| geneid | 2317 |
|---|---|
| ensemblid | ENSG00000136068.16 |
| hgncid | 3755 |
| symbol | FLNB |
| name | filamin B |
| refseq_nuc | NM_001457.4 |
| refseq_prot | NP_001448.2 |
| ensembl_nuc | ENST00000295956.9 |
| ensembl_prot | ENSP00000295956.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 58008422 |
| end | 58172251 |
| strand | + |
| ver | v1.2 |
| region | chr3:58008422-58172251 |
| region5000 | chr3:58003422-58177251 |
| regionname0 | FLNB_chr3_58008422_58172251 |
| regionname5000 | FLNB_chr3_58003422_58177251 |
| 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 | 2602 | 70 | 26 | 15 | 16 | 3 | 10 | 12 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002 | 1/1 | 2602 | 54 | 13 | 20 | 1 | 7 | 11 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003 | 0/0 | 2602 | 12 | 5 | 0 | 6 | 0 | 1 | 5 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004 | 0/0 | 2602 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005 | 0/0 | 2602 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0006 | 0/0 | 2602 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0007 | 0/0 | 2602 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0008 | 0/0 | 2602 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0009 | 0/0 | 2602 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0010 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0011 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0012 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0013 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0014 | 0/0 | 2602 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0015 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0016 | 0/0 | 2602 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0017 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0018 | 0/0 | 2602 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0019 | 0/0 | 2602 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0020 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0021 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0022 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0023 | 0/0 | 2602 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0024 | 0/0 | 2602 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0025 | 0/0 | 2602 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0026 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0027 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| 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 | 7809 | 62 | 20 | 15 | 16 | 2 | 9 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0002 | 1/0 | 7809 | 22 | 5 | 7 | 0 | 4 | 5 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0003 | 0/0 | 7809 | 8 | 0 | 4 | 0 | 2 | 2 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0004 | 0/1 | 7809 | 7 | 1 | 3 | 0 | 0 | 2 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0005 | 0/0 | 7809 | 7 | 0 | 0 | 6 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0006 | 0/0 | 7809 | 5 | 3 | 2 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0007 | 0/0 | 7809 | 4 | 0 | 2 | 0 | 1 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0008 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0009 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0010 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0011 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0012 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0013 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0014 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0015 | 0/0 | 7809 | 2 | 0 | 2 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0016 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0017 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0018 | 0/0 | 7809 | 2 | 1 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0019 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0020 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0021 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0022 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0023 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0024 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0025 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0026 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0027 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0028 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0029 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0030 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0031 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0032 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0033 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0034 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0035 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0036 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0037 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0038 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0039 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0040 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0041 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0042 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0043 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0044 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0045 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0046 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0047 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0048 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0049 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0050 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0051 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0052 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0053 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0054 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0055 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0056 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| c0057 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| 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 | 1633 | 88 | 28 | 20 | 24 | 3 | 13 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0002 | 1/1 | 1633 | 61 | 22 | 19 | 0 | 7 | 11 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0003 | 0/0 | 1633 | 11 | 10 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0004 | 0/0 | 1633 | 8 | 8 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0005 | 0/0 | 1633 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0006 | 0/0 | 1633 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0007 | 0/0 | 1633 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0008 | 0/0 | 1633 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0009 | 0/0 | 1633 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0010 | 0/0 | 1633 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0011 | 0/0 | 1633 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0012 | 0/0 | 1633 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0013 | 0/0 | 1633 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| t0014 | 0/0 | 1633 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| 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 | 7809 | 62 | 20 | 15 | 16 | 2 | 9 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0014 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0019 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0026 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0027 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0030 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0031 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0053 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0002 | 1/0 | 7809 | 22 | 5 | 7 | 0 | 4 | 5 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0003 | 0/0 | 7809 | 8 | 0 | 4 | 0 | 2 | 2 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0004 | 0/1 | 7809 | 7 | 1 | 3 | 0 | 0 | 2 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0007 | 0/0 | 7809 | 4 | 0 | 2 | 0 | 1 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0008 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0012 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0015 | 0/0 | 7809 | 2 | 0 | 2 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0018 | 0/0 | 7809 | 2 | 1 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0020 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0036 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0044 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0051 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0005 | 0/0 | 7809 | 7 | 0 | 0 | 6 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0009 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0035 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0054 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0006 | 0/0 | 7809 | 5 | 3 | 2 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0021 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0041 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0042 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0043 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0010 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0011 | 0/0 | 7809 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0037 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0048 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0006c0017 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0006c0049 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0007c0016 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0008c0013 | 0/0 | 7809 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0009c0028 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0009c0034 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0010c0057 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0011c0056 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0012c0055 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0013c0022 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0014c0023 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0015c0024 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0016c0025 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0017c0046 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0018c0050 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0019c0045 | 0/0 | 7809 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0020c0052 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0021c0047 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0022c0040 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0023c0033 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0024c0032 | 0/0 | 7809 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0025c0029 | 0/0 | 7809 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0026c0038 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0027c0039 | 0/0 | 7809 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9441 | 56 | 14 | 15 | 16 | 2 | 9 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0001t0002 | 0/0 | 9441 | 4 | 4 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0001t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0001t0004 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0014t0001 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0019t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0026t0001 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0027t0001 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0030t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0031t0005 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0001c0053t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0002t0001 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0002t0002 | 1/0 | 9441 | 21 | 5 | 6 | 0 | 4 | 5 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0003t0001 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0003t0002 | 0/0 | 9441 | 6 | 0 | 3 | 0 | 2 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0003t0007 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0004t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0004t0002 | 0/1 | 9441 | 6 | 0 | 3 | 0 | 0 | 2 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0007t0002 | 0/0 | 9441 | 4 | 0 | 2 | 0 | 1 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0008t0002 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0008t0014 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0012t0002 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0015t0001 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0015t0003 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0018t0002 | 0/0 | 9441 | 2 | 1 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0020t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0036t0009 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0044t0001 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0002c0051t0008 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0005t0001 | 0/0 | 9441 | 7 | 0 | 0 | 6 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0009t0004 | 0/0 | 9441 | 3 | 3 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0035t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0003c0054t0013 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0006t0002 | 0/0 | 9441 | 4 | 2 | 2 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0006t0012 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0021t0001 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0041t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0042t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0004c0043t0002 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0010t0002 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0010t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0011t0003 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0011t0004 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0037t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0005c0048t0005 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0006c0017t0006 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0006c0049t0002 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0007c0016t0004 | 0/0 | 9441 | 2 | 2 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0008c0013t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0008c0013t0011 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0009c0028t0002 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0009c0034t0002 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0010c0057t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0011c0056t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0012c0055t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0013c0022t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0014c0023t0001 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0015c0024t0002 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0016c0025t0010 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0017c0046t0003 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0018c0050t0002 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0019c0045t0002 | 0/0 | 9441 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0020c0052t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0021c0047t0004 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0022c0040t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0023c0033t0001 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0024c0032t0001 | 0/0 | 9441 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0025c0029t0001 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0026c0038t0002 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| a0027c0039t0001 | 0/0 | 9441 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | copy fasta | chr3 | 58003422 | 58177251 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0014t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0014t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0019t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0026t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0027t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0030t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0031t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0001c0053t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0003t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0007t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0007t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0007t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0007t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0008t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0008t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0008t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0012t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0012t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0015t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0015t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0018t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0018t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0020t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0036t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0044t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0002c0051t0008g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0009t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0009t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0009t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0035t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0003c0054t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0006t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0006t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0006t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0021t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0041t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0042t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0004c0043t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0010t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0010t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0010t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0011t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0011t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0011t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0037t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0005c0048t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0006c0017t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0006c0017t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0006c0049t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0007c0016t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0007c0016t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0008c0013t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0008c0013t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0009c0028t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0009c0034t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0010c0057t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0011c0056t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0012c0055t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0013c0022t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0014c0023t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0015c0024t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0016c0025t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0017c0046t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0018c0050t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0019c0045t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0020c0052t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0021c0047t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0022c0040t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0023c0033t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0024c0032t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0025c0029t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0026c0038t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| a0027c0039t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0002 | g0133 | EUR | GBR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0150 | EUR | FIN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00280 | hp2 | a0002 | c0007 | t0002 | g0177 | EUR | FIN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00438 | hp2 | a0003 | c0005 | t0001 | g0077 | EAS | CHS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00738 | hp2 | a0002 | c0003 | t0002 | g0140 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0171 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01071 | hp2 | a0002 | c0044 | t0001 | g0167 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0134 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01106 | hp1 | a0002 | c0018 | t0002 | g0173 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0141 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01109 | hp1 | a0002 | c0015 | t0003 | g0025 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01167 | hp1 | a0002 | c0015 | t0001 | g0131 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01167 | hp2 | a0004 | c0006 | t0002 | g0068 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01169 | hp1 | a0004 | c0006 | t0002 | g0102 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0163 | AMR | PUR | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01255 | hp1 | a0004 | c0021 | t0001 | g0121 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01257 | hp1 | a0002 | c0004 | t0002 | g0072 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01261 | hp1 | a0002 | c0007 | t0002 | g0175 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01358 | hp1 | a0002 | c0007 | t0002 | g0164 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0139 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01361 | hp2 | a0002 | c0004 | t0002 | g0069 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01516 | hp1 | a0002 | c0003 | t0002 | g0138 | EUR | IBS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01884 | hp1 | a0002 | c0012 | t0002 | g0152 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0148 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01891 | hp1 | a0011 | c0056 | t0001 | g0112 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01891 | hp2 | a0002 | c0020 | t0003 | g0123 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01975 | hp1 | a0002 | c0004 | t0002 | g0106 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02004 | hp2 | a0009 | c0034 | t0002 | g0104 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02040 | hp1 | a0002 | c0036 | t0009 | g0075 | EAS | KHV | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02055 | hp2 | a0012 | c0055 | t0001 | g0010 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02145 | hp2 | a0002 | c0018 | t0002 | g0136 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02280 | hp2 | a0003 | c0009 | t0004 | g0017 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0162 | AMR | PEL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02451 | hp2 | a0007 | c0016 | t0004 | g0095 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02572 | hp2 | a0006 | c0017 | t0006 | g0024 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02615 | hp1 | a0017 | c0046 | t0003 | g0015 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02615 | hp2 | a0004 | c0042 | t0003 | g0157 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02630 | hp1 | a0020 | c0052 | t0001 | g0117 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02647 | hp1 | a0027 | c0039 | t0001 | g0067 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02647 | hp2 | a0005 | c0011 | t0003 | g0011 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02735 | hp1 | a0003 | c0005 | t0001 | g0172 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02735 | hp2 | a0024 | c0032 | t0001 | g0154 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02818 | hp2 | a0004 | c0006 | t0002 | g0048 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02896 | hp2 | a0008 | c0013 | t0011 | g0180 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02897 | hp1 | a0008 | c0013 | t0001 | g0066 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02897 | hp2 | a0003 | c0009 | t0004 | g0026 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02922 | hp1 | a0002 | c0008 | t0014 | g0110 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02965 | hp2 | a0026 | c0038 | t0002 | g0158 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02970 | hp1 | a0001 | c0030 | t0003 | g0128 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02970 | hp2 | a0004 | c0043 | t0002 | g0049 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03041 | hp1 | a0004 | c0041 | t0001 | g0016 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03041 | hp2 | a0003 | c0009 | t0004 | g0009 | AFR | GWD | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03139 | hp1 | a0006 | c0049 | t0002 | g0023 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03139 | hp2 | a0005 | c0011 | t0004 | g0142 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03195 | hp2 | a0002 | c0008 | t0002 | g0022 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03209 | hp1 | a0002 | c0012 | t0002 | g0118 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03225 | hp2 | a0006 | c0017 | t0006 | g0057 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03239 | hp1 | a0009 | c0028 | t0002 | g0071 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03239 | hp2 | a0001 | c0027 | t0001 | g0113 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03453 | hp1 | a0005 | c0010 | t0003 | g0002 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03453 | hp2 | a0015 | c0024 | t0002 | g0012 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03486 | hp1 | a0003 | c0054 | t0013 | g0108 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03486 | hp2 | a0001 | c0019 | t0001 | g0122 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0073 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0052 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03516 | hp1 | a0021 | c0047 | t0004 | g0093 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03579 | hp1 | a0010 | c0057 | t0001 | g0046 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03579 | hp2 | a0001 | c0014 | t0001 | g0115 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03704 | hp2 | a0002 | c0007 | t0002 | g0174 | SAS | PJL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03834 | hp1 | a0023 | c0033 | t0001 | g0039 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03834 | hp2 | a0018 | c0050 | t0002 | g0082 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03927 | hp1 | a0002 | c0003 | t0007 | g0127 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG04184 | hp1 | a0002 | c0004 | t0002 | g0074 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG04184 | hp2 | a0002 | c0051 | t0008 | g0153 | SAS | BEB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | STU | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18522 | hp2 | a0007 | c0016 | t0004 | g0096 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18906 | hp2 | a0005 | c0011 | t0003 | g0119 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18942 | hp1 | a0025 | c0029 | t0001 | g0008 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18978 | hp1 | a0014 | c0023 | t0001 | g0081 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18979 | hp1 | a0003 | c0005 | t0001 | g0080 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18988 | hp1 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19004 | hp1 | a0003 | c0005 | t0001 | g0100 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19009 | hp1 | a0016 | c0025 | t0010 | g0031 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19012 | hp2 | a0003 | c0005 | t0001 | g0044 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19030 | hp1 | a0013 | c0022 | t0001 | g0116 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19043 | hp2 | a0005 | c0037 | t0003 | g0129 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19084 | hp1 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19240 | hp1 | a0001 | c0053 | t0001 | g0018 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA19240 | hp2 | a0004 | c0006 | t0002 | g0050 | AFR | YRI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20129 | hp2 | a0022 | c0040 | t0001 | g0019 | AFR | ASW | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0166 | EUR | TSI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0135 | EUR | TSI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20805 | hp2 | a0001 | c0026 | t0001 | g0149 | EUR | TSI | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | GIH | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20905 | hp2 | a0002 | c0004 | t0002 | g0170 | SAS | GIH | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01123 | hp1 | a0019 | c0045 | t0002 | g0159 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0156 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02109 | hp2 | a0001 | c0014 | t0001 | g0111 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02559 | hp1 | a0005 | c0048 | t0005 | g0001 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG02559 | hp2 | a0005 | c0010 | t0002 | g0013 | AFR | ACB | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03471 | hp1 | a0002 | c0008 | t0002 | g0155 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG03471 | hp2 | a0003 | c0035 | t0003 | g0060 | AFR | MSL | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG06807 | hp1 | a0005 | c0010 | t0002 | g0065 | AFR | USA | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| HG06807 | hp2 | a0004 | c0006 | t0012 | g0109 | AFR | USA | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | USA | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA21309 | hp1 | a0001 | c0031 | t0005 | g0145 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0002 | g0130 | REF | REF | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0161 | REF | REF | FLNB_chr3_58003422_58177251 | FLNB | chr3 | 58003422 | 58177251 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58077115
|
A | T | 2 | a0010a0011 | 2 | HG01891.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.362A>T | p.Tyr121Phe | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/46 | 505/9441 | 362/7809 | 121/2602 | chr3 | 58077115 | ||
| chr3:58081657
|
C | T | 1 | a0012 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.668C>T | p.Pro223Leu | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/46 | 811/9441 | 668/7809 | 223/2602 | chr3 | 58081657 | ||
| chr3:58106851
|
C | T | 1 | a0006 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1919C>T | p.Thr640Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/46 | 2062/9441 | 1919/7809 | 640/2602 | chr3 | 58106851 | ||
| chr3:58110043
|
G | A | 1 | a0013 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2357G>A | p.Arg786Gln | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/46 | 2500/9441 | 2357/7809 | 786/2602 | chr3 | 58110043 | ||
| chr3:58110147
|
A | G | 1 | a0027 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2461A>G | p.Ile821Val | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/46 | 2604/9441 | 2461/7809 | 821/2602 | chr3 | 58110147 | ||
| chr3:58111800
|
G | A | 1 | a0011 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2494G>A | p.Ala832Thr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 17/46 | 2637/9441 | 2494/7809 | 832/2602 | chr3 | 58111800 | ||
| chr3:58121429
|
G | A | 1 | a0014 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.3052G>A | p.Val1018Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/46 | 3195/9441 | 3052/7809 | 1018/2602 | chr3 | 58121429 | ||
| chr3:58123129
|
G | A | 2 | a0011a0015 | 2 | HG01891.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.3163G>A | p.Val1055Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3306/9441 | 3163/7809 | 1055/2602 | chr3 | 58123129 | ||
| chr3:58123135
|
A | C | 2 | a0013a0026 | 2 | HG02965.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.3169A>C | p.Lys1057Gln | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3312/9441 | 3169/7809 | 1057/2602 | chr3 | 58123135 | ||
| chr3:58123375
|
G | A | 1 | a0016 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.3409G>A | p.Val1137Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3552/9441 | 3409/7809 | 1137/2602 | chr3 | 58123375 | ||
| chr3:58123435
|
G | A | 9 | a0001a0008a0009others(6): Show | 80 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
missense_variant | MODERATE | c.3469G>A | p.Asp1157Asn | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3612/9441 | 3469/7809 | 1157/2602 | chr3 | 58123435 | ||
| chr3:58123501
|
G | A | 3 | a0004a0010a0022 | 11 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(8): Show |
missense_variant | MODERATE | c.3535G>A | p.Glu1179Lys | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3678/9441 | 3535/7809 | 1179/2602 | chr3 | 58123501 | ||
| chr3:58124464
|
C | T | 3 | a0005a0007a0021 | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
missense_variant | MODERATE | c.3857C>T | p.Ala1286Val | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/46 | 4000/9441 | 3857/7809 | 1286/2602 | chr3 | 58124464 | ||
| chr3:58125722
|
A | G | 1 | a0020 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.4040A>G | p.Asn1347Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/46 | 4183/9441 | 4040/7809 | 1347/2602 | chr3 | 58125722 | ||
| chr3:58132828
|
G | A | 12 | a0001a0003a0004others(9): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
missense_variant | MODERATE | c.4411G>A | p.Val1471Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/46 | 4554/9441 | 4411/7809 | 1471/2602 | chr3 | 58132828 | ||
| chr3:58136139
|
C | T | 1 | a0015 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4832C>T | p.Thr1611Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/46 | 4975/9441 | 4832/7809 | 1611/2602 | chr3 | 58136139 | ||
| chr3:58138353
|
A | G | 1 | a0023 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.4933A>G | p.Lys1645Glu | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/46 | 5076/9441 | 4933/7809 | 1645/2602 | chr3 | 58138353 | ||
| chr3:58138354
|
A | C | 1 | a0023 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.4934A>C | p.Lys1645Thr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/46 | 5077/9441 | 4934/7809 | 1645/2602 | chr3 | 58138354 | ||
| chr3:58148293
|
C | T | 1 | a0024 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.5816C>T | p.Thr1939Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/46 | 5959/9441 | 5816/7809 | 1939/2602 | chr3 | 58148293 | ||
| chr3:58148778
|
A | G | 1 | a0019 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.6017A>G | p.Lys2006Arg | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/46 | 6160/9441 | 6017/7809 | 2006/2602 | chr3 | 58148778 | ||
| chr3:58149951
|
G | A | 1 | a0017 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.6193G>A | p.Val2065Met | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 37/46 | 6336/9441 | 6193/7809 | 2065/2602 | chr3 | 58149951 | ||
| chr3:58149984
|
G | A | 1 | a0025 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.6226G>A | p.Ala2076Thr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 37/46 | 6369/9441 | 6226/7809 | 2076/2602 | chr3 | 58149984 | ||
| chr3:58154839
|
T | C | 1 | a0022 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.6683T>C | p.Ile2228Thr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/46 | 6826/9441 | 6683/7809 | 2228/2602 | chr3 | 58154839 | ||
| chr3:58163231
|
G | A | 2 | a0007a0021 | 3 | HG02451.hp2 HG03516.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.7099G>A | p.Val2367Ile | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/46 | 7242/9441 | 7099/7809 | 2367/2602 | chr3 | 58163231 | ||
| chr3:58163298
|
C | T | 1 | a0021 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.7166C>T | p.Ala2389Val | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/46 | 7309/9441 | 7166/7809 | 2389/2602 | chr3 | 58163298 | ||
| chr3:58168466
|
A | G | 1 | a0018 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.7225A>G | p.Thr2409Ala | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/46 | 7368/9441 | 7225/7809 | 2409/2602 | chr3 | 58168466 | ||
| chr3:58169620
|
A | G | 1 | a0008 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.7448A>G | p.Asn2483Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/46 | 7591/9441 | 7448/7809 | 2483/2602 | chr3 | 58169620 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58008813
|
G | A | 3 | a0001c0019a0002c0020a0004c0021 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.249G>A | p.Ala83Ala | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/46 | 392/9441 | 249/7809 | 83/2602 | chr3 | 58008813 | ||
| chr3:58081658
|
G | A | 1 | a0002c0012 | 2 | HG01884.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.669G>A | p.Pro223Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/46 | 812/9441 | 669/7809 | 223/2602 | chr3 | 58081658 | ||
| chr3:58081709
|
C | T | 1 | a0003c0054 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.720C>T | p.Ala240Ala | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/46 | 863/9441 | 720/7809 | 240/2602 | chr3 | 58081709 | ||
| chr3:58094840
|
C | T | 1 | a0001c0053 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.792C>T | p.Ile264Ile | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/46 | 935/9441 | 792/7809 | 264/2602 | chr3 | 58094840 | ||
| chr3:58096161
|
T | C | 28 | a0001c0001a0001c0019a0001c0026others(25): Show | 107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
synonymous_variant | LOW | c.927T>C | p.Ser309Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/46 | 1070/9441 | 927/7809 | 309/2602 | chr3 | 58096161 | ||
| chr3:58106801
|
C | T | 4 | a0002c0018a0002c0051a0018c0050others(1): Show | 5 | HG01106.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.1869C>T | p.Asp623Asp | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/46 | 2012/9441 | 1869/7809 | 623/2602 | chr3 | 58106801 | ||
| chr3:58110068
|
C | T | 2 | a0004c0021a0010c0057 | 2 | HG01255.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.2382C>T | p.Asp794Asp | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/46 | 2525/9441 | 2382/7809 | 794/2602 | chr3 | 58110068 | ||
| chr3:58121284
|
G | A | 2 | a0006c0017a0006c0049 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.2907G>A | p.Arg969Arg | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/46 | 3050/9441 | 2907/7809 | 969/2602 | chr3 | 58121284 | ||
| chr3:58121467
|
C | T | 1 | a0002c0008 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.3090C>T | p.Tyr1030Tyr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/46 | 3233/9441 | 3090/7809 | 1030/2602 | chr3 | 58121467 | ||
| chr3:58123206
|
G | A | 2 | a0004c0041a0022c0040 | 2 | HG03041.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.3240G>A | p.Pro1080Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/46 | 3383/9441 | 3240/7809 | 1080/2602 | chr3 | 58123206 | ||
| chr3:58124378
|
G | A | 1 | a0001c0026 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.3771G>A | p.Pro1257Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/46 | 3914/9441 | 3771/7809 | 1257/2602 | chr3 | 58124378 | ||
| chr3:58125732
|
C | A | 1 | a0001c0027 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.4050C>A | p.Thr1350Thr | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/46 | 4193/9441 | 4050/7809 | 1350/2602 | chr3 | 58125732 | ||
| chr3:58126713
|
A | G | 52 | a0001c0001a0001c0014a0001c0019others(49): Show | 148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
synonymous_variant | LOW | c.4173A>G | p.Ala1391Ala | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/46 | 4316/9441 | 4173/7809 | 1391/2602 | chr3 | 58126713 | ||
| chr3:58126761
|
C | T | 39 | a0001c0001a0001c0014a0001c0019others(36): Show | 120 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
splice_region_variant&synonymous_variant | LOW | c.4221C>T | p.Pro1407Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/46 | 4364/9441 | 4221/7809 | 1407/2602 | chr3 | 58126761 | ||
| chr3:58130880
|
G | A | 2 | a0011c0056a0015c0024 | 2 | HG01891.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.4362G>A | p.Pro1454Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/46 | 4505/9441 | 4362/7809 | 1454/2602 | chr3 | 58130880 | ||
| chr3:58130895
|
T | C | 2 | a0011c0056a0015c0024 | 2 | HG01891.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.4377T>C | p.Val1459Val | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/46 | 4520/9441 | 4377/7809 | 1459/2602 | chr3 | 58130895 | ||
| chr3:58146911
|
G | A | 2 | a0002c0008a0011c0056 | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.5646G>A | p.Pro1882Pro | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/46 | 5789/9441 | 5646/7809 | 1882/2602 | chr3 | 58146911 | ||
| chr3:58148246
|
C | T | 1 | a0002c0036 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.5769C>T | p.Ala1923Ala | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/46 | 5912/9441 | 5769/7809 | 1923/2602 | chr3 | 58148246 | ||
| chr3:58153445
|
G | A | 11 | a0001c0030a0003c0054a0004c0006others(8): Show | 17 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(14): Show |
synonymous_variant | LOW | c.6438G>A | p.Val2146Val | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/46 | 6581/9441 | 6438/7809 | 2146/2602 | chr3 | 58153445 | ||
| chr3:58168450
|
G | A | 4 | a0002c0007a0002c0018a0012c0055others(1): Show | 8 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
synonymous_variant | LOW | c.7209G>A | p.Ser2403Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/46 | 7352/9441 | 7209/7809 | 2403/2602 | chr3 | 58168450 | ||
| chr3:58168495
|
C | T | 1 | a0024c0032 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.7254C>T | p.Ser2418Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/46 | 7397/9441 | 7254/7809 | 2418/2602 | chr3 | 58168495 | ||
| chr3:58168600
|
C | T | 27 | a0001c0001a0001c0014a0001c0019others(24): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
synonymous_variant | LOW | c.7359C>T | p.Ser2453Ser | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/46 | 7502/9441 | 7359/7809 | 2453/2602 | chr3 | 58168600 | ||
| chr3:58170621
|
C | T | 1 | a0003c0054 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.7668C>T | p.Cys2556Cys | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 7811/9441 | 7668/7809 | 2556/2602 | chr3 | 58170621 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58008434
|
G | C | 1 | a0002c0003t0007 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/46 | 131 | chr3 | 58008434 | |||||
| chr3:58008534
|
C | T | 3 | a0002c0008t0014a0003c0054t0013a0004c0006t0012 | 3 | HG02922.hp1 HG03486.hp1 HG06807.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/46 | chr3 | 58008534 | ||||||
| chr3:58008556
|
G | T | 1 | a0008c0013t0011 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/46 | 9 | chr3 | 58008556 | |||||
| chr3:58170962
|
C | T | 7 | a0001c0001t0004a0002c0008t0014a0003c0009t0004others(4): Show | 11 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 200 | chr3 | 58170962 | |||||
| chr3:58171241
|
G | T | 7 | a0001c0001t0004a0002c0008t0014a0003c0009t0004others(4): Show | 11 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*479G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 479 | chr3 | 58171241 | |||||
| chr3:58171343
|
C | T | 2 | a0001c0031t0005a0005c0048t0005 | 2 | HG02559.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 581 | chr3 | 58171343 | |||||
| chr3:58171354
|
C | G | 6 | a0001c0001t0004a0002c0008t0014a0003c0009t0004others(3): Show | 9 | HG02280.hp2 HG02451.hp2 HG02897.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 592 | chr3 | 58171354 | |||||
| chr3:58171419
|
T | C | 7 | a0001c0001t0004a0002c0008t0014a0003c0009t0004others(4): Show | 11 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*657T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 657 | chr3 | 58171419 | |||||
| chr3:58171534
|
C | T | 1 | a0016c0025t0010 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*772C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 772 | chr3 | 58171534 | |||||
| chr3:58171792
|
G | C | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(48): Show | 118 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1030G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 1030 | chr3 | 58171792 | |||||
| chr3:58171884
|
T | C | 19 | a0001c0001t0003a0001c0001t0004a0001c0030t0003others(16): Show | 24 | HG01109.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1122T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 1122 | chr3 | 58171884 | |||||
| chr3:58171979
|
G | A | 7 | a0001c0001t0004a0002c0008t0014a0003c0009t0004others(4): Show | 11 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1217G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 1217 | chr3 | 58171979 | |||||
| chr3:58172132
|
