(13): Show |
2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-3672_59-3671ins others(20): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635449 | ||||||
| chr5:180635449
|
G | GGTGGGTG others(69): Show |
1 | a0002c0002t0004g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.59-3672_59-3671ins others(76): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635449 | ||||||
| chr5:180635450
|
A | G | 34 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0128others(31): Show | 34 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-3672T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635450 | ||||||
| chr5:180635450
|
ATGGATGG others(197): Show |
A | 1 | a0001c0001t0005g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.59-3876_59-3673del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635450 | ||||||
| chr5:180635453
|
G | C | 12 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0002g0253others(9): Show | 12 | HG00558.hp1 HG00642.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3675C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635453 | ||||||
| chr5:180635453
|
G | GATGC | 5 | a0001c0001t0001g0075a0002c0002t0001g0097a0002c0002t0004g0096others(2): Show | 5 | HG00741.hp2 NA18950.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3676_59-3675ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635453 | ||||||
| chr5:180635454
|
A | G | 24 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0128others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-3676T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635454 | ||||||
| chr5:180635455
|
T | C | 2 | a0001c0001t0001g0092a0002c0003t0003g0074 | 2 | HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.59-3677A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635455 | ||||||
| chr5:180635457
|
G | C | 3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3679C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635457 | ||||||
| chr5:180635458
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0128others(18): Show | 21 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-3680T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635458 | ||||||
| chr5:180635459
|
T | C | 4 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0004g0080others(1): Show | 4 | NA18906.hp1 NA18971.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3681A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635459 | ||||||
| chr5:180635459
|
T | G | 9 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0024g0105others(6): Show | 9 | HG00558.hp1 HG00741.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3681A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635459 | ||||||
| chr5:180635461
|
G | C | 12 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(9): Show | 12 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3683C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635461 | ||||||
| chr5:180635461
|
GAAGT | G | 3 | a0001c0001t0001g0128a0002c0002t0001g0202a0002c0002t0001g0349 | 3 | HG02683.hp1 HG03654.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3687_59-3684del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635461 | ||||||
| chr5:180635462
|
A | G | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-3684T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635462 | ||||||
| chr5:180635463
|
A | T | 31 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0002g0229others(28): Show | 31 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-3685T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635463 | ||||||
| chr5:180635465
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-3687A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635465 | ||||||
| chr5:180635465
|
T | G | 29 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0002g0229others(26): Show | 29 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3687A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635465 | ||||||
| chr5:180635466
|
A | G | 5 | a0001c0001t0001g0128a0002c0002t0001g0202a0002c0002t0001g0349others(2): Show | 5 | HG02155.hp1 HG02683.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3688T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635466 | ||||||
| chr5:180635467
|
T | A | 1 | a0001c0001t0002g0253 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.59-3689A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635467 | ||||||
| chr5:180635469
|
G | C | 17 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0004g0078others(14): Show | 17 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-3691C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635469 | ||||||
| chr5:180635470
|
G | A | 30 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0002g0229others(27): Show | 30 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.59-3692C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635470 | ||||||
| chr5:180635471
|
T | A | 12 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(9): Show | 12 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3693A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635471 | ||||||
| chr5:180635473
|
G | T | 12 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(9): Show | 12 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3695C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635473 | ||||||
| chr5:180635474
|
A | G | 2 | a0002c0002t0004g0093a0002c0003t0003g0143 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3696T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635474 | ||||||
| chr5:180635475
|
T | A | 11 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3697A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635475 | ||||||
| chr5:180635475
|
T | C | 1 | a0001c0001t0002g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.59-3697A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635475 | ||||||
| chr5:180635475
|
T | G | 5 | a0001c0001t0001g0106a0001c0001t0004g0131a0002c0002t0001g0084others(2): Show | 5 | HG02015.hp2 HG02074.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3697A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635475 | ||||||
| chr5:180635478
|
G | A | 23 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0128others(20): Show | 23 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-3700C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635478 | ||||||
| chr5:180635478
|
GTGGGTGG others(216): Show |
G | 2 | a0001c0001t0001g0092a0002c0003t0003g0074 | 2 | HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.59-3923_59-3701del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635478 | ||||||
| chr5:180635478
|
GTGGGTGG others(276): Show |
G | 6 | a0001c0001t0001g0071a0001c0001t0006g0344a0002c0002t0001g0211others(3): Show | 6 | HG00642.hp2 HG03491.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3983_59-3701del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635478 | ||||||
| chr5:180635479
|
T | A | 6 | a0001c0001t0001g0106a0001c0001t0002g0312a0001c0001t0004g0131others(3): Show | 6 | HG02015.hp2 HG02074.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3701A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635479 | ||||||
| chr5:180635479
|
T | C | 12 | a0001c0001t0001g0111a0001c0001t0004g0078a0001c0009t0002g0114others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3701A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635479 | ||||||
| chr5:180635481
|
G | C | 3 | a0001c0001t0001g0128a0002c0002t0001g0202a0002c0002t0001g0349 | 3 | HG02683.hp1 HG03654.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.59-3703C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635481 | ||||||
| chr5:180635481
|
G | T | 6 | a0001c0001t0001g0106a0001c0001t0002g0312a0001c0001t0004g0131others(3): Show | 6 | HG02015.hp2 HG02074.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3703C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635481 | ||||||
| chr5:180635482
|
G | A | 39 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0128others(36): Show | 39 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-3704C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635482 | ||||||
| chr5:180635482
|
GTGGGTGG others(488): Show |
G | 1 | a0002c0004t0031g0279 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.59-4199_59-3705del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635482 | ||||||
| chr5:180635483
|
T | A | 12 | a0001c0001t0001g0111a0001c0001t0004g0078a0001c0009t0002g0114others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3705A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635483 | ||||||
| chr5:180635485
|
G | A | 4 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0190others(1): Show | 4 | HG02040.hp1 HG02129.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3707C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635485 | ||||||
| chr5:180635485
|
G | C | 1 | a0002c0003t0003g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.59-3707C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635485 | ||||||
| chr5:180635485
|
G | T | 12 | a0001c0001t0001g0111a0001c0001t0004g0078a0001c0009t0002g0114others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3707C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635485 | ||||||
| chr5:180635486
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0128a0001c0001t0001g0360others(16): Show | 19 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.59-3708C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635486 | ||||||
| chr5:180635486
|
GTGGTGGG others(72): Show |
G | 3 | a0001c0001t0003g0338a0002c0002t0001g0011a0002c0003t0005g0103 | 3 | HG00423.hp1 HG01109.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.59-3787_59-3709del others(79): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635486 | ||||||
| chr5:180635486
|
GTGGTGGG others(132): Show |
G | 5 | a0001c0001t0001g0365a0001c0001t0002g0107a0002c0003t0003g0108others(2): Show | 5 | HG00673.hp2 NA18944.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3847_59-3709del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635486 | ||||||
| chr5:180635486
|
GTGGTGGG others(216): Show |
G | 9 | a0001c0001t0001g0356a0001c0001t0012g0357a0002c0002t0001g0002others(6): Show | 10 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-3931_59-3709del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635486 | ||||||
| chr5:180635487
|
T | TG | 9 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0004g0142others(6): Show | 9 | HG00741.hp2 HG02027.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-3710dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635487 | ||||||
| chr5:180635487
|
TGGTG | T | 10 | a0001c0001t0001g0106a0001c0001t0001g0128a0001c0001t0002g0312others(7): Show | 10 | HG02015.hp2 HG02040.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3713_59-3710del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635487 | ||||||
| chr5:180635488
|
GGTGGGAT others(24): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-3741_59-3711del others(31): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635488 | ||||||
| chr5:180635488
|
GGTGGGAT others(35): Show |
G | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-3752_59-3711del others(42): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635488 | ||||||
| chr5:180635488
|
GGTGGGAT others(43): Show |
G | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3760_59-3711del others(50): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635488 | ||||||
| chr5:180635488
|
GGTGGGAT others(95): Show |
G | 1 | a0002c0003t0006g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59-3812_59-3711del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635488 | ||||||
| chr5:180635488
|
GGTGGGAT others(155): Show |
G | 33 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(30): Show | 33 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.59-3872_59-3711del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635488 | ||||||
| chr5:180635489
|
G | A | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3711C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
G | GAAGTATG others(178): Show |
1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3712_59-3711ins others(185): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
G | GATGCA | 24 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(21): Show | 24 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-3712_59-3711ins others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
G | GATGGA | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3712_59-3711ins others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
G | GGTGGATG others(6): Show |
1 | a0004c0007t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-3712_59-3711ins others(13): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
G | GGTGGGTG others(6): Show |
4 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0004g0080others(1): Show | 4 | NA18971.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3712_59-3711ins others(13): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635489
|
GTGGGATG others(5): Show |
G | 2 | a0001c0001t0002g0116a0002c0002t0001g0345 | 2 | HG00639.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.59-3723_59-3712del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635489 | ||||||
| chr5:180635490
|
T | A | 15 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(12): Show | 15 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3712A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635490 | ||||||
| chr5:180635490
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(232): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.59-3712A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635490 | ||||||
| chr5:180635491
|
G | A | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3713C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635491 | ||||||
| chr5:180635491
|
G | GGAT | 32 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0066others(29): Show | 32 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-3714_59-3713ins others(3): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635491 | ||||||
| chr5:180635491
|
G | GGGTGGGT others(16): Show |
5 | a0001c0001t0001g0075a0001c0001t0004g0142a0002c0002t0001g0097others(2): Show | 5 | HG00741.hp2 HG02027.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3714_59-3713ins others(23): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635491 | ||||||
| chr5:180635491
|
G | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(246): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.59-3713C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635491 | ||||||
| chr5:180635492
|
G | T | 1 | a0001c0001t0002g0253 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.59-3714C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635492 | ||||||
| chr5:180635493
|
G | C | 1 | a0002c0002t0004g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.59-3715C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635493 | ||||||
| chr5:180635493
|
GATGGAAG others(21): Show |
G | 4 | a0001c0001t0001g0070a0001c0001t0024g0105a0002c0002t0013g0165others(1): Show | 4 | NA18612.hp2 NA18906.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3743_59-3716del others(28): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635493 | ||||||
| chr5:180635494
|
A | G | 12 | a0001c0001t0001g0215a0001c0001t0002g0229a0001c0001t0002g0269others(9): Show | 12 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3716T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635494 | ||||||
| chr5:180635495
|
T | C | 9 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0004g0142others(6): Show | 9 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3717A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635495 | ||||||
| chr5:180635497
|
GAAGT | G | 18 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0215others(15): Show | 18 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3723_59-3720del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635497 | ||||||