G | A | 7 | a0001c0001t0004a0002c0008t0014a0002c0051t0008others(4): Show | 10 | HG02280.hp2 HG02451.hp2 HG02897.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1370G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 1370 | chr3 | 58172132 | |||||
| chr3:58172212
|
G | T | 1 | a0002c0036t0009 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1450G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 46/46 | 1450 | chr3 | 58172212 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:58008864
|
C | A | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
splice_region_variant&intron_variant | LOW | c.292+8C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58008864 | ||||||
| chr3:58008868
|
G | T | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+12G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58008868 | ||||||
| chr3:58008902
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292+46G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58008902 | ||||||
| chr3:58008924
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.292+68G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58008924 | ||||||
| chr3:58008992
|
T | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.292+136T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58008992 | ||||||
| chr3:58009139
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0002c0002t0002g0006 | 3 | HG01109.hp2 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.292+283G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009139 | ||||||
| chr3:58009294
|
G | A | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+438G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009294 | ||||||
| chr3:58009571
|
C | G | 1 | a0002c0002t0002g0006 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.292+715C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009571 | ||||||
| chr3:58009921
|
A | C | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+1065A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009921 | ||||||
| chr3:58009974
|
G | T | 3 | a0002c0004t0001g0156a0002c0008t0002g0155a0004c0042t0003g0157 | 3 | HG02109.hp1 HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+1118G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009974 | ||||||
| chr3:58009979
|
C | T | 32 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.292+1123C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58009979 | ||||||
| chr3:58010179
|
C | G | 35 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.292+1323C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010179 | ||||||
| chr3:58010633
|
A | G | 3 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292+1777A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010633 | ||||||
| chr3:58010923
|
C | T | 9 | a0002c0002t0002g0120a0002c0004t0001g0156a0002c0008t0002g0155others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+2067C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010923 | ||||||
| chr3:58010925
|
C | T | 1 | a0001c0014t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.292+2069C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010925 | ||||||
| chr3:58010928
|
C | T | 9 | a0002c0002t0002g0120a0002c0004t0001g0156a0002c0008t0002g0155others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+2072C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010928 | ||||||
| chr3:58010951
|
T | C | 9 | a0002c0002t0002g0120a0002c0004t0001g0156a0002c0008t0002g0155others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+2095T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010951 | ||||||
| chr3:58010957
|
C | A | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+2101C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010957 | ||||||
| chr3:58010999
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.292+2143C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58010999 | ||||||
| chr3:58011016
|
G | C | 1 | a0001c0001t0001g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.292+2160G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011016 | ||||||
| chr3:58011178
|
C | T | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292+2322C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011178 | ||||||
| chr3:58011179
|
G | T | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.292+2323G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011179 | ||||||
| chr3:58011202
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+2346G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011202 | ||||||
| chr3:58011203
|
C | T | 2 | a0020c0052t0001g0117a0026c0038t0002g0158 | 2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.292+2347C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011203 | ||||||
| chr3:58011270
|
T | A | 1 | a0025c0029t0001g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.292+2414T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011270 | ||||||
| chr3:58011337
|
C | T | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+2481C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011337 | ||||||
| chr3:58011520
|
C | A | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+2664C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011520 | ||||||
| chr3:58011728
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.292+2872T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011728 | ||||||
| chr3:58011823
|
TA | T | 2 | a0003c0005t0001g0043a0003c0005t0001g0044 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.292+2968delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011823 | ||||||
| chr3:58011875
|
C | T | 19 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0032others(16): Show | 19 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+3019C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011875 | ||||||
| chr3:58011878
|
C | A | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+3022C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011878 | ||||||
| chr3:58011899
|
G | A | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+3043G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58011899 | ||||||
| chr3:58012159
|
C | T | 4 | a0001c0014t0001g0111a0002c0008t0014g0110a0003c0054t0013g0108others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3303C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012159 | ||||||
| chr3:58012209
|
CA | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 41 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.292+3375delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58012209 | |||||
| chr3:58012209
|
CAA | C | 9 | a0001c0001t0001g0027a0001c0019t0001g0122a0002c0002t0002g0124others(6): Show | 9 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+3374_292+3375d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58012209 | |||||
| chr3:58012209
|
CAAA | C | 35 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.292+3373_292+3375d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58012209 | |||||
| chr3:58012209
|
CAAAA | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.292+3372_292+3375d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58012209 | |||||
| chr3:58012209
|
CAAAAA | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0105others(5): Show | 8 | HG01123.hp2 HG01169.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+3371_292+3375d others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58012209 | |||||
| chr3:58012257
|
G | A | 1 | a0003c0009t0004g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292+3401G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012257 | ||||||
| chr3:58012340
|
T | C | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+3484T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012340 | ||||||
| chr3:58012388
|
T | C | 5 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119others(2): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+3532T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012388 | ||||||
| chr3:58012389
|
G | T | 5 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119others(2): Show | 5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+3533G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012389 | ||||||
| chr3:58012570
|
C | A | 1 | a0010c0057t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+3714C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012570 | ||||||
| chr3:58012601
|
A | C | 1 | a0010c0057t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+3745A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012601 | ||||||
| chr3:58012641
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.292+3785C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012641 | ||||||
| chr3:58012726
|
T | G | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+3870T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012726 | ||||||
| chr3:58012730
|
G | T | 1 | a0008c0013t0011g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292+3874G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58012730 | ||||||
| chr3:58013030
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0051a0004c0006t0002g0048others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4174G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013030 | ||||||
| chr3:58013044
|
G | T | 4 | a0001c0001t0001g0168a0002c0002t0002g0165a0002c0002t0002g0166others(1): Show | 4 | HG01071.hp2 HG01255.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+4188G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013044 | ||||||
| chr3:58013163
|
G | A | 1 | a0002c0002t0002g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.292+4307G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013163 | ||||||
| chr3:58013212
|
T | C | 1 | a0002c0012t0002g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292+4356T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013212 | ||||||
| chr3:58013259
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(78): Show | 81 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+4403C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013259 | ||||||
| chr3:58013380
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.292+4524T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013380 | ||||||
| chr3:58013381
|
G | A | 4 | a0001c0014t0001g0111a0002c0008t0014g0110a0003c0054t0013g0108others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+4525G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013381 | ||||||
| chr3:58013461
|
A | C | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+4605A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013461 | ||||||
| chr3:58013508
|
G | A | 3 | a0002c0008t0014g0110a0003c0054t0013g0108a0004c0006t0012g0109 | 3 | HG02922.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.292+4652G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013508 | ||||||
| chr3:58013593
|
G | C | 1 | a0003c0009t0004g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292+4737G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013593 | ||||||
| chr3:58013677
|
A | G | 2 | a0003c0009t0004g0009a0015c0024t0002g0012 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292+4821A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013677 | ||||||
| chr3:58013715
|
G | A | 2 | a0001c0001t0001g0014a0005c0010t0002g0013 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.292+4859G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013715 | ||||||
| chr3:58013751
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0051a0004c0006t0002g0048others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4895G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58013751 | ||||||
| chr3:58014048
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01169.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+5192T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014048 | ||||||
| chr3:58014091
|
TTTATGGT others(15): Show |
T | 3 | a0002c0004t0001g0156a0002c0008t0002g0155a0004c0042t0003g0157 | 3 | HG02109.hp1 HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+5237_292+5258d others(24): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58014091 | |||||
| chr3:58014209
|
G | A | 7 | a0002c0002t0002g0120a0002c0004t0001g0156a0002c0008t0002g0155others(4): Show | 7 | HG02109.hp1 HG02615.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+5353G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014209 | ||||||
| chr3:58014263
|
G | T | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+5407G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014263 | ||||||
| chr3:58014310
|
C | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(33): Show | 36 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.292+5454C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014310 | ||||||
| chr3:58014382
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18979.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.292+5526C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014382 | ||||||
| chr3:58014511
|
G | A | 3 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292+5655G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014511 | ||||||
| chr3:58014715
|
A | G | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.292+5859A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014715 | ||||||
| chr3:58014821
|
C | T | 1 | a0003c0005t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.292+5965C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014821 | ||||||
| chr3:58014878
|
G | A | 1 | a0001c0014t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.292+6022G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014878 | ||||||
| chr3:58014937
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+6081C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58014937 | ||||||
| chr3:58015261
|
G | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.292+6405G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015261 | ||||||
| chr3:58015432
|
C | T | 1 | a0002c0007t0002g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.292+6576C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015432 | ||||||
| chr3:58015647
|
G | T | 2 | a0003c0009t0004g0009a0015c0024t0002g0012 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292+6791G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015647 | ||||||
| chr3:58015704
|
G | A | 8 | a0002c0002t0002g0120a0002c0004t0001g0156a0002c0008t0002g0155others(5): Show | 8 | HG02109.hp1 HG02615.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+6848G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015704 | ||||||
| chr3:58015846
|
T | A | 3 | a0001c0001t0001g0003a0006c0017t0006g0057a0010c0057t0001g0046 | 3 | HG02630.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.292+6990T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015846 | ||||||
| chr3:58015884
|
G | A | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.292+7028G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58015884 | ||||||
| chr3:58016142
|
C | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0002g0058others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+7286C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016142 | ||||||
| chr3:58016152
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.292+7296C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016152 | ||||||
| chr3:58016178
|
GC | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.292+7324delC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58016178 | |||||
| chr3:58016245
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292+7389G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016245 | ||||||
| chr3:58016379
|
C | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(78): Show | 81 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+7523C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016379 | ||||||
| chr3:58016435
|
A | G | 1 | a0002c0012t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+7579A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016435 | ||||||
| chr3:58016457
|
GC | G | 31 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.292+7605delC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58016457 | |||||
| chr3:58016467
|
C | CAT | 12 | a0001c0014t0001g0111a0002c0002t0002g0120a0002c0004t0001g0156others(9): Show | 12 | HG02109.hp1 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+7624_292+7625d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58016467 | |||||
| chr3:58016700
|
T | C | 3 | a0002c0008t0014g0110a0003c0054t0013g0108a0004c0006t0012g0109 | 3 | HG02922.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.292+7844T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016700 | ||||||
| chr3:58016710
|
A | G | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+7854A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016710 | ||||||
| chr3:58016785
|
C | A | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+7929C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016785 | ||||||
| chr3:58016904
|
A | G | 2 | a0020c0052t0001g0117a0026c0038t0002g0158 | 2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.292+8048A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58016904 | ||||||
| chr3:58017060
|
T | C | 3 | a0002c0004t0001g0156a0002c0008t0002g0155a0004c0042t0003g0157 | 3 | HG02109.hp1 HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+8204T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017060 | ||||||
| chr3:58017158
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.292+8302C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017158 | ||||||
| chr3:58017161
|
G | A | 1 | a0002c0002t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292+8305G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017161 | ||||||
| chr3:58017315
|
A | G | 5 | a0001c0014t0001g0111a0002c0008t0014g0110a0003c0054t0013g0108others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+8459A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017315 | ||||||
| chr3:58017400
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.292+8544G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017400 | ||||||
| chr3:58017407
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+8551C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017407 | ||||||
| chr3:58017413
|
G | A | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+8557G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017413 | ||||||
| chr3:58017545
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292+8689G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58017545 | ||||||
| chr3:58018327
|
C | CT | 14 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0014t0001g0111others(11): Show | 14 | HG00280.hp2 HG00741.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.292+9497dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58018327 | |||||
| chr3:58018327
|
C | CTT | 9 | a0001c0001t0001g0051a0001c0001t0001g0092a0001c0001t0001g0094others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+9496_292+9497d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58018327 | |||||
| chr3:58018327
|
CT | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(75): Show | 78 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.292+9497delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58018327 | |||||
| chr3:58018579
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+9723G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58018579 | ||||||
| chr3:58018761
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292+9905G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58018761 | ||||||
| chr3:58018815
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.292+9959G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58018815 | ||||||
| chr3:58018954
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.292+10098C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58018954 | ||||||
| chr3:58018962
|
C | CA | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0027others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+10129dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58018962 | |||||
| chr3:58018962
|
CA | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0107others(5): Show | 8 | HG01975.hp1 HG01975.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+10129delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58018962 | |||||
| chr3:58018969
|
A | C | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+10113A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58018969 | ||||||
| chr3:58019395
|
C | T | 4 | a0001c0014t0001g0111a0002c0008t0014g0110a0003c0054t0013g0108others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+10539C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58019395 | ||||||
| chr3:58019676
|
AT | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+10828delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58019676 | |||||
| chr3:58019709
|
C | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+10853C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58019709 | ||||||
| chr3:58020043
|
A | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.292+11187A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020043 | ||||||
| chr3:58020048
|
G | GGT | 31 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0028others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.292+11239_292+1124 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
G | GGTGT | 14 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0101others(11): Show | 14 | HG00741.hp2 HG01255.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.292+11237_292+1124 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
G | GGTGTGT | 17 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0097others(14): Show | 17 | HG00738.hp1 HG01123.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.292+11235_292+1124 others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0003g0089others(3): Show | 6 | HG01192.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+11233_292+1124 others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
G | GGTGTGTG others(3): Show |
1 | a0002c0002t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.292+11231_292+1124 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
G | T | 1 | a0002c0002t0001g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292+11192G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020048 | ||||||
| chr3:58020048
|
GGT | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0020others(22): Show | 25 | HG01106.hp1 HG01192.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.292+11239_292+1124 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGT | G | 40 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.292+11237_292+1124 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGTGT | G | 7 | a0001c0001t0001g0151a0001c0014t0001g0111a0001c0026t0001g0149others(4): Show | 7 | HG02109.hp2 HG02647.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+11235_292+1124 others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGTGTG others(1): Show |
G | 9 | a0001c0001t0001g0051a0002c0004t0001g0156a0002c0008t0002g0155others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+11233_292+1124 others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGTGTG others(3): Show |
G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+11231_292+1124 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGTGTG others(5): Show |
G | 3 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292+11229_292+1124 others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020048
|
GGTGTGTG others(13): Show |
G | 1 | a0010c0057t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+11221_292+1124 others(24): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020048 | |||||
| chr3:58020095
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+11239G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020095 | ||||||
| chr3:58020153
|
A | G | 2 | a0003c0009t0004g0009a0015c0024t0002g0012 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292+11297A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020153 | ||||||
| chr3:58020363
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.292+11507C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020363 | ||||||
| chr3:58020481
|
C | G | 1 | a0001c0030t0003g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292+11625C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020481 | ||||||
| chr3:58020481
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+11625C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020481 | ||||||
| chr3:58020539
|
G | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0045others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.292+11683G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020539 | ||||||
| chr3:58020686
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.292+11830A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020686 | ||||||
| chr3:58020719
|
GA | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.292+11879delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58020719 | |||||
| chr3:58020748
|
G | C | 6 | a0004c0006t0002g0068a0004c0006t0002g0102a0005c0010t0002g0065others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+11892G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020748 | ||||||
| chr3:58020873
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 115 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.292+12017G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58020873 | ||||||
| chr3:58021025
|
C | T | 36 | a0001c0001t0001g0047a0001c0001t0001g0132a0001c0001t0001g0137others(33): Show | 36 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.292+12169C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021025 | ||||||
| chr3:58021062
|
C | A | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+12206C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021062 | ||||||
| chr3:58021145
|
G | T | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+12289G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021145 | ||||||
| chr3:58021332
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292+12476T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021332 | ||||||
| chr3:58021372
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.292+12516T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021372 | ||||||
| chr3:58021431
|
T | G | 5 | a0001c0019t0001g0122a0002c0020t0003g0123a0003c0009t0004g0009others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+12575T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021431 | ||||||
| chr3:58021534
|
C | T | 1 | a0005c0010t0002g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292+12678C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021534 | ||||||
| chr3:58021750
|
C | G | 1 | a0002c0007t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.292+12894C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021750 | ||||||
| chr3:58021779
|
TTTTG | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+12927_292+1293 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58021779 | |||||
| chr3:58021877
|
C | T | 34 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0143others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+13021C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58021877 | ||||||
| chr3:58022366
|
T | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.292+13510T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58022366 | ||||||
| chr3:58022876
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0002g0058others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+14020G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58022876 | ||||||
| chr3:58022899
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+14043C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58022899 | ||||||
| chr3:58022904
|
G | A | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+14048G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58022904 | ||||||
| chr3:58023083
|
G | T | 1 | a0002c0002t0002g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.292+14227G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023083 | ||||||
| chr3:58023107
|
CGGCCTTT others(53): Show |
C | 1 | a0002c0012t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+14255_292+1431 others(64): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58023107 | |||||
| chr3:58023111
|
C | CT | 19 | a0001c0001t0001g0051a0001c0001t0001g0168a0001c0001t0001g0178others(16): Show | 19 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+14273dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58023111 | |||||
| chr3:58023111
|
CT | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.292+14273delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58023111 | |||||
| chr3:58023163
|
G | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.292+14307G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023163 | ||||||
| chr3:58023291
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+14435T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023291 | ||||||
| chr3:58023532
|
G | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+14676G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023532 | ||||||
| chr3:58023645
|
A | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(55): Show | 58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.292+14789A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023645 | ||||||
| chr3:58023980
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.292+15124T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023980 | ||||||
| chr3:58023982
|
A | G | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+15126A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023982 | ||||||
| chr3:58023989
|
A | G | 1 | a0002c0051t0008g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.292+15133A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58023989 | ||||||
| chr3:58024201
|
G | T | 8 | a0001c0001t0001g0178a0002c0002t0001g0176a0002c0004t0002g0170others(5): Show | 8 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+15345G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024201 | ||||||
| chr3:58024340
|
A | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+15484A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024340 | ||||||
| chr3:58024429
|
C | G | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.292+15573C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024429 | ||||||
| chr3:58024573
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.292+15717C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024573 | ||||||
| chr3:58024606
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.292+15750T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024606 | ||||||
| chr3:58024645
|
G | A | 6 | a0001c0001t0001g0047a0002c0004t0001g0156a0002c0008t0002g0155others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+15789G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024645 | ||||||
| chr3:58024701
|
C | CT | 15 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(12): Show | 15 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+15872dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTT | 6 | a0001c0001t0001g0101a0002c0002t0002g0084a0002c0002t0002g0147others(3): Show | 6 | HG01884.hp1 HG02735.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+15871_292+1587 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0045a0003c0005t0001g0100a0004c0006t0002g0068others(3): Show | 6 | HG01167.hp2 HG02602.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+15863_292+1587 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0090others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+15862_292+1587 others(15): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0085others(3): Show | 6 | HG01192.hp1 HG03017.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+15861_292+1587 others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.292+15860_292+1587 others(17): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(7): Show |
3 | a0002c0004t0002g0074a0003c0005t0001g0080a0014c0023t0001g0081 | 3 | HG04184.hp1 NA18978.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.292+15859_292+1587 others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
C | CTTTTTTT others(9): Show |
1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292+15857_292+1587 others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024701
|
CT | C | 8 | a0002c0002t0001g0176a0002c0002t0002g0160a0002c0004t0002g0170others(5): Show | 8 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+15872delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58024701 | |||||
| chr3:58024717
|
TTTTTTTT others(5): Show |
T | 8 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0059others(5): Show | 8 | HG02280.hp1 HG02630.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+15862_292+1587 others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024717 | ||||||
| chr3:58024718
|
TTTTTTTT others(4): Show |
T | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.292+15863_292+1587 others(15): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024718 | ||||||
| chr3:58024719
|
TTTTTTTT others(3): Show |
T | 1 | a0002c0004t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.292+15864_292+1587 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024719 | ||||||
| chr3:58024726
|
TTTA | T | 10 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+15871_292+1587 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024726 | ||||||
| chr3:58024729
|
A | T | 80 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.292+15873A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024729 | ||||||
| chr3:58024971
|
A | T | 4 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+16115A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024971 | ||||||
| chr3:58024990
|
C | T | 1 | a0014c0023t0001g0081 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.292+16134C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58024990 | ||||||
| chr3:58025014
|
CT | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0047others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+16176delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025014 | |||||
| chr3:58025014
|
CTT | C | 108 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.292+16175_292+1617 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025014 | |||||
| chr3:58025014
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0044t0001g0167 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.292+16162_292+1617 others(19): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025014 | |||||
| chr3:58025105
|
TC | T | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+16250delC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025105 | ||||||
| chr3:58025133
|
C | CT | 6 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121others(3): Show | 6 | HG01255.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+16291dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025133 | |||||
| chr3:58025133
|
C | CTT | 99 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.292+16290_292+1629 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025133 | |||||
| chr3:58025133
|
C | CTTT | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.292+16289_292+1629 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025133 | |||||
| chr3:58025133
|
C | CTTTT | 7 | a0001c0001t0001g0027a0002c0002t0002g0120a0002c0012t0002g0118others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+16288_292+1629 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025133 | |||||
| chr3:58025215
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.292+16359G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025215 | ||||||
| chr3:58025335
|
T | TC | 9 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(6): Show | 9 | HG01255.hp1 HG01891.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+16482dupC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58025335 | |||||
| chr3:58025602
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0002g0058a0003c0035t0003g0060others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+16746C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025602 | ||||||
| chr3:58025692
|
G | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.292+16836G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025692 | ||||||
| chr3:58025696
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.292+16840C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025696 | ||||||
| chr3:58025846
|
A | C | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+16990A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025846 | ||||||
| chr3:58025875
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.292+17019G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58025875 | ||||||
| chr3:58026034
|
G | A | 1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292+17178G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026034 | ||||||
| chr3:58026379
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+17523T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026379 | ||||||
| chr3:58026619
|
C | T | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+17763C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026619 | ||||||
| chr3:58026620
|
A | G | 4 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121others(1): Show | 4 | HG01255.hp1 HG01891.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+17764A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026620 | ||||||
| chr3:58026621
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.292+17765G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026621 | ||||||
| chr3:58026675
|
A | G | 1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292+17819A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026675 | ||||||
| chr3:58026761
|
C | T | 1 | a0004c0006t0002g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.292+17905C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026761 | ||||||
| chr3:58026924
|
C | T | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+18068C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026924 | ||||||
| chr3:58026962
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.292+18106T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58026962 | ||||||
| chr3:58027071
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.292+18215G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027071 | ||||||
| chr3:58027234
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+18378C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027234 | ||||||
| chr3:58027322
|
CT | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.292+18479delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58027322 | |||||
| chr3:58027378
|
C | T | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+18522C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027378 | ||||||
| chr3:58027471
|
G | A | 1 | a0002c0015t0001g0131 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.292+18615G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027471 | ||||||
| chr3:58027531
|
C | T | 2 | a0015c0024t0002g0012a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.292+18675C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027531 | ||||||
| chr3:58027571
|
C | G | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+18715C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027571 | ||||||
| chr3:58027742
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+18886C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027742 | ||||||
| chr3:58027846
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.292+18990C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027846 | ||||||
| chr3:58027897
|
A | G | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+19041A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027897 | ||||||
| chr3:58027955
|
T | G | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+19099T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58027955 | ||||||
| chr3:58028026
|
T | C | 1 | a0004c0006t0002g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.292+19170T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028026 | ||||||
| chr3:58028058
|
A | G | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+19202A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028058 | ||||||
| chr3:58028083
|
C | T | 6 | a0001c0001t0001g0020a0001c0053t0001g0018a0006c0017t0006g0024others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+19227C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028083 | ||||||
| chr3:58028370
|
T | TA | 10 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+19516dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58028370 | |||||
| chr3:58028533
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+19677A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028533 | ||||||
| chr3:58028562
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.292+19706G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028562 | ||||||
| chr3:58028602
|
T | A | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+19746T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028602 | ||||||
| chr3:58028608
|
TTTC | T | 5 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+19755_292+1975 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58028608 | |||||
| chr3:58028609
|
TTC | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+19755_292+1975 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58028609 | |||||
| chr3:58028611
|
C | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.292+19755C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028611 | ||||||
| chr3:58028616
|
CT | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.292+19774delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58028616 | |||||
| chr3:58028644
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+19788G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028644 | ||||||
| chr3:58028769
|
A | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(7): Show | 10 | HG01255.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+19913A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58028769 | ||||||
| chr3:58029029
|
C | G | 10 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+20173C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029029 | ||||||
| chr3:58029091
|
ATT | A | 17 | a0001c0001t0001g0137a0001c0001t0001g0179a0002c0002t0002g0125others(14): Show | 17 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+20237_292+2023 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58029091 | |||||
| chr3:58029130
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | HG02293.hp2 HG03927.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.292+20274A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029130 | ||||||
| chr3:58029151
|
T | TG | 4 | a0001c0001t0001g0059a0001c0001t0002g0058a0003c0035t0003g0060others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+20296dupG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58029151 | |||||
| chr3:58029367
|
C | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+20511C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029367 | ||||||
| chr3:58029367
|
C | T | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+20511C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029367 | ||||||
| chr3:58029506
|
C | CT | 6 | a0001c0019t0001g0122a0002c0002t0002g0125a0002c0020t0003g0123others(3): Show | 6 | HG01255.hp1 HG01891.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+20665dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58029506 | |||||
| chr3:58029522
|
G | A | 2 | a0006c0017t0006g0024a0006c0049t0002g0023 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.292+20666G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029522 | ||||||
| chr3:58029571
|
C | T | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+20715C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029571 | ||||||
| chr3:58029573
|
C | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.292+20717C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029573 | ||||||
| chr3:58029756
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.292+20900G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029756 | ||||||
| chr3:58029805
|
G | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.292+20949G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029805 | ||||||
| chr3:58029870
|
GT | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+21015delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58029870 | ||||||
| chr3:58030285
|
G | C | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292+21429G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030285 | ||||||
| chr3:58030466
|
T | C | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+21610T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030466 | ||||||
| chr3:58030523
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292+21667G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030523 | ||||||
| chr3:58030587