| chr5:180635498
|
A | G | 13 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(10): Show | 13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3720T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635498 | ||||||
| chr5:180635499
|
A | T | 14 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(11): Show | 14 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-3721T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635499 | ||||||
| chr5:180635501
|
T | A | 11 | a0001c0001t0002g0229a0001c0001t0002g0269a0001c0001t0002g0270others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3723A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635501 | ||||||
| chr5:180635501
|
T | C | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3723A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635501 | ||||||
| chr5:180635501
|
T | G | 2 | a0002c0002t0001g0089a0002c0003t0003g0190 | 2 | HG02015.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.59-3723A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635501 | ||||||
| chr5:180635502
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(214): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.59-3724C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635502 | ||||||
| chr5:180635505
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-3727C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635505 | ||||||
| chr5:180635506
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0215a0001c0001t0004g0087 | 3 | NA18975.hp2 NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3728C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635506 | ||||||
| chr5:180635510
|
A | G | 22 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0360others(19): Show | 22 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-3732T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635510 | ||||||
| chr5:180635511
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-3733A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635511 | ||||||
| chr5:180635512
|
GGGAGGGT | G | 3 | a0001c0001t0001g0069a0001c0001t0002g0116a0002c0002t0003g0076 | 3 | HG00558.hp1 NA18747.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.59-3741_59-3735del others(7): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635512 | ||||||
| chr5:180635513
|
G | C | 12 | a0001c0001t0002g0229a0001c0001t0002g0253a0001c0001t0002g0269others(9): Show | 12 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-3735C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635513 | ||||||
| chr5:180635513
|
G | T | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3735C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635513 | ||||||
| chr5:180635514
|
G | A | 15 | a0001c0001t0001g0118a0001c0001t0002g0229a0001c0001t0002g0253others(12): Show | 15 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3736C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635514 | ||||||
| chr5:180635514
|
GAGGGTGA others(120): Show |
G | 1 | a0002c0003t0003g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-3863_59-3737del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635514 | ||||||
| chr5:180635515
|
A | C | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3737T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635515 | ||||||
| chr5:180635515
|
A | T | 72 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0075others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.59-3737T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635515 | ||||||
| chr5:180635516
|
G | C | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3738C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635516 | ||||||
| chr5:180635516
|
GGGT | G | 13 | a0001c0001t0001g0118a0001c0001t0002g0229a0001c0001t0002g0253others(10): Show | 13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3741_59-3739del others(3): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635516 | ||||||
| chr5:180635517
|
G | A | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3739C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635517 | ||||||
| chr5:180635518
|
G | A | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3740C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635518 | ||||||
| chr5:180635518
|
G | T | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3740C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635518 | ||||||
| chr5:180635518
|
GTGA | G | 17 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0002g0312others(14): Show | 17 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-3743_59-3741del others(3): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635518 | ||||||
| chr5:180635519
|
T | A | 1 | a0002c0003t0003g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.59-3741A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635519 | ||||||
| chr5:180635519
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.59-3741A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635519 | ||||||
| chr5:180635519
|
T | TG | 219 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(216): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.59-3742dupC | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635519 | ||||||
| chr5:180635519
|
T | TGGGTG | 16 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0001g0268others(13): Show | 16 | HG00741.hp2 HG02257.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3742_59-3741ins others(5): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635519 | ||||||
| chr5:180635519
|
T | TGGGTGGG others(2): Show |
4 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0004g0080others(1): Show | 4 | NA18971.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3742_59-3741ins others(9): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635519 | ||||||
| chr5:180635520
|
G | GGATGGAA others(2): Show |
21 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-3743_59-3742ins others(9): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635520 | ||||||
| chr5:180635520
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0215 | 2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3742C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635520 | ||||||
| chr5:180635521
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(218): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.59-3743T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635521 | ||||||
| chr5:180635524
|
G | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0268a0001c0047t0001g0173others(6): Show | 9 | HG00558.hp1 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-3746C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635524 | ||||||
| chr5:180635525
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0070others(59): Show | 62 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.59-3747T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635525 | ||||||
| chr5:180635526
|
T | A | 2 | a0001c0001t0002g0306a0004c0007t0001g0015 | 2 | HG01496.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3748A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635526 | ||||||
| chr5:180635528
|
G | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.59-3750C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635528 | ||||||
| chr5:180635528
|
G | T | 2 | a0001c0001t0002g0306a0004c0007t0001g0015 | 2 | HG01496.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3750C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635528 | ||||||
| chr5:180635529
|
A | G | 10 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0004g0142others(7): Show | 10 | HG00741.hp2 HG02027.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-3751T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635529 | ||||||
| chr5:180635530
|
T | A | 13 | a0001c0001t0002g0229a0001c0001t0002g0253a0001c0001t0002g0269others(10): Show | 13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3752A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635530 | ||||||
| chr5:180635531
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-3753C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635531 | ||||||
| chr5:180635532
|
G | A | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-3754C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635532 | ||||||
| chr5:180635532
|
G | C | 3 | a0001c0001t0001g0113a0001c0001t0006g0209a0002c0002t0004g0093 | 3 | HG01981.hp2 NA19091.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.59-3754C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635532 | ||||||
| chr5:180635532
|
G | T | 13 | a0001c0001t0002g0229a0001c0001t0002g0253a0001c0001t0002g0269others(10): Show | 13 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.59-3754C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635532 | ||||||
| chr5:180635533
|
A | G | 29 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0118others(26): Show | 29 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.59-3755T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635533 | ||||||
| chr5:180635534
|
T | A | 3 | a0001c0001t0001g0360a0002c0002t0001g0061a0005c0018t0013g0167 | 3 | HG02257.hp2 HG02976.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.59-3756A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635534 | ||||||
| chr5:180635534
|
T | C | 2 | a0001c0001t0001g0069a0002c0002t0003g0076 | 2 | HG00558.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.59-3756A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635534 | ||||||
| chr5:180635534
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-3756A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635534 | ||||||
| chr5:180635536
|
G | C | 12 | a0001c0001t0001g0106a0001c0001t0002g0273a0001c0001t0004g0131others(9): Show | 12 | HG00639.hp1 HG02074.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3758C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635536 | ||||||
| chr5:180635536
|
G | T | 2 | a0001c0001t0001g0360a0005c0018t0013g0167 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.59-3758C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635536 | ||||||
| chr5:180635537
|
A | G | 16 | a0001c0001t0001g0118a0001c0001t0001g0215a0001c0001t0002g0229others(13): Show | 16 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3759T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635537 | ||||||
| chr5:180635538
|
T | A | 67 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0069others(64): Show | 67 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.59-3760A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635538 | ||||||
| chr5:180635538
|
T | C | 2 | a0002c0002t0001g0089a0002c0002t0004g0093 | 2 | HG02015.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.59-3760A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635538 | ||||||
| chr5:180635539
|
G | A | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3761C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635539 | ||||||
| chr5:180635540
|
G | T | 70 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0069others(67): Show | 70 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.59-3762C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635540 | ||||||
| chr5:180635541
|
A | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0118others(27): Show | 30 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.59-3763T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635541 | ||||||
| chr5:180635541
|
AT | A | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3764delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635541 | ||||||
| chr5:180635542
|
T | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(168): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.59-3764A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635542 | ||||||
| chr5:180635544
|
G | C | 3 | a0002c0002t0001g0061a0002c0002t0001g0115a0002c0002t0001g0254 | 3 | NA18612.hp1 NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3766C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635544 | ||||||
| chr5:180635544
|
G | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(168): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.59-3766C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635544 | ||||||
| chr5:180635545
|
A | G | 105 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.59-3767T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635545 | ||||||
| chr5:180635546
|
T | A | 11 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0002g0273others(8): Show | 11 | HG00741.hp2 HG02129.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3768A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635546 | ||||||
| chr5:180635546
|
T | C | 7 | a0001c0001t0001g0106a0001c0001t0004g0131a0001c0001t0024g0105others(4): Show | 7 | HG00639.hp1 HG02074.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3768A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635546 | ||||||
| chr5:180635548
|
G | T | 11 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0002g0273others(8): Show | 11 | HG00741.hp2 HG02129.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3770C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635548 | ||||||
| chr5:180635549
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(211): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.59-3771T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635549 | ||||||
| chr5:180635550
|
T | A | 11 | a0001c0001t0001g0106a0001c0001t0004g0131a0001c0001t0004g0142others(8): Show | 11 | HG00639.hp1 HG02027.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3772A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635550 | ||||||
| chr5:180635552
|
G | C | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3774C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635552 | ||||||
| chr5:180635552
|
G | T | 11 | a0001c0001t0001g0106a0001c0001t0004g0131a0001c0001t0004g0142others(8): Show | 11 | HG00639.hp1 HG02027.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-3774C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635552 | ||||||
| chr5:180635553
|
A | G | 112 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(109): Show | 112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.59-3775T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635553 | ||||||
| chr5:180635554
|
T | G | 1 | a0001c0001t0004g0087 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.59-3776A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635554 | ||||||
| chr5:180635556
|
G | C | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3778C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635556 | ||||||
| chr5:180635557
|
A | G | 110 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0069others(107): Show | 110 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.59-3779T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635557 | ||||||
| chr5:180635558
|
T | C | 2 | a0002c0002t0001g0061a0002c0002t0001g0115 | 2 | NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3780A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635558 | ||||||
| chr5:180635560
|
G | A | 3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3782C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635560 | ||||||
| chr5:180635561
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(243): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.59-3783T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635561 | ||||||
| chr5:180635564
|
G | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0118others(21): Show | 24 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-3786C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635564 | ||||||
| chr5:180635565
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(195): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.59-3787T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635565 | ||||||
| chr5:180635566
|
T | A | 2 | a0002c0002t0001g0061a0002c0002t0001g0115 | 2 | NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3788A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635566 | ||||||