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.292+21731G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030587 | ||||||
| chr3:58030635
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+21779A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030635 | ||||||
| chr3:58030863
|
AAC | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+22009_292+2201 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58030863 | |||||
| chr3:58030895
|
C | T | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+22039C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030895 | ||||||
| chr3:58030989
|
G | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+22133G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58030989 | ||||||
| chr3:58031058
|
A | G | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+22202A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031058 | ||||||
| chr3:58031138
|
A | G | 1 | a0002c0012t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+22282A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031138 | ||||||
| chr3:58031149
|
G | C | 1 | a0002c0020t0003g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.292+22293G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031149 | ||||||
| chr3:58031284
|
C | T | 1 | a0004c0042t0003g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.292+22428C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031284 | ||||||
| chr3:58031384
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+22528A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031384 | ||||||
| chr3:58031387
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+22531C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031387 | ||||||
| chr3:58031409
|
A | AT | 3 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292+22559dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58031409 | |||||
| chr3:58031426
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+22570C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031426 | ||||||
| chr3:58031453
|
A | G | 5 | a0002c0003t0002g0138a0002c0003t0002g0139a0002c0003t0002g0140others(2): Show | 5 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+22597A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031453 | ||||||
| chr3:58031535
|
T | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.292+22679T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031535 | ||||||
| chr3:58031543
|
C | CT | 85 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.292+22712dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58031543 | |||||
| chr3:58031543
|
C | CTT | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.292+22711_292+2271 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58031543 | |||||
| chr3:58031543
|
C | CTTT | 11 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0059others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.292+22710_292+2271 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58031543 | |||||
| chr3:58031647
|
G | A | 2 | a0002c0004t0002g0074a0009c0028t0002g0071 | 2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.292+22791G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031647 | ||||||
| chr3:58031676
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+22820T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031676 | ||||||
| chr3:58031773
|
G | A | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.292+22917G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031773 | ||||||
| chr3:58031841
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+22985C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031841 | ||||||
| chr3:58031843
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+22987T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031843 | ||||||
| chr3:58031964
|
T | C | 2 | a0001c0001t0001g0032a0003c0005t0001g0029 | 2 | NA18988.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.292+23108T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58031964 | ||||||
| chr3:58032380
|
G | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+23524G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58032380 | ||||||
| chr3:58032593
|
A | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+23737A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58032593 | ||||||
| chr3:58032906
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+24050T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58032906 | ||||||
| chr3:58032994
|
G | A | 2 | a0006c0017t0006g0024a0006c0049t0002g0023 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.292+24138G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58032994 | ||||||
| chr3:58033023
|
A | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.292+24167A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033023 | ||||||
| chr3:58033152
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+24296C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033152 | ||||||
| chr3:58033163
|
A | T | 3 | a0002c0002t0002g0064a0002c0002t0002g0073a0018c0050t0002g0082 | 3 | HG03490.hp1 HG03834.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+24307A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033163 | ||||||
| chr3:58033221
|
C | T | 3 | a0004c0006t0002g0068a0004c0006t0002g0102a0005c0010t0002g0065 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.292+24365C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033221 | ||||||
| chr3:58033229
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.292+24373C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033229 | ||||||
| chr3:58033342
|
G | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.292+24486G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033342 | ||||||
| chr3:58033396
|
TTG | T | 10 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0059others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+24542_292+2454 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58033396 | |||||
| chr3:58033397
|
TG | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.292+24542delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033397 | ||||||
| chr3:58033398
|
G | T | 3 | a0002c0015t0001g0131a0012c0055t0001g0010a0014c0023t0001g0081 | 3 | HG01167.hp1 HG02055.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.292+24542G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033398 | ||||||
| chr3:58033552
|
T | C | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+24696T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033552 | ||||||
| chr3:58033720
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+24864T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033720 | ||||||
| chr3:58033826
|
A | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+24970A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033826 | ||||||
| chr3:58033853
|
G | A | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+24997G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033853 | ||||||
| chr3:58033906
|
G | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 44 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.292+25050G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033906 | ||||||
| chr3:58033910
|
G | A | 29 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0146others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.292+25054G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58033910 | ||||||
| chr3:58034150
|
C | T | 3 | a0001c0019t0001g0122a0002c0020t0003g0123a0004c0021t0001g0121 | 3 | HG01255.hp1 HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+25294C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034150 | ||||||
| chr3:58034153
|
G | A | 6 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(3): Show | 6 | HG01257.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+25297G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034153 | ||||||
| chr3:58034160
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.292+25304C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034160 | ||||||
| chr3:58034175
|
T | G | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.292+25319T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034175 | ||||||
| chr3:58034226
|
A | G | 2 | a0015c0024t0002g0012a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.292+25370A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034226 | ||||||
| chr3:58034268
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+25412C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034268 | ||||||
| chr3:58034400
|
AT | A | 17 | a0001c0001t0001g0087a0001c0019t0001g0122a0002c0002t0002g0126others(14): Show | 17 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+25559delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58034400 | |||||
| chr3:58034568
|
A | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0002g0058others(2): Show | 5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+25712A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034568 | ||||||
| chr3:58034873
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.292+26017C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58034873 | ||||||
| chr3:58035046
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0002g0058a0003c0035t0003g0060others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+26190G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58035046 | ||||||
| chr3:58035099
|
T | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.292+26243T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58035099 | ||||||
| chr3:58035147
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0002g0058a0003c0035t0003g0060others(1): Show | 4 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+26291C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58035147 | ||||||
| chr3:58035273
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.292+26417G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58035273 | ||||||
| chr3:58035940
|
C | T | 3 | a0002c0002t0002g0120a0002c0012t0002g0118a0005c0011t0003g0119 | 3 | HG03209.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.292+27084C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58035940 | ||||||
| chr3:58036448
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.292+27592G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036448 | ||||||
| chr3:58036494
|
CA | C | 5 | a0001c0001t0001g0059a0001c0001t0002g0058a0002c0020t0003g0123others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+27639delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036494 | ||||||
| chr3:58036563
|
C | T | 1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292+27707C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036563 | ||||||
| chr3:58036671
|
T | A | 6 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+27815T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036671 | ||||||
| chr3:58036705
|
A | G | 1 | a0002c0008t0002g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.292+27849A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036705 | ||||||
| chr3:58036900
|
A | G | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+28044A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58036900 | ||||||
| chr3:58037034
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.292+28178T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037034 | ||||||
| chr3:58037058
|
C | CT | 11 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0032others(8): Show | 11 | HG01106.hp1 HG01123.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+28228dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58037058 | |||||
| chr3:58037058
|
CT | C | 12 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0079others(9): Show | 12 | HG01169.hp1 HG01516.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+28228delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58037058 | |||||
| chr3:58037058
|
CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(9): Show | 12 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+28218_292+2822 others(15): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58037058 | |||||
| chr3:58037099
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+28243C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037099 | ||||||
| chr3:58037184
|
C | T | 1 | a0002c0020t0003g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.292+28328C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037184 | ||||||
| chr3:58037370
|
C | T | 3 | a0015c0024t0002g0012a0020c0052t0001g0117a0026c0038t0002g0158 | 3 | HG02630.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.292+28514C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037370 | ||||||
| chr3:58037416
|
A | T | 2 | a0001c0001t0001g0146a0001c0031t0005g0145 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.292+28560A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037416 | ||||||
| chr3:58037452
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+28596C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037452 | ||||||
| chr3:58037476
|
C | T | 2 | a0005c0010t0003g0002a0005c0048t0005g0001 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+28620C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58037476 | ||||||
| chr3:58037928
|
T | TA | 5 | a0001c0001t0001g0059a0001c0001t0002g0058a0002c0020t0003g0123others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+29078dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58037928 | |||||
| chr3:58038014
|
ATTGT | A | 3 | a0001c0019t0001g0122a0004c0021t0001g0121a0012c0055t0001g0010 | 3 | HG01255.hp1 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+29185_292+2918 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58038014 | |||||
| chr3:58038014
|
ATTGTTTG others(1): Show |
A | 2 | a0015c0024t0002g0012a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.292+29181_292+2918 others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58038014 | |||||
| chr3:58038021
|
G | T | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+29165G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038021 | ||||||
| chr3:58038071
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.292+29215C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038071 | ||||||
| chr3:58038100
|
G | T | 6 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+29244G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038100 | ||||||
| chr3:58038179
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.292+29323G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038179 | ||||||
| chr3:58038248
|
C | T | 1 | a0002c0012t0002g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292+29392C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038248 | ||||||
| chr3:58038308
|
C | T | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.292+29452C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038308 | ||||||
| chr3:58038426
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.292+29570T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038426 | ||||||
| chr3:58038440
|
C | CT | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.292+29596dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58038440 | |||||
| chr3:58038580
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.292+29724A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038580 | ||||||
| chr3:58038595
|
A | AT | 6 | a0001c0001t0002g0021a0001c0001t0002g0098a0001c0001t0002g0099others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+29754dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58038595 | |||||
| chr3:58038780
|
C | T | 3 | a0001c0001t0001g0151a0002c0012t0002g0152a0005c0037t0003g0129 | 3 | HG01884.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.292+29924C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038780 | ||||||
| chr3:58038868
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+30012C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038868 | ||||||
| chr3:58038874
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292+30018A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038874 | ||||||
| chr3:58038963
|
A | C | 1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.292+30107A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038963 | ||||||
| chr3:58038971
|
A | T | 3 | a0001c0019t0001g0122a0004c0021t0001g0121a0012c0055t0001g0010 | 3 | HG01255.hp1 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+30115A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58038971 | ||||||
| chr3:58039022
|
CT | C | 15 | a0001c0001t0001g0059a0001c0001t0001g0079a0001c0001t0001g0097others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+30183delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58039022 | |||||
| chr3:58039038
|
T | A | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+30182T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039038 | ||||||
| chr3:58039039
|
T | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.292+30183T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039039 | ||||||
| chr3:58039040
|
A | T | 4 | a0001c0001t0001g0014a0002c0004t0001g0156a0002c0008t0002g0155others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+30184A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039040 | ||||||
| chr3:58039058
|
C | T | 3 | a0002c0002t0002g0064a0002c0002t0002g0073a0018c0050t0002g0082 | 3 | HG03490.hp1 HG03834.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+30202C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039058 | ||||||
| chr3:58039063
|
T | C | 1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.292+30207T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039063 | ||||||
| chr3:58039071
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+30215C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039071 | ||||||
| chr3:58039196
|
GA | G | 9 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+30355delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58039196 | |||||
| chr3:58039198
|
A | C | 7 | a0001c0001t0001g0059a0001c0001t0002g0058a0001c0014t0001g0111others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+30342A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039198 | ||||||
| chr3:58039310
|
T | TA | 19 | a0001c0001t0001g0059a0001c0001t0001g0090a0002c0002t0002g0124others(16): Show | 19 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.292+30469dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58039310 | |||||
| chr3:58039310
|
TA | T | 8 | a0001c0001t0001g0020a0001c0014t0001g0111a0002c0007t0002g0164others(5): Show | 8 | HG01358.hp1 HG02109.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+30469delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58039310 | |||||
| chr3:58039373
|
G | A | 3 | a0001c0019t0001g0122a0004c0021t0001g0121a0012c0055t0001g0010 | 3 | HG01255.hp1 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+30517G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039373 | ||||||
| chr3:58039455
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.292+30599C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039455 | ||||||
| chr3:58039724
|
T | G | 14 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.292+30868T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039724 | ||||||
| chr3:58039786
|
G | A | 6 | a0001c0001t0002g0058a0001c0014t0001g0111a0002c0020t0003g0123others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+30930G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039786 | ||||||
| chr3:58039870
|
T | C | 6 | a0001c0001t0002g0058a0001c0014t0001g0111a0002c0020t0003g0123others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+31014T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58039870 | ||||||
| chr3:58040176
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.292+31320C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040176 | ||||||
| chr3:58040210
|
C | G | 1 | a0022c0040t0001g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.292+31354C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040210 | ||||||
| chr3:58040214
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292+31358C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040214 | ||||||
| chr3:58040412
|
G | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+31556G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040412 | ||||||
| chr3:58040473
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+31617G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040473 | ||||||
| chr3:58040556
|
C | A | 9 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+31700C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040556 | ||||||
| chr3:58040617
|
C | T | 1 | a0002c0002t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292+31761C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040617 | ||||||
| chr3:58040646
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(69): Show | 72 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.292+31790T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58040646 | ||||||
| chr3:58041180
|
G | C | 2 | a0002c0002t0002g0160a0002c0002t0002g0163 | 2 | HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.292+32324G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041180 | ||||||
| chr3:58041205
|
A | T | 1 | a0005c0011t0003g0011 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292+32349A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041205 | ||||||
| chr3:58041237
|
C | T | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292+32381C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041237 | ||||||
| chr3:58041241
|
A | G | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292+32385A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041241 | ||||||
| chr3:58041470
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.292+32614A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041470 | ||||||
| chr3:58041472
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.292+32616G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041472 | ||||||
| chr3:58041581
|
C | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.292+32725C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041581 | ||||||
| chr3:58041677
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.292+32821T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041677 | ||||||
| chr3:58041809
|
C | T | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+32953C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041809 | ||||||
| chr3:58041825
|
C | T | 3 | a0001c0019t0001g0122a0004c0021t0001g0121a0012c0055t0001g0010 | 3 | HG01255.hp1 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.292+32969C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041825 | ||||||