| chr5:180635566
|
T | C | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3788A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635566 | ||||||
| chr5:180635568
|
G | C | 69 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(66): Show | 69 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.59-3790C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635568 | ||||||
| chr5:180635568
|
G | T | 2 | a0002c0002t0001g0061a0002c0002t0001g0115 | 2 | NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3790C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635568 | ||||||
| chr5:180635569
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(195): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.59-3791T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635569 | ||||||
| chr5:180635570
|
T | A | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3792A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635570 | ||||||
| chr5:180635572
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3794C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635572 | ||||||
| chr5:180635572
|
G | C | 3 | a0001c0001t0001g0268a0001c0001t0002g0306a0004c0007t0001g0015 | 3 | HG01496.hp2 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.59-3794C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635572 | ||||||
| chr5:180635572
|
G | T | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3794C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635572 | ||||||
| chr5:180635573
|
A | G | 29 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0106others(26): Show | 29 | HG00558.hp1 HG00639.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-3795T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635573 | ||||||
| chr5:180635574
|
T | A | 8 | a0001c0001t0001g0360a0001c0001t0002g0066a0001c0001t0002g0067others(5): Show | 8 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3796A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635574 | ||||||
| chr5:180635574
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0215 | 2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.59-3796A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635574 | ||||||
| chr5:180635576
|
G | C | 6 | a0001c0047t0001g0173a0002c0003t0001g0375a0002c0022t0003g0147others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3798C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635576 | ||||||
| chr5:180635576
|
G | T | 8 | a0001c0001t0001g0360a0001c0001t0002g0066a0001c0001t0002g0067others(5): Show | 8 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3798C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635576 | ||||||
| chr5:180635577
|
A | AAGTATGG others(329): Show |
1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3800_59-3799ins others(336): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635577 | ||||||
| chr5:180635577
|
A | G | 15 | a0001c0001t0001g0106a0001c0001t0002g0273a0001c0001t0004g0131others(12): Show | 15 | HG00639.hp1 HG02015.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3799T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635577 | ||||||
| chr5:180635578
|
T | A | 39 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0113others(36): Show | 39 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-3800A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635578 | ||||||
| chr5:180635580
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(168): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.59-3802C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635580 | ||||||
| chr5:180635580
|
G | T | 39 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0113others(36): Show | 39 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-3802C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635580 | ||||||
| chr5:180635581
|
A | G | 17 | a0001c0001t0001g0106a0001c0001t0001g0360a0001c0001t0002g0066others(14): Show | 17 | HG00639.hp1 HG02074.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-3803T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635581 | ||||||
| chr5:180635582
|
T | A | 69 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(66): Show | 69 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.59-3804A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635582 | ||||||
| chr5:180635584
|
G | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0002g0116others(10): Show | 13 | HG00741.hp2 HG02027.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3806C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635584 | ||||||
| chr5:180635584
|
G | T | 55 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(52): Show | 55 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.59-3806C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635584 | ||||||
| chr5:180635585
|
A | G | 46 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0106others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.59-3807T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635585 | ||||||
| chr5:180635586
|
T | A | 4 | a0001c0001t0001g0268a0001c0001t0002g0306a0002c0002t0001g0254others(1): Show | 4 | HG01496.hp2 NA18612.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3808A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635586 | ||||||
| chr5:180635586
|
T | G | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3808A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635586 | ||||||
| chr5:180635587
|
G | A | 3 | a0001c0001t0002g0273a0002c0002t0004g0033a0002c0003t0003g0274 | 3 | HG02129.hp2 NA18970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3809C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635587 | ||||||
| chr5:180635588
|
G | C | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3810C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635588 | ||||||
| chr5:180635588
|
G | T | 4 | a0001c0001t0001g0268a0001c0001t0002g0306a0002c0002t0001g0254others(1): Show | 4 | HG01496.hp2 NA18612.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3810C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635588 | ||||||
| chr5:180635589
|
A | G | 66 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(63): Show | 66 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.59-3811T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635589 | ||||||
| chr5:180635590
|
T | A | 26 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3812A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635590 | ||||||
| chr5:180635591
|
G | A | 1 | a0002c0003t0006g0334 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59-3813C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635591 | ||||||
| chr5:180635592
|
G | GAAGTATG others(89): Show |
3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3815_59-3814ins others(96): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635592 | ||||||
| chr5:180635592
|
G | T | 26 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(23): Show | 26 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3814C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635592 | ||||||
| chr5:180635593
|
A | G | 51 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0113others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.59-3815T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635593 | ||||||
| chr5:180635594
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(158): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.59-3816A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635594 | ||||||
| chr5:180635594
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-3816A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635594 | ||||||
| chr5:180635594
|
T | TGGGTGAG others(1): Show |
4 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0004g0080others(1): Show | 4 | NA18971.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3817_59-3816ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635594 | ||||||
| chr5:180635596
|
G | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(158): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.59-3818C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635596 | ||||||
| chr5:180635597
|
A | G | 57 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0069others(54): Show | 57 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.59-3819T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635597 | ||||||
| chr5:180635598
|
T | A | 4 | a0001c0001t0002g0116a0001c0001t0006g0209a0002c0002t0004g0033others(1): Show | 4 | HG02129.hp2 NA19066.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3820A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635598 | ||||||
| chr5:180635600
|
G | T | 4 | a0001c0001t0002g0116a0001c0001t0006g0209a0002c0002t0004g0033others(1): Show | 4 | HG02129.hp2 NA19066.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3822C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635600 | ||||||
| chr5:180635601
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(241): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.59-3823T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635601 | ||||||
| chr5:180635602
|
T | A | 8 | a0001c0001t0001g0106a0001c0001t0004g0131a0001c0001t0024g0105others(5): Show | 8 | HG00639.hp1 HG02074.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3824A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635602 | ||||||
| chr5:180635602
|
T | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-3824A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635602 | ||||||
| chr5:180635602
|
T | G | 2 | a0002c0002t0001g0061a0002c0002t0001g0115 | 2 | NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3824A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635602 | ||||||
| chr5:180635604
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-3826C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635604 | ||||||
| chr5:180635604
|
G | C | 6 | a0001c0001t0001g0360a0001c0001t0002g0066a0001c0001t0002g0067others(3): Show | 6 | HG02976.hp1 HG03927.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3826C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635604 | ||||||
| chr5:180635604
|
G | T | 8 | a0001c0001t0001g0106a0001c0001t0004g0131a0001c0001t0024g0105others(5): Show | 8 | HG00639.hp1 HG02074.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3826C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635604 | ||||||
| chr5:180635605
|
A | G | 111 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0069others(108): Show | 111 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.59-3827T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635605 | ||||||
| chr5:180635606
|
T | A | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3828A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635606 | ||||||
| chr5:180635607
|
G | A | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3829C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635607 | ||||||
| chr5:180635608
|
G | A | 15 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(12): Show | 15 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3830C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635608 | ||||||
| chr5:180635608
|
G | C | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3830C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635608 | ||||||
| chr5:180635608
|
G | T | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3830C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635608 | ||||||
| chr5:180635609
|
A | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(251): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.59-3831T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635609 | ||||||
| chr5:180635610
|
T | A | 1 | a0001c0001t0005g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.59-3832A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635610 | ||||||
| chr5:180635610
|
T | C | 2 | a0001c0001t0002g0306a0004c0007t0001g0015 | 2 | HG01496.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3832A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635610 | ||||||
| chr5:180635612
|
G | T | 1 | a0001c0001t0005g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.59-3834C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635612 | ||||||
| chr5:180635613
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(178): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.59-3835T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635613 | ||||||
| chr5:180635614
|
T | A | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-3836A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635614 | ||||||
| chr5:180635616
|
G | C | 3 | a0001c0001t0001g0113a0002c0002t0001g0061a0002c0002t0001g0115 | 3 | HG01981.hp2 NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.59-3838C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635616 | ||||||
| chr5:180635616
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-3838C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635616 | ||||||
| chr5:180635617
|
A | G | 18 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0002g0116others(15): Show | 18 | HG00558.hp1 HG00639.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-3839T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635617 | ||||||
| chr5:180635618
|
T | A | 28 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(25): Show | 28 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-3840A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635618 | ||||||
| chr5:180635618
|
T | C | 5 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0002t0004g0080others(2): Show | 5 | HG03927.hp1 NA18971.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3840A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635618 | ||||||
| chr5:180635620
|
G | C | 72 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(69): Show | 72 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.59-3842C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635620 | ||||||
| chr5:180635620
|
G | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0360others(25): Show | 28 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-3842C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635620 | ||||||
| chr5:180635621
|
A | AAGTATGG others(460): Show |
1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.59-3844_59-3843ins others(467): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635621 | ||||||
| chr5:180635621
|
A | G | 13 | a0001c0001t0001g0106a0001c0001t0001g0268a0001c0001t0002g0116others(10): Show | 13 | HG00639.hp1 HG02074.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3843T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635621 | ||||||
| chr5:180635622
|
T | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.59-3844A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635622 | ||||||
| chr5:180635624
|
G | C | 2 | a0002c0002t0001g0254a0027c0042t0028g0379 | 2 | HG03195.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.59-3846C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635624 | ||||||
| chr5:180635624
|
G | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.59-3846C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635624 | ||||||
| chr5:180635625
|
A | G | 42 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0106others(39): Show | 42 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.59-3847T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635625 | ||||||
| chr5:180635626
|
T | A | 32 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(29): Show | 32 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.59-3848A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635626 | ||||||
| chr5:180635626
|
T | C | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3848A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635626 | ||||||
| chr5:180635627
|
G | T | 3 | a0001c0001t0020g0361a0002c0003t0002g0325a0002c0003t0002g0336 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.59-3849C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635627 | ||||||
| chr5:180635628
|
G | C | 1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3850C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635628 | ||||||
| chr5:180635628
|
G | T | 33 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.59-3850C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635628 | ||||||
| chr5:180635629
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(163): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.59-3851T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635629 | ||||||
| chr5:180635630
|
T | A | 15 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0128others(12): Show | 15 | HG00741.hp2 HG01981.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3852A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635630 | ||||||
| chr5:180635632
|
G | T | 15 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0128others(12): Show | 15 | HG00741.hp2 HG01981.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3854C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635632 | ||||||
| chr5:180635633
|
A | G | 66 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0069others(63): Show | 66 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.59-3855T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635633 | ||||||
| chr5:180635634
|
T | A | 71 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(68): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.59-3856A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635634 | ||||||
| chr5:180635636
|
G | C | 2 | a0002c0002t0004g0033a0002c0003t0003g0274 | 2 | HG02129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.59-3858C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635636 | ||||||
| chr5:180635636
|
G | T | 71 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(68): Show | 71 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.59-3858C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635636 | ||||||
| chr5:180635637
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(184): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.59-3859T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635637 | ||||||
| chr5:180635638
|
T | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3860A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635638 | ||||||
| chr5:180635640
|
G | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0365a0001c0001t0002g0107others(9): Show | 12 | HG00639.hp1 HG00673.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3862C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635640 | ||||||
| chr5:180635640
|
G | T | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3862C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635640 | ||||||
| chr5:180635641
|
A | ATGGGTGG others(808): Show |
1 | a0002c0029t0001g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.59-3864_59-3863ins others(815): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635641 | ||||||
| chr5:180635641
|
A | G | 132 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.59-3863T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635641 | ||||||
| chr5:180635641
|
A | T | 1 | a0030c0050t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.59-3863T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635641 | ||||||
| chr5:180635642
|
T | A | 3 | a0005c0018t0013g0167a0025c0037t0001g0249a0030c0050t0001g0112 | 3 | HG01168.hp1 HG02257.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.59-3864A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635642 | ||||||
| chr5:180635644
|
G | C | 4 | a0001c0001t0001g0268a0001c0001t0002g0297a0002c0003t0003g0298others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-3866C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635644 | ||||||
| chr5:180635644
|
G | T | 2 | a0005c0018t0013g0167a0025c0037t0001g0249 | 2 | HG01168.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.59-3866C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635644 | ||||||
| chr5:180635645
|
A | AAGTAAGG others(225): Show |
1 | a0002c0002t0004g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3868_59-3867ins others(232): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635645 | ||||||
| chr5:180635645
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(194): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.59-3867T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635645 | ||||||
| chr5:180635646
|
T | A | 1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3868A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635646 | ||||||
| chr5:180635648
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3870C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635648 | ||||||
| chr5:180635648
|
G | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-3870C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635648 | ||||||
| chr5:180635648
|
G | T | 1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3870C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635648 | ||||||
| chr5:180635649
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(272): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.59-3871T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635649 | ||||||
| chr5:180635650
|
T | A | 15 | a0001c0001t0001g0106a0001c0001t0001g0365a0001c0001t0002g0107others(12): Show | 15 | HG00639.hp1 HG00673.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-3872A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635650 | ||||||
| chr5:180635651
|
G | A | 33 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(30): Show | 33 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.59-3873C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635651 | ||||||
| chr5:180635652
|
G | A | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-3874C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635652 | ||||||
| chr5:180635652
|
G | T | 14 | a0001c0001t0001g0106a0001c0001t0001g0365a0001c0001t0002g0107others(11): Show | 14 | HG00639.hp1 HG00673.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-3874C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635652 | ||||||
| chr5:180635653
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(256): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.59-3875T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635653 | ||||||
| chr5:180635653
|
AT | A | 33 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0091others(30): Show | 33 | HG00099.hp1 HG00423.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.59-3876delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635653 | ||||||
| chr5:180635654
|
T | A | 23 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-3876A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635654 | ||||||
| chr5:180635654
|
T | TGAGA | 11 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0004g0142others(8): Show | 11 | HG00741.hp2 HG02015.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-3877_59-3876ins others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635654 | ||||||
| chr5:180635656
|
G | C | 3 | a0001c0001t0002g0306a0001c0001t0005g0079a0004c0007t0001g0015 | 3 | HG01496.hp2 NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3878C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635656 | ||||||
| chr5:180635657
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(192): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.59-3879T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635657 | ||||||
| chr5:180635658
|
T | A | 5 | a0001c0001t0001g0268a0001c0001t0001g0360a0001c0001t0002g0297others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3880A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635658 | ||||||
| chr5:180635660
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3882C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635660 | ||||||
| chr5:180635660
|
G | T | 5 | a0001c0001t0001g0268a0001c0001t0001g0360a0001c0001t0002g0297others(2): Show | 5 | HG01891.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3882C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635660 | ||||||
| chr5:180635661
|
A | AAGTATGG others(577): Show |
1 | a0001c0001t0001g0309 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(584): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(569): Show |
2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59-3884_59-3883ins others(576): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(593): Show |
1 | a0002c0002t0014g0031 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(600): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(697): Show |
18 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(15): Show | 18 | HG00280.hp1 HG01123.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-3884_59-3883ins others(704): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(641): Show |
1 | a0002c0002t0004g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(648): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(629): Show |
1 | a0003c0005t0001g0058 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(636): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(625): Show |
1 | a0008c0025t0017g0009 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(632): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(569): Show |
2 | a0003c0005t0002g0042a0019c0040t0002g0046 | 2 | HG00642.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.59-3884_59-3883ins others(576): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(629): Show |
37 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0002g0047others(34): Show | 37 | HG00099.hp2 HG00408.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.59-3884_59-3883ins others(636): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(689): Show |
1 | a0002c0003t0010g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(696): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(613): Show |
1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(620): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | AAGTATGG others(629): Show |
1 | a0001c0023t0008g0377 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.59-3884_59-3883ins others(636): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | ATGCATGG others(796): Show |
6 | a0001c0047t0001g0173a0002c0003t0001g0375a0002c0022t0003g0147others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3884_59-3883ins others(803): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635661
|
A | G | 33 | a0001c0001t0001g0113a0001c0001t0002g0066a0001c0001t0002g0067others(30): Show | 33 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.59-3883T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635661 | ||||||
| chr5:180635662
|
T | A | 8 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3884A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635662 | ||||||
| chr5:180635662
|
T | C | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3884A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635662 | ||||||
| chr5:180635662
|
T | G | 13 | a0001c0001t0001g0309a0001c0001t0002g0066a0001c0001t0002g0067others(10): Show | 13 | HG00642.hp1 HG02145.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3884A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635662 | ||||||
| chr5:180635663
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-3885C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635663 | ||||||
| chr5:180635664
|
G | C | 72 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.59-3886C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635664 | ||||||
| chr5:180635664
|
G | T | 8 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3886C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635664 | ||||||
| chr5:180635665
|
A | G | 39 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0001g0268others(36): Show | 39 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.59-3887T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635665 | ||||||
| chr5:180635667
|
G | A | 15 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(12): Show | 15 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-3889C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635667 | ||||||
| chr5:180635668
|
G | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(144): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.59-3890C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635668 | ||||||
| chr5:180635669
|
A | AAGTATGG others(652): Show |
1 | a0004c0007t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.59-3892_59-3891ins others(659): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635669 | ||||||
| chr5:180635669
|
A | G | 26 | a0001c0001t0002g0116a0001c0001t0002g0177a0001c0001t0002g0229others(23): Show | 26 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-3891T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635669 | ||||||
| chr5:180635670
|
T | A | 2 | a0001c0001t0002g0306a0001c0001t0005g0079 | 2 | NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3892A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635670 | ||||||
| chr5:180635672
|
G | C | 4 | a0001c0001t0002g0273a0001c0001t0006g0122a0001c0001t0006g0209others(1): Show | 4 | HG03669.hp2 NA18612.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3894C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635672 | ||||||
| chr5:180635672
|
G | T | 2 | a0001c0001t0002g0306a0001c0001t0005g0079 | 2 | NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3894C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635672 | ||||||
| chr5:180635673
|
A | G | 8 | a0001c0001t0001g0268a0001c0001t0001g0360a0001c0001t0002g0116others(5): Show | 8 | HG01891.hp2 HG02129.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3895T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635673 | ||||||
| chr5:180635675
|
G | A | 1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3897C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635675 | ||||||
| chr5:180635676
|
G | A | 1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3898C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635676 | ||||||
| chr5:180635676
|
G | C | 88 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.59-3898C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635676 | ||||||
| chr5:180635677
|
A | AAGTATGG others(689): Show |
1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-3900_59-3899ins others(696): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635677 | ||||||
| chr5:180635677
|
A | ATGAAGTA others(734): Show |
1 | a0007c0010t0015g0252 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.59-3900_59-3899ins others(741): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635677 | ||||||
| chr5:180635677
|
A | G | 17 | a0001c0001t0001g0268a0001c0001t0002g0116a0001c0001t0002g0297others(14): Show | 17 | HG01891.hp2 HG02129.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-3899T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635677 | ||||||
| chr5:180635678
|
T | C | 70 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(67): Show | 70 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-3900A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635678 | ||||||
| chr5:180635680
|
G | C | 16 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(13): Show | 16 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3902C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635680 | ||||||
| chr5:180635681
|
A | G | 1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3903T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635681 | ||||||
| chr5:180635682
|
T | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(143): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-3904A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635682 | ||||||
| chr5:180635682
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-3904A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635682 | ||||||
| chr5:180635684
|
G | C | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3906C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635684 | ||||||