| chr3:58041873
|
G | C | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+33017G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58041873 | ||||||
| chr3:58042345
|
G | GT | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.292+33508dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58042345 | |||||
| chr3:58042345
|
GT | G | 7 | a0001c0001t0001g0086a0001c0001t0001g0107a0002c0002t0002g0126others(4): Show | 7 | HG01167.hp1 HG01975.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+33508delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58042345 | |||||
| chr3:58042364
|
T | TA | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+33511dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58042364 | |||||
| chr3:58042365
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+33509A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042365 | ||||||
| chr3:58042398
|
G | A | 24 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0002g0058others(21): Show | 24 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+33542G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042398 | ||||||
| chr3:58042429
|
C | T | 1 | a0004c0042t0003g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.292+33573C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042429 | ||||||
| chr3:58042440
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0002g0058a0002c0015t0003g0025others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+33584C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042440 | ||||||
| chr3:58042625
|
C | T | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+33769C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042625 | ||||||
| chr3:58042739
|
G | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+33883G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042739 | ||||||
| chr3:58042792
|
C | T | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292+33936C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042792 | ||||||
| chr3:58042965
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-34081G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58042965 | ||||||
| chr3:58043141
|
C | CT | 7 | a0002c0004t0001g0156a0002c0008t0002g0155a0004c0006t0002g0048others(4): Show | 7 | HG01167.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-33882dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58043141 | |||||
| chr3:58043141
|
C | CTT | 13 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(10): Show | 13 | HG01169.hp1 HG01257.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-33883_293-3388 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58043141 | |||||
| chr3:58043141
|
CT | C | 63 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0040others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.293-33882delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58043141 | |||||
| chr3:58043146
|
T | G | 30 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0146others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-33900T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043146 | ||||||
| chr3:58043189
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-33857C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043189 | ||||||
| chr3:58043190
|
G | C | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.293-33856G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043190 | ||||||
| chr3:58043289
|
C | T | 30 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0146others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-33757C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043289 | ||||||
| chr3:58043537
|
G | T | 3 | a0002c0002t0002g0006a0002c0002t0002g0120a0002c0012t0002g0118 | 3 | HG02896.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.293-33509G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043537 | ||||||
| chr3:58043715
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-33331G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043715 | ||||||
| chr3:58043730
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.293-33316C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043730 | ||||||
| chr3:58043778
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-33268A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043778 | ||||||
| chr3:58043790
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293-33256C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043790 | ||||||
| chr3:58043883
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-33163C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58043883 | ||||||
| chr3:58044257
|
C | T | 16 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-32789C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58044257 | ||||||
| chr3:58044270
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.293-32776G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58044270 | ||||||
| chr3:58044337
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-32709C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58044337 | ||||||
| chr3:58044436
|
A | AAAAC | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.293-32593_293-3259 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58044436 | |||||
| chr3:58044558
|
G | A | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.293-32488G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58044558 | ||||||
| chr3:58044638
|
T | A | 8 | a0001c0001t0001g0027a0001c0001t0002g0058a0001c0014t0001g0111others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-32408T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58044638 | ||||||
| chr3:58045264
|
A | G | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.293-31782A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045264 | ||||||
| chr3:58045397
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.293-31649A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045397 | ||||||
| chr3:58045434
|
C | G | 14 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-31612C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045434 | ||||||
| chr3:58045473
|
TG | T | 4 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-31572delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045473 | ||||||
| chr3:58045474
|
G | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0002g0058others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-31572G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045474 | ||||||
| chr3:58045657
|
CT | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0002g0058others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-31387delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58045657 | |||||
| chr3:58045861
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-31185G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045861 | ||||||
| chr3:58045873
|
G | A | 2 | a0001c0001t0001g0146a0001c0031t0005g0145 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.293-31173G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58045873 | ||||||
| chr3:58045999
|
C | CA | 21 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-31022dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58045999 | |||||
| chr3:58045999
|
CA | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.293-31022delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58045999 | |||||
| chr3:58045999
|
CAAAAA | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-31026_293-3102 others(9): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58045999 | |||||
| chr3:58046185
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.293-30861A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58046185 | ||||||
| chr3:58046340
|
A | T | 3 | a0001c0019t0001g0122a0004c0021t0001g0121a0012c0055t0001g0010 | 3 | HG01255.hp1 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.293-30706A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58046340 | ||||||
| chr3:58046368
|
C | T | 10 | a0001c0001t0001g0020a0001c0053t0001g0018a0002c0008t0014g0110others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-30678C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58046368 | ||||||
| chr3:58046455
|
G | GT | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.293-30578dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58046455 | |||||
| chr3:58046553
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.293-30493G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58046553 | ||||||
| chr3:58046793
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0105a0009c0034t0002g0104 | 3 | HG01123.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.293-30253C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58046793 | ||||||
| chr3:58047496
|
G | C | 1 | a0005c0037t0003g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293-29550G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047496 | ||||||
| chr3:58047665
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.293-29381C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047665 | ||||||
| chr3:58047676
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.293-29370C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047676 | ||||||
| chr3:58047821
|
C | G | 4 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-29225C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047821 | ||||||
| chr3:58047883
|
A | G | 1 | a0003c0009t0004g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.293-29163A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047883 | ||||||
| chr3:58047974
|
C | G | 31 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0146others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.293-29072C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58047974 | ||||||
| chr3:58048099
|
G | A | 5 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0041t0001g0016others(2): Show | 5 | HG02818.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-28947G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048099 | ||||||
| chr3:58048107
|
A | T | 31 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0146others(28): Show | 31 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.293-28939A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048107 | ||||||
| chr3:58048250
|
G | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.293-28796G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048250 | ||||||
| chr3:58048393
|
G | A | 3 | a0001c0001t0001g0014a0005c0010t0002g0013a0005c0011t0003g0011 | 3 | HG02559.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293-28653G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048393 | ||||||
| chr3:58048605
|
C | T | 3 | a0001c0001t0001g0014a0005c0010t0002g0013a0005c0011t0003g0011 | 3 | HG02559.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293-28441C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048605 | ||||||
| chr3:58048863
|
G | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0002g0058others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-28183G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58048863 | ||||||
| chr3:58049038
|
T | C | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-28008T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58049038 | ||||||
| chr3:58049420
|
T | C | 1 | a0002c0051t0008g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.293-27626T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58049420 | ||||||
| chr3:58049770
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(34): Show | 37 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.293-27276G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58049770 | ||||||
| chr3:58049820
|
G | A | 3 | a0007c0016t0004g0095a0007c0016t0004g0096a0021c0047t0004g0093 | 3 | HG02451.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-27226G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58049820 | ||||||
| chr3:58049827
|
T | A | 14 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-27219T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58049827 | ||||||
| chr3:58050021
|
CT | C | 88 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.293-27008delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58050021 | |||||
| chr3:58050021
|
CTT | C | 24 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(21): Show | 24 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-27009_293-2700 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58050021 | |||||
| chr3:58050266
|
T | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-26780T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050266 | ||||||
| chr3:58050284
|
T | C | 1 | a0002c0002t0002g0073 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.293-26762T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050284 | ||||||
| chr3:58050621
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-26425G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050621 | ||||||
| chr3:58050688
|
C | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-26358C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050688 | ||||||
| chr3:58050699
|
A | G | 2 | a0015c0024t0002g0012a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.293-26347A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050699 | ||||||
| chr3:58050801
|
G | T | 3 | a0001c0001t0001g0027a0002c0015t0003g0025a0003c0009t0004g0026 | 3 | HG01109.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.293-26245G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050801 | ||||||
| chr3:58050924
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.293-26122T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58050924 | ||||||
| chr3:58051045
|
T | C | 2 | a0015c0024t0002g0012a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.293-26001T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051045 | ||||||
| chr3:58051065
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.293-25981C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051065 | ||||||
| chr3:58051084
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.293-25962A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051084 | ||||||
| chr3:58051208
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.293-25838T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051208 | ||||||
| chr3:58051235
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.293-25811C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051235 | ||||||
| chr3:58051372
|
C | T | 1 | a0002c0002t0002g0006 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.293-25674C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051372 | ||||||
| chr3:58051675
|
GT | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.293-25364delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58051675 | |||||
| chr3:58051684
|
G | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.293-25362G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051684 | ||||||
| chr3:58051685
|
G | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.293-25361G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051685 | ||||||
| chr3:58051760
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-25286A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051760 | ||||||
| chr3:58051776
|
G | A | 1 | a0002c0002t0002g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-25270G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051776 | ||||||
| chr3:58051814
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-25232C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051814 | ||||||
| chr3:58051850
|
G | C | 2 | a0001c0001t0001g0146a0001c0031t0005g0145 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.293-25196G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051850 | ||||||
| chr3:58051851
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-25195T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58051851 | ||||||
| chr3:58052004
|
A | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-25042A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052004 | ||||||
| chr3:58052016
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-25030G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052016 | ||||||
| chr3:58052036
|
G | A | 3 | a0002c0002t0002g0064a0002c0002t0002g0073a0018c0050t0002g0082 | 3 | HG03490.hp1 HG03834.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.293-25010G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052036 | ||||||
| chr3:58052145
|
A | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-24901A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052145 | ||||||
| chr3:58052163
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-24883T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052163 | ||||||
| chr3:58052212
|
C | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-24834C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052212 | ||||||
| chr3:58052472
|
G | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-24574G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052472 | ||||||
| chr3:58052540
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.293-24506A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052540 | ||||||
| chr3:58052615
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.293-24431C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052615 | ||||||
| chr3:58052616
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0053others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.293-24430G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052616 | ||||||
| chr3:58052641
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.293-24405C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052641 | ||||||
| chr3:58052791
|
G | A | 1 | a0005c0011t0004g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.293-24255G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052791 | ||||||
| chr3:58052819
|
C | A | 80 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.293-24227C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052819 | ||||||
| chr3:58052878
|
C | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-24168C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052878 | ||||||
| chr3:58052944
|
G | T | 2 | a0001c0001t0001g0179a0002c0002t0002g0148 | 2 | HG01884.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.293-24102G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58052944 | ||||||
| chr3:58053029
|
T | C | 1 | a0004c0042t0003g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293-24017T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053029 | ||||||
| chr3:58053650
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.293-23396G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053650 | ||||||
| chr3:58053690
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-23356C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053690 | ||||||
| chr3:58053731
|
G | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0027others(15): Show | 18 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-23315G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053731 | ||||||
| chr3:58053855
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293-23191G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053855 | ||||||
| chr3:58053861
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-23185C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053861 | ||||||
| chr3:58053955
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.293-23091C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053955 | ||||||
| chr3:58053986
|
G | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.293-23060G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58053986 | ||||||
| chr3:58054078
|
A | C | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-22968A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054078 | ||||||
| chr3:58054095
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.293-22951G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054095 | ||||||
| chr3:58054116
|
C | G | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-22930C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054116 | ||||||
| chr3:58054170
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-22876A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054170 | ||||||
| chr3:58054299
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-22747T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054299 | ||||||
| chr3:58054560
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.293-22486A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054560 | ||||||
| chr3:58054662
|
C | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-22384C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054662 | ||||||
| chr3:58054741
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-22305T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054741 | ||||||
| chr3:58054906
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-22140T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054906 | ||||||
| chr3:58054907
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-22139G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58054907 | ||||||
| chr3:58055064
|
C | T | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-21982C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055064 | ||||||
| chr3:58055109
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-21937A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055109 | ||||||
| chr3:58055173
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-21873C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055173 | ||||||
| chr3:58055267
|
C | CA | 25 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0137others(22): Show | 25 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.293-21767dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58055267 | |||||
| chr3:58055267
|
C | CAA | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-21768_293-2176 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58055267 | |||||
| chr3:58055338
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-21708G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055338 | ||||||
| chr3:58055630
|
A | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-21416A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055630 | ||||||
| chr3:58055904
|
G | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-21142G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055904 | ||||||
| chr3:58055910
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-21136C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055910 | ||||||