| chr5:180635684
|
G | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(143): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-3906C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635684 | ||||||
| chr5:180635685
|
A | G | 10 | a0001c0001t0002g0306a0001c0001t0002g0371a0001c0001t0002g0372others(7): Show | 10 | HG02647.hp2 HG02809.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-3907T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635685 | ||||||
| chr5:180635686
|
T | A | 178 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.59-3908A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635686 | ||||||
| chr5:180635687
|
G | T | 16 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(13): Show | 16 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3909C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635687 | ||||||
| chr5:180635688
|
T | C | 5 | a0001c0001t0002g0116a0001c0001t0006g0051a0002c0003t0003g0274others(2): Show | 5 | HG02129.hp2 HG03195.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3910A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635688 | ||||||
| chr5:180635688
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(171): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.59-3910A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635688 | ||||||
| chr5:180635689
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(153): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.59-3911T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635689 | ||||||
| chr5:180635690
|
T | A | 16 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(13): Show | 16 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3912A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635690 | ||||||
| chr5:180635692
|
G | GGTGGATG others(744): Show |
1 | a0001c0001t0006g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-3915_59-3914ins others(751): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635692 | ||||||
| chr5:180635692
|
G | GGTGGATG others(744): Show |
1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-3915_59-3914ins others(751): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635692 | ||||||
| chr5:180635692
|
G | T | 16 | a0001c0001t0002g0177a0001c0001t0002g0229a0001c0001t0002g0253others(13): Show | 16 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-3914C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635692 | ||||||
| chr5:180635693
|
A | G | 184 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.59-3915T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635693 | ||||||
| chr5:180635694
|
T | C | 2 | a0001c0001t0002g0306a0001c0001t0005g0079 | 2 | NA18982.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.59-3916A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635694 | ||||||
| chr5:180635695
|
G | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-3917C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635695 | ||||||
| chr5:180635696
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-3918C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635696 | ||||||
| chr5:180635697
|
A | AAGTATGG others(716): Show |
1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-3920_59-3919ins others(723): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635697 | ||||||
| chr5:180635697
|
A | ATGGAAGT others(61): Show |
1 | a0002c0003t0003g0274 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-3920_59-3919ins others(68): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635697 | ||||||
| chr5:180635697
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(171): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.59-3919T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635697 | ||||||
| chr5:180635698
|
T | A | 2 | a0001c0001t0001g0360a0001c0001t0002g0116 | 2 | HG02976.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.59-3920A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635698 | ||||||
| chr5:180635700
|
G | T | 2 | a0001c0001t0001g0360a0001c0001t0002g0116 | 2 | HG02976.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.59-3922C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635700 | ||||||
| chr5:180635701
|
A | G | 322 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(319): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.59-3923T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635701 | ||||||
| chr5:180635705
|
A | G | 41 | a0001c0001t0001g0106a0001c0001t0001g0268a0001c0001t0001g0360others(38): Show | 41 | HG00323.hp2 HG00673.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.59-3927T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635705 | ||||||
| chr5:180635706
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(143): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-3928A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635706 | ||||||
| chr5:180635708
|
G | C | 8 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3930C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635708 | ||||||
| chr5:180635709
|
A | AAGTATGG others(728): Show |
1 | a0001c0001t0005g0079 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.59-3932_59-3931ins others(735): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635709 | ||||||
| chr5:180635709
|
A | G | 200 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.59-3931T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635709 | ||||||
| chr5:180635710
|
T | A | 1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3932A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635710 | ||||||
| chr5:180635711
|
G | GTATGGGT others(704): Show |
1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-3934_59-3933ins others(711): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635711 | ||||||
| chr5:180635712
|
G | A | 20 | a0001c0001t0001g0106a0001c0001t0001g0356a0001c0001t0002g0107others(17): Show | 21 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-3934C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635712 | ||||||
| chr5:180635713
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(151): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.59-3935C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635713 | ||||||
| chr5:180635713
|
GTGGATGG others(5): Show |
G | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-3947_59-3936del others(12): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635713 | ||||||
| chr5:180635714
|
T | A | 20 | a0001c0001t0001g0106a0001c0001t0001g0356a0001c0001t0002g0107others(17): Show | 21 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-3936A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635714 | ||||||
| chr5:180635717
|
A | G | 191 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.59-3939T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635717 | ||||||
| chr5:180635721
|
A | AAGTATGG others(881): Show |
2 | a0001c0001t0010g0368a0002c0003t0001g0370 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.59-3944_59-3943ins others(888): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(885): Show |
6 | a0001c0001t0002g0371a0001c0001t0002g0372a0002c0003t0001g0317others(3): Show | 6 | HG02809.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3944_59-3943ins others(892): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(688): Show |
1 | a0014c0020t0007g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(695): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(741): Show |
1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(748): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(740): Show |
1 | a0014c0020t0013g0271 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(747): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(728): Show |
1 | a0001c0001t0001g0272 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(735): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(740): Show |
133 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(130): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.59-3944_59-3943ins others(747): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(740): Show |
1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(747): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(684): Show |
1 | a0002c0003t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(691): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | AAGTATGG others(788): Show |
7 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 7 | HG02258.hp2 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3944_59-3943ins others(795): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | ATGCATGG others(441): Show |
1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(448): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | ATGCATGG others(149): Show |
1 | a0001c0001t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(156): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | ATGCATGG others(253): Show |
1 | a0002c0002t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(260): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | ATGCATGG others(1596): Show |
1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.59-3944_59-3943ins others(1603): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635721
|
A | G | 188 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.59-3943T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635721 | ||||||
| chr5:180635722
|
T | C | 1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3944A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635722 | ||||||
| chr5:180635722
|
T | G | 128 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0038others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.59-3944A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635722 | ||||||
| chr5:180635724
|
G | C | 22 | a0001c0001t0001g0106a0001c0001t0001g0356a0001c0001t0002g0107others(19): Show | 23 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-3946C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635724 | ||||||
| chr5:180635732
|
G | C | 3 | a0001c0001t0002g0297a0002c0003t0003g0298a0005c0018t0011g0041 | 3 | HG01891.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3954C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635732 | ||||||
| chr5:180635736
|
G | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.59-3958C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635736 | ||||||
| chr5:180635738
|
T | A | 2 | a0001c0001t0001g0360a0001c0001t0006g0051 | 2 | HG02976.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.59-3960A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635738 | ||||||
| chr5:180635738
|
T | C | 22 | a0001c0001t0001g0106a0001c0001t0001g0356a0001c0001t0002g0107others(19): Show | 23 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-3960A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635738 | ||||||
| chr5:180635740
|
G | T | 2 | a0001c0001t0001g0360a0001c0001t0006g0051 | 2 | HG02976.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.59-3962C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635740 | ||||||
| chr5:180635745
|
A | G | 2 | a0001c0001t0001g0360a0001c0001t0006g0051 | 2 | HG02976.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.59-3967T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635745 | ||||||
| chr5:180635746
|
T | A | 368 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(365): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.59-3968A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635746 | ||||||
| chr5:180635748
|
G | T | 368 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(365): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.59-3970C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635748 | ||||||
| chr5:180635750
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(146): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.59-3972A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635750 | ||||||
| chr5:180635750
|
T | TGGGTGGA others(700): Show |
1 | a0002c0003t0003g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-3973_59-3972ins others(707): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635750 | ||||||
| chr5:180635750
|
T | TGGGTGGA others(804): Show |
2 | a0001c0001t0002g0297a0005c0018t0011g0041 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-3973_59-3972ins others(811): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635750 | ||||||
| chr5:180635755
|
G | C | 46 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.59-3977C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635755 | ||||||
| chr5:180635756
|
G | A | 46 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0309others(43): Show | 46 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.59-3978C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635756 | ||||||
| chr5:180635756
|
G | GGTGGGTG others(733): Show |
1 | a0001c0001t0006g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.59-3979_59-3978ins others(740): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635756 | ||||||
| chr5:180635756
|
G | GGTGGGTG others(756): Show |
1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3979_59-3978ins others(763): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635756 | ||||||
| chr5:180635761
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(366): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.59-3983T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635761 | ||||||
| chr5:180635768
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3990C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635768 | ||||||
| chr5:180635773
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-3995C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635773 | ||||||
| chr5:180635782
|
T | G | 372 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(369): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.59-4004A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635782 | ||||||
| chr5:180635785
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-4007T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635785 | ||||||
| chr5:180635792
|
G | C | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-4014C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635792 | ||||||
| chr5:180635795
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-4017C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635795 | ||||||
| chr5:180635796
|
C | G | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-4018G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635796 | ||||||
| chr5:180635808
|
T | TATGGGTC others(1): Show |
325 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(322): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.59-4031_59-4030ins others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635808 | ||||||
| chr5:180635815
|
G | C | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-4037C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635815 | ||||||
| chr5:180635816
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-4038C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635816 | ||||||
| chr5:180635817
|
A | G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4039T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635817 | ||||||
| chr5:180635825
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-4047C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635825 | ||||||
| chr5:180635844
|
CATGGATG others(25): Show |
C | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4098_59-4067del others(32): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635844 | ||||||
| chr5:180635850
|
T | G | 2 | a0002c0002t0018g0109a0002c0002t0018g0163 | 2 | NA18950.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.59-4072A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635850 | ||||||
| chr5:180635882
|
T | A | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-4104A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635882 | ||||||
| chr5:180635884
|
G | T | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-4106C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635884 | ||||||