| chr3:58055967
|
A | G | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.293-21079A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055967 | ||||||
| chr3:58055979
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-21067A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58055979 | ||||||
| chr3:58056073
|
T | TTTTA | 7 | a0001c0001t0001g0033a0001c0001t0001g0151a0002c0002t0002g0006others(4): Show | 7 | HG00438.hp1 HG01884.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-20941_293-2093 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58056073 | |||||
| chr3:58056089
|
ATTTATTT others(16): Show |
A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-20953_293-2093 others(27): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58056089 | |||||
| chr3:58056101
|
A | T | 1 | a0002c0008t0014g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.293-20945A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056101 | ||||||
| chr3:58056105
|
A | AT | 7 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG01109.hp2 HG01169.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-20927dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58056105 | |||||
| chr3:58056105
|
A | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0062others(7): Show | 10 | HG00408.hp2 HG02300.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-20941A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056105 | ||||||
| chr3:58056109
|
T | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0097others(48): Show | 51 | HG00280.hp1 HG00738.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.293-20937T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056109 | ||||||
| chr3:58056110
|
T | A | 3 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0172 | 3 | HG02630.hp2 HG02735.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.293-20936T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056110 | ||||||
| chr3:58056163
|
A | G | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-20883A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056163 | ||||||
| chr3:58056173
|
C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(51): Show | 54 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.293-20873C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056173 | ||||||
| chr3:58056246
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-20800C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056246 | ||||||
| chr3:58056314
|
G | A | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-20732G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056314 | ||||||
| chr3:58056347
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-20699T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056347 | ||||||
| chr3:58056357
|
TC | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0002g0058others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-20686delC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58056357 | |||||
| chr3:58056602
|
A | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-20444A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056602 | ||||||
| chr3:58056687
|
C | T | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-20359C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056687 | ||||||
| chr3:58056715
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-20331C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58056715 | ||||||
| chr3:58057243
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19803C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057243 | ||||||
| chr3:58057267
|
A | T | 2 | a0003c0005t0001g0043a0003c0005t0001g0044 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.293-19779A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057267 | ||||||
| chr3:58057345
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19701A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057345 | ||||||
| chr3:58057412
|
A | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-19634A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057412 | ||||||
| chr3:58057421
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0002g0058a0002c0015t0003g0025others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-19625T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057421 | ||||||
| chr3:58057447
|
T | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19599T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057447 | ||||||
| chr3:58057462
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19584A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057462 | ||||||
| chr3:58057522
|
G | GCTTAGAT others(7): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19523_293-1952 others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58057522 | |||||
| chr3:58057542
|
T | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19504T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057542 | ||||||
| chr3:58057546
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.293-19500A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057546 | ||||||
| chr3:58057846
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.293-19200A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057846 | ||||||
| chr3:58057876
|
C | T | 5 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-19170C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057876 | ||||||
| chr3:58057894
|
G | A | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-19152G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057894 | ||||||
| chr3:58057909
|
G | C | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-19137G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057909 | ||||||
| chr3:58057940
|
G | A | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-19106G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58057940 | ||||||
| chr3:58058019
|
C | T | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-19027C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058019 | ||||||
| chr3:58058040
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-19006T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058040 | ||||||
| chr3:58058104
|
T | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-18942T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058104 | ||||||
| chr3:58058206
|
A | C | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-18840A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058206 | ||||||
| chr3:58058256
|
G | A | 1 | a0002c0008t0002g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.293-18790G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058256 | ||||||
| chr3:58058273
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-18773C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058273 | ||||||
| chr3:58058293
|
T | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-18753T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058293 | ||||||
| chr3:58058298
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-18748G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058298 | ||||||
| chr3:58058445
|
T | TGCCATTA others(3): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-18599_293-1859 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58058445 | |||||
| chr3:58058459
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0002g0058others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-18587C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058459 | ||||||
| chr3:58058486
|
G | A | 2 | a0001c0001t0001g0179a0002c0002t0002g0148 | 2 | HG01884.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.293-18560G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058486 | ||||||
| chr3:58058961
|
T | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-18085T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58058961 | ||||||
| chr3:58059189
|
A | C | 1 | a0023c0033t0001g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.293-17857A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059189 | ||||||
| chr3:58059247
|
C | G | 7 | a0001c0001t0001g0027a0001c0001t0002g0058a0002c0015t0003g0025others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-17799C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059247 | ||||||
| chr3:58059427
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0047others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-17619A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059427 | ||||||
| chr3:58059517
|
C | T | 1 | a0002c0008t0002g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.293-17529C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059517 | ||||||
| chr3:58059552
|
G | A | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-17494G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059552 | ||||||
| chr3:58059560
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(51): Show | 54 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.293-17486C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059560 | ||||||
| chr3:58059562
|
T | C | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-17484T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059562 | ||||||
| chr3:58059589
|
T | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0027others(14): Show | 17 | HG01109.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-17457T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059589 | ||||||
| chr3:58059590
|
G | A | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-17456G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059590 | ||||||
| chr3:58059634
|
G | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-17412G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059634 | ||||||
| chr3:58059791
|
T | C | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.293-17255T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059791 | ||||||
| chr3:58059811
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(56): Show | 59 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.293-17235C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059811 | ||||||
| chr3:58059854
|
T | C | 5 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-17192T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58059854 | ||||||
| chr3:58060038
|
T | C | 1 | a0002c0002t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-17008T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060038 | ||||||
| chr3:58060192
|
G | GT | 5 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-16848dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060192 | |||||
| chr3:58060352
|
C | CTT | 6 | a0002c0004t0001g0156a0002c0008t0002g0155a0003c0009t0004g0009others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-16676_293-1667 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060352 | |||||
| chr3:58060352
|
CT | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(50): Show | 53 | HG00280.hp2 HG00408.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.293-16675delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060352 | |||||
| chr3:58060352
|
CTT | C | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-16676_293-1667 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060352 | |||||
| chr3:58060354
|
T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 61 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.293-16692T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060354 | ||||||
| chr3:58060355
|
T | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0045others(50): Show | 53 | HG00280.hp2 HG00408.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.293-16691T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060355 | ||||||
| chr3:58060394
|
C | T | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-16652C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060394 | ||||||
| chr3:58060447
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-16599G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060447 | ||||||
| chr3:58060769
|
CAAA | C | 16 | a0001c0001t0001g0045a0001c0001t0001g0091a0001c0001t0001g0179others(13): Show | 16 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-16249_293-1624 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060769 | |||||
| chr3:58060769
|
CAAAA | C | 70 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0053others(67): Show | 70 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.293-16250_293-1624 others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060769 | |||||
| chr3:58060784
|
AAAAAAAA others(9): Show |
A | 7 | a0001c0001t0001g0027a0001c0001t0002g0058a0002c0015t0003g0025others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-16258_293-1624 others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060784 | |||||
| chr3:58060786
|
AAAAAAAA others(7): Show |
A | 2 | a0004c0006t0002g0068a0004c0006t0002g0102 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.293-16256_293-1624 others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060786 | |||||
| chr3:58060787
|
AAAAAAAA others(6): Show |
A | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(47): Show | 50 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.293-16255_293-1624 others(17): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060787 | |||||
| chr3:58060788
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0061a0002c0004t0002g0074a0016c0025t0010g0031 | 3 | HG04184.hp1 NA18957.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.293-16254_293-1624 others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060788 | |||||
| chr3:58060796
|
A | G | 7 | a0001c0001t0001g0047a0001c0001t0003g0089a0001c0014t0001g0115others(4): Show | 7 | HG02451.hp2 HG03225.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-16250A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060796 | ||||||
| chr3:58060800
|
GAAAGAAA others(2): Show |
G | 5 | a0001c0001t0003g0089a0001c0014t0001g0115a0007c0016t0004g0095others(2): Show | 5 | HG02451.hp2 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-16238_293-1623 others(13): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060800 | |||||
| chr3:58060804
|
GAAAGAAA others(3): Show |
G | 1 | a0002c0002t0002g0165 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.293-16223_293-1621 others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060804 | |||||
| chr3:58060808
|
GA | G | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.293-16234delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58060808 | |||||
| chr3:58060888
|
G | A | 4 | a0001c0001t0001g0003a0003c0005t0001g0080a0003c0005t0001g0100others(1): Show | 4 | HG02630.hp2 HG02735.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-16158G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060888 | ||||||
| chr3:58060938
|
G | A | 3 | a0005c0010t0003g0002a0005c0048t0005g0001a0006c0049t0002g0023 | 3 | HG02559.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-16108G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58060938 | ||||||
| chr3:58061102
|
C | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-15944C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061102 | ||||||
| chr3:58061115
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.293-15931G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061115 | ||||||
| chr3:58061222
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.293-15824A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061222 | ||||||
| chr3:58061278
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.293-15768T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061278 | ||||||
| chr3:58061516
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(52): Show | 55 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.293-15530C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061516 | ||||||
| chr3:58061590
|
G | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0002g0058others(15): Show | 18 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-15456G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061590 | ||||||
| chr3:58061591
|
G | A | 1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.293-15455G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061591 | ||||||
| chr3:58061745
|
G | A | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.293-15301G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061745 | ||||||
| chr3:58061750
|
CAA | C | 5 | a0001c0001t0001g0014a0001c0014t0001g0111a0005c0010t0002g0013others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-15281_293-1528 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58061750 | |||||
| chr3:58061806
|
G | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0105a0003c0005t0001g0029others(1): Show | 4 | HG01123.hp2 HG02004.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-15240G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061806 | ||||||
| chr3:58061821
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-15225G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061821 | ||||||
| chr3:58061861
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.293-15185G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58061861 | ||||||
| chr3:58062335
|
G | A | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-14711G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58062335 | ||||||
| chr3:58062546
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(60): Show | 63 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.293-14500G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58062546 | ||||||
| chr3:58062608
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.293-14438A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58062608 | ||||||
| chr3:58062955
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.293-14091C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58062955 | ||||||
| chr3:58062972
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(51): Show | 54 | HG01109.hp1 HG01109.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.293-14074A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58062972 | ||||||
| chr3:58063037
|
G | C | 1 | a0003c0009t0004g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.293-14009G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063037 | ||||||
| chr3:58063044
|
G | A | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-14002G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063044 | ||||||
| chr3:58063283
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.293-13763C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063283 | ||||||
| chr3:58063449
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0059others(7): Show | 10 | HG02040.hp2 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-13597G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063449 | ||||||
| chr3:58063664
|
A | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-13382A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063664 | ||||||
| chr3:58063912
|
G | A | 41 | a0001c0001t0001g0027a0001c0001t0001g0137a0001c0001t0001g0146others(38): Show | 41 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.293-13134G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58063912 | ||||||
| chr3:58064031
|
A | C | 1 | a0002c0002t0002g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-13015A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064031 | ||||||
| chr3:58064036
|
C | T | 4 | a0001c0014t0001g0111a0001c0014t0001g0115a0004c0006t0012g0109others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-13010C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064036 | ||||||
| chr3:58064164
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-12882A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064164 | ||||||
| chr3:58064251
|
C | T | 40 | a0001c0001t0001g0027a0001c0001t0001g0137a0001c0001t0001g0146others(37): Show | 40 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.293-12795C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064251 | ||||||
| chr3:58064538
|
C | T | 40 | a0001c0001t0001g0027a0001c0001t0001g0137a0001c0001t0001g0146others(37): Show | 40 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.293-12508C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064538 | ||||||
| chr3:58064893
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.293-12153G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064893 | ||||||
| chr3:58064995
|
G | A | 4 | a0001c0001t0001g0151a0002c0012t0002g0118a0002c0012t0002g0152others(1): Show | 4 | HG01884.hp1 HG03209.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-12051G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58064995 | ||||||
| chr3:58065130
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.293-11916T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065130 | ||||||
| chr3:58065159
|
G | A | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-11887G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065159 | ||||||
| chr3:58065221
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-11825A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065221 | ||||||
| chr3:58065308
|
G | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0047a0001c0001t0001g0051others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-11738G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065308 | ||||||
| chr3:58065389
|
C | T | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.293-11657C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065389 | ||||||
| chr3:58065568
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0076others(3): Show | 6 | HG02040.hp2 HG02630.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-11478A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065568 | ||||||
| chr3:58065580
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-11466G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065580 | ||||||
| chr3:58065813
|
A | G | 14 | a0001c0001t0001g0027a0001c0001t0001g0146a0001c0001t0002g0058others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-11233A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58065813 | ||||||
| chr3:58066217
|
C | CT | 33 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0027others(30): Show | 33 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.293-10815dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58066217 | |||||
| chr3:58066280
|
C | T | 1 | a0002c0002t0002g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-10766C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066280 | ||||||
| chr3:58066324
|