| chr5:180635886
|
T | C | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4108A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635886 | ||||||
| chr5:180635889
|
G | A | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4111C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635889 | ||||||
| chr5:180635890
|
A | T | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-4112T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635890 | ||||||
| chr5:180635892
|
T | G | 1 | a0023c0036t0001g0110 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.59-4114A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635892 | ||||||
| chr5:180635901
|
ATGGG | A | 3 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0218 | 3 | NA18941.hp2 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.59-4127_59-4124del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635901 | ||||||
| chr5:180635909
|
G | A | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4131C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635909 | ||||||
| chr5:180635914
|
T | G | 1 | a0001c0001t0002g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-4136A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635914 | ||||||
| chr5:180635921
|
A | G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4143T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635921 | ||||||
| chr5:180635925
|
A | G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4147T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635925 | ||||||
| chr5:180635934
|
C | T | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4156G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635934 | ||||||
| chr5:180635934
|
CGGATGGA others(61): Show |
C | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.59-4224_59-4157del others(68): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635934 | ||||||
| chr5:180635935
|
G | A | 2 | a0001c0001t0002g0229a0001c0043t0002g0230 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.59-4157C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635935 | ||||||
| chr5:180635953
|
A | G | 25 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(22): Show | 25 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-4175T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635953 | ||||||
| chr5:180635961
|
GTGGGTGG others(9): Show |
G | 1 | a0002c0004t0005g0285 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-4199_59-4184del others(16): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180635961 | ||||||
| chr5:180636013
|
A | G | 1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-4235T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636013 | ||||||
| chr5:180636020
|
G | A | 1 | a0001c0001t0002g0275 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-4242C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636020 | ||||||
| chr5:180636100
|
G | A | 1 | a0002c0003t0002g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-4322C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636100 | ||||||
| chr5:180636178
|
C | G | 1 | a0002c0041t0005g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59-4400G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636178 | ||||||
| chr5:180636327
|
CTTATGTG others(37): Show |
C | 1 | a0001c0006t0001g0154 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.59-4593_59-4550del others(44): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636327 | ||||||
| chr5:180636428
|
A | G | 1 | a0024c0046t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.59-4650T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636428 | ||||||
| chr5:180636458
|
C | T | 1 | a0002c0004t0005g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.59-4680G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636458 | ||||||
| chr5:180636558
|
C | A | 10 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(7): Show | 10 | HG02257.hp2 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-4780G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636558 | ||||||
| chr5:180636593
|
T | A | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-4815A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636593 | ||||||
| chr5:180636614
|
C | G | 3 | a0001c0001t0001g0330a0012c0017t0001g0328a0012c0017t0001g0329 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.59-4836G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636614 | ||||||
| chr5:180636686
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.59-4908C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636686 | ||||||
| chr5:180636743
|
C | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.59-4965G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636743 | ||||||
| chr5:180636805
|
T | G | 11 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0197others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-5027A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636805 | ||||||
| chr5:180636823
|
T | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(331): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.59-5045A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636823 | ||||||
| chr5:180636952
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-5174C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180636952 | ||||||
| chr5:180637016
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-5238G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637016 | ||||||
| chr5:180637017
|
T | C | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-5239A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637017 | ||||||
| chr5:180637018
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-5240G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637018 | ||||||
| chr5:180637204
|
C | G | 1 | a0001c0001t0002g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.59-5426G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637204 | ||||||
| chr5:180637223
|
G | A | 1 | a0001c0032t0026g0333 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-5445C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637223 | ||||||
| chr5:180637244
|
C | T | 2 | a0005c0018t0013g0167a0027c0042t0028g0379 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.59-5466G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637244 | ||||||
| chr5:180637294
|
C | T | 334 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(331): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.59-5516G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637294 | ||||||
| chr5:180637330
|
G | GA | 14 | a0001c0001t0001g0038a0001c0001t0002g0371a0001c0001t0002g0372others(11): Show | 14 | HG01928.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.59-5553dupT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637330 | ||||||
| chr5:180637330
|
GA | G | 154 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0062others(151): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.59-5553delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637330 | ||||||
| chr5:180637366
|
T | C | 69 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.59-5588A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637366 | ||||||
| chr5:180637458
|
C | T | 1 | a0013c0019t0008g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-5680G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637458 | ||||||
| chr5:180637494
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(333): Show | 344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.59-5716T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637494 | ||||||
| chr5:180637501
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG03017.hp2 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.59-5723T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637501 | ||||||
| chr5:180637681
|
C | T | 1 | a0013c0019t0008g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.59-5903G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637681 | ||||||
| chr5:180637693
|
C | T | 6 | a0002c0003t0010g0043a0002c0003t0010g0178a0002c0012t0001g0052others(3): Show | 6 | HG02451.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-5915G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637693 | ||||||
| chr5:180637993
|
C | T | 1 | a0001c0001t0006g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.59-6215G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180637993 | ||||||
| chr5:180638103
|
C | T | 334 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(331): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.59-6325G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638103 | ||||||
| chr5:180638139
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.59-6361C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638139 | ||||||
| chr5:180638270
|
C | T | 1 | a0025c0037t0001g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.59-6492G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638270 | ||||||
| chr5:180638296
|
C | G | 1 | a0001c0001t0002g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-6518G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638296 | ||||||
| chr5:180638455
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(145): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.59-6677T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638455 | ||||||
| chr5:180638531
|
T | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0216others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-6753A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638531 | ||||||
| chr5:180638697
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(139): Show | 149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.59-6919A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638697 | ||||||
| chr5:180638702
|
T | G | 1 | a0002c0002t0001g0084 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.59-6924A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638702 | ||||||
| chr5:180638705
|
C | CCCCAGGC others(37): Show |
1 | a0001c0006t0001g0154 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.59-6928_59-6927ins others(44): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638705 | ||||||
| chr5:180638745
|
C | A | 1 | a0018c0039t0001g0040 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59-6967G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638745 | ||||||
| chr5:180638884
|
A | G | 1 | a0002c0002t0001g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.59-7106T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638884 | ||||||
| chr5:180638977
|
C | T | 10 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(7): Show | 10 | HG00323.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-7199G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180638977 | ||||||
| chr5:180639098
|
CATGGATG others(137): Show |
C | 60 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0062others(57): Show | 60 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-7464_59-7321del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639098 | ||||||
| chr5:180639171
|
ATGGATGG others(113): Show |
A | 1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-7513_59-7394del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639171 | ||||||
| chr5:180639178
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7400C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639178 | ||||||
| chr5:180639179
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7401C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639179 | ||||||
| chr5:180639189
|
GGACA | G | 8 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-7415_59-7412del others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639189 | ||||||
| chr5:180639195
|
A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7417T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639195 | ||||||
| chr5:180639196
|
C | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7418G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639196 | ||||||
| chr5:180639203
|
A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7425T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639203 | ||||||
| chr5:180639208
|
T | A | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-7430A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639208 | ||||||
| chr5:180639209
|
G | T | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-7431C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639209 | ||||||
| chr5:180639210
|
GATGGACA others(153): Show |
G | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0215others(20): Show | 23 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-7592_59-7433del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639210 | ||||||
| chr5:180639227
|
GTGGATGG others(153): Show |
G | 2 | a0002c0003t0001g0003a0002c0003t0001g0243 | 3 | HG01515.hp1 HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.59-7609_59-7450del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639227 | ||||||
| chr5:180639234
|
GGTGGACG others(129): Show |
G | 203 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(200): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.59-7592_59-7457del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639234 | ||||||
| chr5:180639235
|
GTGGACGG others(141): Show |
G | 1 | a0001c0001t0001g0244 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.59-7605_59-7458del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639235 | ||||||
| chr5:180639239
|
ACGGATGG others(125): Show |
A | 3 | a0001c0001t0001g0277a0001c0001t0001g0299a0001c0001t0002g0300 | 3 | HG02622.hp2 HG02922.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.59-7593_59-7462del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639239 | ||||||
| chr5:180639239
|
ACGGATGG others(133): Show |
A | 60 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0001g0129others(57): Show | 62 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.59-7601_59-7462del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639239 | ||||||
| chr5:180639240
|
C | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-7462G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639240 | ||||||
| chr5:180639241
|
GGATGGAT others(128): Show |
G | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.59-7598_59-7464del | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639241 | ||||||
| chr5:180639317
|
GGATGGGT others(17): Show |
G | 1 | a0002c0002t0004g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-7563_59-7540del others(24): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639317 | ||||||
| chr5:180639375
|
A | ATGGG | 3 | a0001c0001t0002g0371a0001c0001t0002g0372a0002c0003t0007g0373 | 3 | HG02965.hp2 HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.59-7601_59-7598dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639375 | ||||||
| chr5:180639379
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(227): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.59-7601C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639379 | ||||||
| chr5:180639379
|
G | GTGGA | 4 | a0002c0003t0001g0317a0002c0012t0021g0174a0005c0018t0013g0167others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-7605_59-7602dup others(4): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639379 | ||||||
| chr5:180639379
|
G | GTGGATGG others(1): Show |
3 | a0001c0001t0010g0368a0002c0002t0004g0032a0002c0003t0001g0370 | 3 | HG02647.hp2 HG02735.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.59-7609_59-7602dup others(8): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639379 | ||||||
| chr5:180639400
|
C | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(330): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.59-7622G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639400 | ||||||
| chr5:180639447
|
A | G | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-7669T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639447 | ||||||
| chr5:180639475
|
G | T | 2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.59-7697C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639475 | ||||||
| chr5:180639481
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0222a0001c0001t0001g0293others(2): Show | 7 | HG01074.hp1 HG01099.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-7703G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639481 | ||||||
| chr5:180639547
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(309): Show | 320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.59-7769T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180639547 | ||||||
| chr5:180640045
|
C | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0002g0306others(17): Show | 20 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-8267G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640045 | ||||||
| chr5:180640051
|
C | G | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-8273G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640051 | ||||||
| chr5:180640054
|
G | C | 1 | a0002c0002t0001g0115 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.59-8276C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640054 | ||||||
| chr5:180640088
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(291): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.59-8310C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640088 | ||||||
| chr5:180640092
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-8314C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640092 | ||||||
| chr5:180640183
|
G | T | 3 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.59-8405C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640183 | ||||||
| chr5:180640414
|
C | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(310): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.59-8636G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640414 | ||||||
| chr5:180640433
|
G | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0022others(311): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.59-8655C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640433 | ||||||
| chr5:180640675
|
G | A | 52 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.58+8813C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640675 | ||||||
| chr5:180640727
|
G | A | 26 | a0001c0001t0001g0062a0001c0006t0001g0154a0001c0006t0001g0157others(23): Show | 26 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.58+8761C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640727 | ||||||
| chr5:180640751
|
G | A | 3 | a0001c0001t0001g0356a0001c0001t0012g0357a0001c0001t0012g0358 | 3 | HG00280.hp2 HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.58+8737C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640751 | ||||||
| chr5:180640870
|
C | T | 3 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.58+8618G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640870 | ||||||
| chr5:180640890
|
T | C | 2 | a0002c0002t0001g0027a0002c0003t0007g0315 | 2 | HG00099.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58+8598A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640890 | ||||||
| chr5:180640968
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0020others(312): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.58+8520A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180640968 | ||||||
| chr5:180641009
|
T | C | 35 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(32): Show | 36 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.58+8479A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641009 | ||||||
| chr5:180641154
|
C | T | 88 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.58+8334G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641154 | ||||||
| chr5:180641155
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.58+8333C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641155 | ||||||
| chr5:180641239
|
A | T | 160 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0025others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.58+8249T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641239 | ||||||
| chr5:180641279
|
T | C | 16 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0002g0290others(13): Show | 16 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+8209A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641279 | ||||||
| chr5:180641419
|
G | C | 1 | a0001c0001t0002g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+8069C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641419 | ||||||
| chr5:180641448
|
C | G | 1 | a0003c0005t0002g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.58+8040G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641448 | ||||||
| chr5:180641571
|
G | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7917C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641571 | ||||||
| chr5:180641597
|
C | CCT | 67 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0057others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.58+7889_58+7890dup others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641597 | ||||||
| chr5:180641637
|
G | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7851C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641637 | ||||||
| chr5:180641702
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7786A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641702 | ||||||
| chr5:180641741
|
G | A | 57 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(54): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.58+7747C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641741 | ||||||
| chr5:180641767
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7721A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641767 | ||||||
| chr5:180641769
|
C | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7719G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641769 | ||||||
| chr5:180641771
|
C | T | 5 | a0002c0002t0001g0351a0002c0002t0001g0352a0002c0002t0001g0353others(2): Show | 5 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+7717G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641771 | ||||||
| chr5:180641796
|
C | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7692G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641796 | ||||||
| chr5:180641935
|
A | G | 178 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(175): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.58+7553T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641935 | ||||||
| chr5:180641957
|
A | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(50): Show | 55 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.58+7531T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641957 | ||||||
| chr5:180641983
|
C | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7505G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641983 | ||||||
| chr5:180641990
|
G | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7498C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641990 | ||||||
| chr5:180641990
|
G | T | 1 | a0002c0002t0001g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.58+7498C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641990 | ||||||
| chr5:180641996
|
CAA | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7490_58+7491del others(2): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641996 | ||||||
| chr5:180641998
|
A | G | 2 | a0001c0001t0020g0361a0002c0002t0001g0002 | 3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.58+7490T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180641998 | ||||||
| chr5:180642004
|
T | C | 2 | a0001c0001t0020g0361a0002c0002t0001g0002 | 3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.58+7484A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642004 | ||||||
| chr5:180642012
|
T | C | 4 | a0002c0002t0001g0345a0002c0002t0001g0346a0002c0002t0001g0347others(1): Show | 4 | HG00639.hp1 HG00642.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7476A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642012 | ||||||
| chr5:180642012
|
T | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0222a0001c0001t0001g0293others(4): Show | 9 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+7476A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642012 | ||||||
| chr5:180642019
|
C | T | 8 | a0001c0001t0001g0225a0001c0001t0001g0365a0001c0001t0012g0005others(5): Show | 9 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+7469G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642019 | ||||||
| chr5:180642024
|
T | C | 13 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(10): Show | 13 | HG01167.hp1 HG02647.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+7464A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642024 | ||||||
| chr5:180642036
|
A | G | 2 | a0001c0001t0001g0224a0002c0038t0004g0068 | 2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.58+7452T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642036 | ||||||
| chr5:180642124
|
G | A | 192 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0038others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.58+7364C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642124 | ||||||
| chr5:180642124
|
G | GTGAACCT others(42): Show |
1 | a0001c0001t0001g0367 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.58+7363_58+7364ins others(49): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642124 | ||||||
| chr5:180642131
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7357A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642131 | ||||||
| chr5:180642148
|
A | G | 1 | a0002c0003t0005g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+7340T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642148 | ||||||
| chr5:180642152
|
G | A | 3 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.58+7336C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642152 | ||||||
| chr5:180642163
|
C | T | 2 | a0001c0001t0002g0082a0003c0005t0001g0034 | 2 | HG01123.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.58+7325G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642163 | ||||||
| chr5:180642186
|
G | A | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+7302C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642186 | ||||||
| chr5:180642206
|
G | GA | 8 | a0002c0002t0001g0211a0002c0003t0003g0074a0002c0003t0003g0132others(5): Show | 9 | HG00140.hp2 HG00733.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+7281dupT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642206 | ||||||
| chr5:180642206
|
GA | G | 21 | a0001c0001t0001g0057a0001c0001t0001g0222a0001c0001t0012g0223others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.58+7281delT | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642206 | ||||||
| chr5:180642392
|
G | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7096C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642392 | ||||||
| chr5:180642410
|
C | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+7078G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642410 | ||||||
| chr5:180642604
|
T | A | 1 | a0002c0012t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58+6884A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642604 | ||||||
| chr5:180642648
|
G | C | 52 | a0001c0001t0001g0309a0001c0001t0001g0330a0001c0001t0001g0356others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.58+6840C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642648 | ||||||
| chr5:180642705
|
C | T | 1 | a0002c0002t0003g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58+6783G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642705 | ||||||
| chr5:180642726
|
C | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6762G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642726 | ||||||
| chr5:180642764
|
A | G | 1 | a0002c0035t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+6724T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642764 | ||||||
| chr5:180642827
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58+6661G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642827 | ||||||
| chr5:180642852
|
T | C | 52 | a0001c0001t0001g0309a0001c0001t0001g0330a0001c0001t0001g0356others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.58+6636A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642852 | ||||||
| chr5:180642884
|
G | A | 1 | a0010c0021t0001g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.58+6604C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642884 | ||||||
| chr5:180642933
|
A | G | 22 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0002g0067others(19): Show | 22 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+6555T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642933 | ||||||
| chr5:180642971
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6517A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642971 | ||||||
| chr5:180642995
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6493T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180642995 | ||||||
| chr5:180643025
|
C | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6463G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643025 | ||||||
| chr5:180643076
|
T | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6412A>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643076 | ||||||
| chr5:180643128
|
A | G | 22 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0002g0067others(19): Show | 22 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+6360T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643128 | ||||||
| chr5:180643155
|
C | A | 113 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0057others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.58+6333G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643155 | ||||||
| chr5:180643295
|
G | A | 2 | a0002c0004t0005g0053a0002c0004t0005g0054 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.58+6193C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643295 | ||||||
| chr5:180643296
|
C | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6192G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643296 | ||||||
| chr5:180643297
|
G | A | 52 | a0001c0001t0001g0309a0001c0001t0001g0330a0001c0001t0001g0356others(49): Show | 53 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.58+6191C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643297 | ||||||
| chr5:180643316
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6172A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643316 | ||||||
| chr5:180643376
|
A | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6112T>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643376 | ||||||
| chr5:180643406
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6082T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643406 | ||||||
| chr5:180643430
|
C | T | 7 | a0002c0002t0001g0211a0004c0007t0001g0185a0004c0007t0001g0210others(4): Show | 8 | HG00140.hp2 HG00733.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6058G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643430 | ||||||
| chr5:180643481
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6007T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643481 | ||||||
| chr5:180643489
|
TC | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0133a0001c0009t0001g0063others(11): Show | 14 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.58+5998delG | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643489 | ||||||
| chr5:180643563
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5925T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643563 | ||||||
| chr5:180643825
|
G | GT | 17 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0004g0078others(14): Show | 17 | HG00423.hp2 HG00741.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+5662dupA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643825 | ||||||
| chr5:180643825
|
GT | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0135others(10): Show | 13 | HG01168.hp2 HG02165.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5662delA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643825 | ||||||
| chr5:180643842
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5646T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643842 | ||||||
| chr5:180643852
|
C | T | 5 | a0002c0002t0001g0351a0002c0002t0001g0352a0002c0002t0001g0353others(2): Show | 5 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5636G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643852 | ||||||
| chr5:180643884
|
C | G | 17 | a0001c0001t0001g0057a0001c0001t0001g0215a0001c0001t0002g0216others(14): Show | 17 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+5604G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643884 | ||||||
| chr5:180643924
|
C | T | 121 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(118): Show | 122 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.58+5564G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180643924 | ||||||
| chr5:180644064
|
G | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5424C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644064 | ||||||
| chr5:180644096
|
C | T | 12 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(9): Show | 12 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+5392G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644096 | ||||||
| chr5:180644107
|
A | G | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5381T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644107 | ||||||
| chr5:180644114
|
G | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5374C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644114 | ||||||
| chr5:180644116
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5372A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644116 | ||||||
| chr5:180644122
|
C | T | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5366G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644122 | ||||||
| chr5:180644163
|
G | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+5325C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644163 | ||||||
| chr5:180644208
|
TGGCTGGT others(45): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58+5228_58+5279del others(52): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644208 | ||||||
| chr5:180644249
|
T | A | 101 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0062others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.58+5239A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644249 | ||||||
| chr5:180644270
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.58+5218C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644270 | ||||||
| chr5:180644276
|
G | A | 111 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(108): Show | 111 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.58+5212C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644276 | ||||||
| chr5:180644292
|
G | A | 2 | a0001c0001t0004g0142a0002c0003t0003g0143 | 2 | HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.58+5196C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644292 | ||||||
| chr5:180644336
|
C | T | 1 | a0001c0001t0006g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+5152G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644336 | ||||||
| chr5:180644663
|
A | ACCTGTAC others(46): Show |
1 | a0001c0001t0001g0038 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58+4772_58+4824dup others(53): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644663 | ||||||
| chr5:180644695
|
G | T | 2 | a0001c0001t0002g0371a0001c0001t0002g0372 | 2 | HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.58+4793C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644695 | ||||||
| chr5:180644709
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.58+4779G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644709 | ||||||
| chr5:180644728
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0002c0002t0001g0072others(2): Show | 5 | NA18612.hp2 NA18951.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+4760G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644728 | ||||||
| chr5:180644729
|
G | A | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+4759C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644729 | ||||||
| chr5:180644812
|
G | A | 12 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(9): Show | 12 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+4676C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644812 | ||||||
| chr5:180644995
|
C | T | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.58+4493G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180644995 | ||||||
| chr5:180645088
|
C | T | 2 | a0001c0001t0001g0168a0002c0002t0003g0207 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58+4400G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645088 | ||||||
| chr5:180645239
|
C | T | 2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+4249G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645239 | ||||||
| chr5:180645249
|
G | A | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+4239C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645249 | ||||||
| chr5:180645275
|
C | T | 11 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(8): Show | 11 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+4213G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645275 | ||||||
| chr5:180645285
|
G | C | 11 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(8): Show | 11 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+4203C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645285 | ||||||
| chr5:180645322
|
C | T | 62 | a0001c0001t0001g0062a0001c0001t0001g0330a0001c0001t0001g0356others(59): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.58+4166G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645322 | ||||||
| chr5:180645332
|
G | A | 3 | a0001c0047t0001g0173a0005c0015t0011g0171a0005c0015t0011g0172 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.58+4156C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645332 | ||||||
| chr5:180645577
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.58+3911G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645577 | ||||||
| chr5:180645653
|
A | G | 231 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.58+3835T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645653 | ||||||
| chr5:180645698
|
G | A | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+3790C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645698 | ||||||
| chr5:180645703
|
C | T | 2 | a0003c0005t0001g0036a0003c0005t0001g0037 | 2 | HG01069.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.58+3785G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645703 | ||||||
| chr5:180645711
|
T | C | 13 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+3777A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645711 | ||||||
| chr5:180645851
|
T | A | 10 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(7): Show | 10 | HG01167.hp1 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+3637A>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180645851 | ||||||
| chr5:180646247
|
T | C | 22 | a0001c0001t0001g0062a0001c0001t0002g0066a0001c0001t0002g0067others(19): Show | 22 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+3241A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646247 | ||||||
| chr5:180646373
|
A | G | 219 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.58+3115T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646373 | ||||||
| chr5:180646385
|
G | A | 9 | a0001c0001t0001g0356a0001c0001t0012g0357a0001c0001t0012g0358others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3103C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646385 | ||||||
| chr5:180646424
|
C | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(93): Show | 96 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.58+3064G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646424 | ||||||
| chr5:180646485
|
T | C | 2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+3003A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646485 | ||||||
| chr5:180646609
|
G | C | 2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+2879C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646609 | ||||||
| chr5:180646609
|
G | T | 11 | a0001c0001t0001g0057a0001c0009t0001g0063a0002c0002t0001g0030others(8): Show | 11 | HG00280.hp1 HG01070.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+2879C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646609 | ||||||
| chr5:180646675
|
C | A | 1 | a0001c0001t0001g0360 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+2813G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646675 | ||||||
| chr5:180646724
|
C | T | 3 | a0001c0001t0001g0012a0001c0009t0004g0013a0002c0038t0004g0068 | 3 | NA18994.hp2 NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.58+2764G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646724 | ||||||
| chr5:180646857
|
C | T | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0002c0008t0004g0065 | 3 | NA18971.hp1 NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.58+2631G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646857 | ||||||
| chr5:180646876
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG02135.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.58+2612C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646876 | ||||||
| chr5:180646936
|
T | C | 184 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.58+2552A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180646936 | ||||||
| chr5:180647019
|
C | A | 1 | a0002c0003t0005g0318 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+2469G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647019 | ||||||
| chr5:180647024
|
C | T | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+2464G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647024 | ||||||
| chr5:180647144
|
A | T | 2 | a0002c0003t0010g0178a0029c0028t0010g0179 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+2344T>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647144 | ||||||
| chr5:180647248
|
T | C | 198 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.58+2240A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647248 | ||||||
| chr5:180647335
|
AGCTTGTG others(10): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.58+2136_58+2152del others(17): Show |
FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647335 | ||||||
| chr5:180647453
|
G | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+2035C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647453 | ||||||
| chr5:180647500
|
T | C | 1 | a0001c0001t0001g0320 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.58+1988A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647500 | ||||||
| chr5:180647566
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+1922G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647566 | ||||||
| chr5:180647627
|
T | C | 214 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.58+1861A>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647627 | ||||||
| chr5:180647662
|
C | T | 1 | a0001c0001t0002g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.58+1826G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647662 | ||||||
| chr5:180647785
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.58+1703C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647785 | ||||||
| chr5:180647789
|
G | C | 200 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.58+1699C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647789 | ||||||
| chr5:180647810
|
C | T | 1 | a0005c0018t0013g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58+1678G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647810 | ||||||
| chr5:180647990
|
C | T | 41 | a0001c0001t0001g0330a0001c0001t0001g0356a0001c0001t0001g0360others(38): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.58+1498G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180647990 | ||||||
| chr5:180648010
|
G | T | 1 | a0002c0002t0001g0061 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.58+1478C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648010 | ||||||
| chr5:180648470
|
G | A | 1 | a0002c0011t0004g0007 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.58+1018C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648470 | ||||||
| chr5:180648730
|
A | AT | 208 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.58+757dupA | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648730 | ||||||
| chr5:180648779
|
C | T | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+709G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648779 | ||||||
| chr5:180648832
|
G | A | 1 | a0007c0010t0010g0323 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58+656C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648832 | ||||||
| chr5:180648868
|
C | G | 1 | a0002c0002t0013g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.58+620G>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648868 | ||||||
| chr5:180648885
|
C | T | 1 | a0002c0003t0001g0164 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.58+603G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648885 | ||||||
| chr5:180648935
|
G | A | 1 | a0002c0008t0004g0324 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+553C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180648935 | ||||||
| chr5:180649118
|
G | A | 2 | a0013c0019t0008g0059a0013c0019t0008g0060 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58+370C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649118 | ||||||
| chr5:180649129
|
G | A | 160 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(157): Show | 161 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.58+359C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649129 | ||||||
| chr5:180649130
|
C | A | 160 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(157): Show | 161 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.58+358G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649130 | ||||||
| chr5:180649240
|
A | G | 155 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.58+248T>C | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649240 | ||||||
| chr5:180649276
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | NA18993.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.58+212C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649276 | ||||||
| chr5:180649328
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG02135.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.58+160C>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649328 | ||||||
| chr5:180649330
|
G | T | 1 | a0002c0004t0005g0026 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.58+158C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649330 | ||||||
| chr5:180649398
|
C | A | 1 | a0027c0042t0028g0379 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+90G>T | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649398 | ||||||
| chr5:180649403
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0022others(14): Show | 18 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.58+85G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649403 | ||||||
| chr5:180649419
|
C | T | 3 | a0001c0001t0010g0368a0002c0003t0001g0370a0002c0003t0007g0369 | 3 | HG02647.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.58+69G>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649419 | ||||||
| chr5:180649426
|
G | T | 2 | a0008c0025t0017g0009a0008c0027t0017g0008 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58+62C>A | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649426 | ||||||
| chr5:180649460
|
G | C | 12 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0010g0368others(9): Show | 12 | HG01167.hp1 HG02647.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+28C>G | FLT4 | ENSG00000037280.16 | transcript | ENST00000261937.11 | protein_coding | 1/29 | chr5 | 180649460 |