A | G | 2 | a0002c0002t0002g0147a0002c0002t0002g0150 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.293-10722A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066324 | ||||||
| chr3:58066368
|
C | T | 1 | a0001c0031t0005g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-10678C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066368 | ||||||
| chr3:58066390
|
T | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.293-10656T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066390 | ||||||
| chr3:58066418
|
C | T | 1 | a0001c0026t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.293-10628C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066418 | ||||||
| chr3:58066637
|
A | G | 2 | a0002c0004t0001g0156a0005c0010t0002g0013 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.293-10409A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066637 | ||||||
| chr3:58066741
|
G | T | 2 | a0003c0005t0001g0043a0003c0005t0001g0044 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.293-10305G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066741 | ||||||
| chr3:58066907
|
G | A | 26 | a0001c0001t0001g0034a0001c0001t0001g0137a0001c0001t0001g0151others(23): Show | 26 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.293-10139G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58066907 | ||||||
| chr3:58067191
|
CT | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(79): Show | 82 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.293-9843delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58067191 | |||||
| chr3:58067250
|
AGCACCAC others(2): Show |
A | 14 | a0001c0001t0001g0027a0001c0001t0001g0146a0001c0001t0002g0058others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-9794_293-9786d others(11): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58067250 | |||||
| chr3:58067305
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.293-9741G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067305 | ||||||
| chr3:58067445
|
C | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.293-9601C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067445 | ||||||
| chr3:58067544
|
A | G | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.293-9502A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067544 | ||||||
| chr3:58067554
|
A | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0053t0001g0018others(4): Show | 7 | HG02615.hp2 HG02922.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-9492A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067554 | ||||||
| chr3:58067572
|
G | GT | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(88): Show | 91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.293-9466dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58067572 | |||||
| chr3:58067581
|
G | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(90): Show | 93 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.293-9465G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067581 | ||||||
| chr3:58067585
|
G | T | 2 | a0003c0009t0004g0009a0003c0009t0004g0017 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.293-9461G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067585 | ||||||
| chr3:58067593
|
G | T | 2 | a0003c0009t0004g0009a0003c0009t0004g0017 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.293-9453G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067593 | ||||||
| chr3:58067596
|
T | G | 2 | a0003c0009t0004g0009a0003c0009t0004g0017 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.293-9450T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067596 | ||||||
| chr3:58067602
|
TTG | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(86): Show | 89 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.293-9442_293-9441d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58067602 | |||||
| chr3:58067605
|
T | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(86): Show | 89 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.293-9441T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067605 | ||||||
| chr3:58067682
|
C | T | 27 | a0001c0001t0001g0045a0001c0001t0001g0137a0001c0001t0001g0151others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-9364C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067682 | ||||||
| chr3:58067698
|
G | A | 33 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 33 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-9348G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067698 | ||||||
| chr3:58067721
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.293-9325T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067721 | ||||||
| chr3:58067877
|
A | G | 1 | a0003c0005t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.293-9169A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58067877 | ||||||
| chr3:58068280
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.293-8766G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58068280 | ||||||
| chr3:58068426
|
A | C | 24 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(21): Show | 24 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-8620A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58068426 | ||||||
| chr3:58068616
|
G | GT | 27 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-8430_293-8429i others(3): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58068616 | ||||||
| chr3:58069032
|
A | G | 23 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-8014A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069032 | ||||||
| chr3:58069058
|
G | A | 17 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(14): Show | 17 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-7988G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069058 | ||||||
| chr3:58069109
|
T | C | 23 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-7937T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069109 | ||||||
| chr3:58069139
|
T | TA | 11 | a0002c0008t0002g0022a0002c0015t0003g0025a0003c0009t0004g0009others(8): Show | 11 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-7892dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58069139 | |||||
| chr3:58069155
|
G | A | 23 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-7891G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069155 | ||||||
| chr3:58069221
|
G | C | 1 | a0001c0053t0001g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.293-7825G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069221 | ||||||
| chr3:58069232
|
C | CT | 17 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0088others(14): Show | 17 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.293-7791dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58069232 | |||||
| chr3:58069232
|
CT | C | 51 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0045others(48): Show | 51 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.293-7791delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58069232 | |||||
| chr3:58069232
|
CTT | C | 5 | a0001c0001t0001g0020a0001c0053t0001g0018a0006c0017t0006g0057others(2): Show | 5 | HG02922.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-7792_293-7791d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58069232 | |||||
| chr3:58069276
|
G | C | 23 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-7770G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069276 | ||||||
| chr3:58069417
|
T | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.293-7629T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069417 | ||||||
| chr3:58069478
|
A | T | 23 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(20): Show | 23 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-7568A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069478 | ||||||
| chr3:58069535
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0053t0001g0018others(4): Show | 7 | HG02922.hp1 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-7511C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069535 | ||||||
| chr3:58069536
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(29): Show | 32 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.293-7510C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069536 | ||||||
| chr3:58069610
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0002g0021others(5): Show | 8 | HG01255.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-7436C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069610 | ||||||
| chr3:58069660
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.293-7386G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069660 | ||||||
| chr3:58069685
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0026t0001g0149 | 3 | HG01516.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.293-7361C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069685 | ||||||
| chr3:58069709
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.293-7337C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069709 | ||||||
| chr3:58069737
|
G | A | 27 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-7309G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58069737 | ||||||
| chr3:58069890
|
C | CA | 27 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-7152dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58069890 | |||||
| chr3:58070039
|
C | CTCTT | 22 | a0001c0001t0001g0014a0001c0001t0003g0089a0001c0014t0001g0111others(19): Show | 22 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.293-6997_293-6994d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070039 | |||||
| chr3:58070049
|
C | CT | 48 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0047others(45): Show | 48 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.293-6980dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070049 | |||||
| chr3:58070049
|
CT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0053t0001g0018others(4): Show | 7 | HG02922.hp1 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-6980delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070049 | |||||
| chr3:58070050
|
T | TTTC | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(33): Show | 36 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.293-6994_293-6993i others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070050 | |||||
| chr3:58070054
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0053t0001g0018others(4): Show | 7 | HG02922.hp1 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-6992T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070054 | ||||||
| chr3:58070132
|
G | A | 1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-6914G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070132 | ||||||
| chr3:58070193
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0047others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-6853G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070193 | ||||||
| chr3:58070310
|
C | G | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.293-6736C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070310 | ||||||
| chr3:58070339
|
C | T | 27 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(24): Show | 27 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-6707C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070339 | ||||||
| chr3:58070407
|
C | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0051others(4): Show | 7 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-6639C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070407 | ||||||
| chr3:58070437
|
A | G | 1 | a0002c0002t0002g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.293-6609A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070437 | ||||||
| chr3:58070465
|
T | C | 16 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(13): Show | 16 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-6581T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070465 | ||||||
| chr3:58070490
|
C | T | 16 | a0001c0001t0001g0014a0001c0014t0001g0111a0001c0014t0001g0115others(13): Show | 16 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-6556C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070490 | ||||||
| chr3:58070644
|
ATCTC | A | 11 | a0001c0014t0001g0111a0001c0014t0001g0115a0002c0004t0001g0156others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-6388_293-6385d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070644 | |||||
| chr3:58070656
|
CTCTCTTT | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(39): Show | 42 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.293-6388_293-6382d others(9): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070656 | |||||
| chr3:58070658
|
CTCT | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0047others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-6386_293-6384d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070658 | |||||
| chr3:58070662
|
T | C | 5 | a0001c0001t0001g0101a0001c0001t0001g0103a0002c0002t0002g0171others(2): Show | 5 | HG00741.hp2 HG02004.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-6384T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070662 | ||||||
| chr3:58070700
|
C | T | 1 | a0002c0007t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.293-6346C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070700 | ||||||
| chr3:58070728
|
T | C | 4 | a0001c0014t0001g0111a0001c0014t0001g0115a0002c0008t0014g0110others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-6318T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070728 | ||||||
| chr3:58070729
|
G | A | 4 | a0001c0014t0001g0111a0001c0014t0001g0115a0002c0008t0014g0110others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-6317G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070729 | ||||||
| chr3:58070779
|
C | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0020others(70): Show | 73 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-6267C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070779 | ||||||
| chr3:58070784
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.293-6262C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070784 | ||||||
| chr3:58070821
|
A | G | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-6225A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070821 | ||||||
| chr3:58070863
|
G | A | 13 | a0001c0001t0001g0151a0002c0004t0001g0156a0002c0008t0002g0155others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-6183G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070863 | ||||||
| chr3:58070891
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0051others(10): Show | 13 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.293-6155C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070891 | ||||||
| chr3:58070898
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.293-6148C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070898 | ||||||
| chr3:58070928
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.293-6118G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58070928 | ||||||
| chr3:58070952
|
G | GT | 18 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0028others(15): Show | 18 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-6081dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58070952 | |||||
| chr3:58071254
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.293-5792A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071254 | ||||||
| chr3:58071260
|
ATC | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0047others(21): Show | 24 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-5781_293-5780d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58071260 | |||||
| chr3:58071274
|
CT | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0014others(78): Show | 81 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-5750delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58071274 | |||||
| chr3:58071274
|
CTT | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(44): Show | 47 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.293-5751_293-5750d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58071274 | |||||
| chr3:58071274
|
CTTT | C | 6 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0041t0001g0016others(3): Show | 6 | HG02818.hp2 HG02970.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-5752_293-5750d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58071274 | |||||
| chr3:58071478
|
C | T | 2 | a0002c0015t0003g0025a0017c0046t0003g0015 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-5568C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071478 | ||||||
| chr3:58071522
|
T | C | 2 | a0002c0015t0003g0025a0017c0046t0003g0015 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-5524T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071522 | ||||||
| chr3:58071607
|
G | C | 3 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0043t0002g0049 | 3 | HG02818.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.293-5439G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071607 | ||||||
| chr3:58071855
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0053t0001g0018others(2): Show | 5 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-5191G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071855 | ||||||
| chr3:58071907
|
C | T | 2 | a0002c0015t0003g0025a0017c0046t0003g0015 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-5139C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071907 | ||||||
| chr3:58071957
|
G | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.293-5089G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58071957 | ||||||
| chr3:58072003
|
AG | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.293-5041delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58072003 | |||||
| chr3:58072103
|
C | T | 24 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(21): Show | 24 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-4943C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072103 | ||||||
| chr3:58072643
|
G | A | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.293-4403G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072643 | ||||||
| chr3:58072760
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.293-4286C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072760 | ||||||
| chr3:58072786
|
T | C | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-4260T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072786 | ||||||
| chr3:58072883
|
G | A | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.293-4163G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072883 | ||||||
| chr3:58072908
|
G | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-4138G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58072908 | ||||||
| chr3:58073012
|
A | T | 1 | a0001c0031t0005g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-4034A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58073012 | ||||||
| chr3:58073149
|
C | CTATTTAT others(1): Show |
68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.293-3874_293-3867d others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073149 | |||||
| chr3:58073149
|
C | CTATTTAT others(5): Show |
24 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0054others(21): Show | 24 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-3878_293-3867d others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073149 | |||||
| chr3:58073149
|
C | CTATTTAT others(9): Show |
16 | a0001c0001t0001g0105a0002c0002t0002g0084a0002c0002t0002g0148others(13): Show | 16 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-3882_293-3867d others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073149 | |||||
| chr3:58073149
|
CTATTTAT others(5): Show |
C | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-3878_293-3867d others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073149 | |||||
| chr3:58073176
|
T | TTTATTTA others(9): Show |
2 | a0002c0002t0002g0070a0002c0002t0002g0125 | 2 | HG00738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.293-3867_293-3866i others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073176 | |||||
| chr3:58073486
|
G | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-3560G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58073486 | ||||||
| chr3:58073511
|
C | T | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-3535C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58073511 | ||||||
| chr3:58073574
|
ATT | A | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.293-3457_293-3456d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58073574 | |||||
| chr3:58073934
|
G | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.293-3112G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58073934 | ||||||
| chr3:58073995
|
T | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.293-3051T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58073995 | ||||||
| chr3:58074001
|
G | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-3045G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074001 | ||||||
| chr3:58074061
|
A | C | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-2985A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074061 | ||||||
| chr3:58074068
|
A | G | 9 | a0002c0004t0001g0156a0002c0008t0002g0022a0002c0008t0002g0155others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-2978A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074068 | ||||||
| chr3:58074421
|
A | G | 2 | a0003c0054t0013g0108a0004c0006t0012g0109 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.293-2625A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074421 | ||||||
| chr3:58074534
|
C | T | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-2512C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074534 | ||||||
| chr3:58074626
|
C | T | 2 | a0003c0054t0013g0108a0004c0006t0012g0109 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.293-2420C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074626 | ||||||
| chr3:58074657
|
C | T | 4 | a0001c0001t0001g0020a0001c0053t0001g0018a0006c0017t0006g0057others(1): Show | 4 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2389C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58074657 | ||||||
| chr3:58075256
|
T | C | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-1790T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075256 | ||||||
| chr3:58075294
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.293-1752A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075294 | ||||||
| chr3:58075332
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.293-1714C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075332 | ||||||
| chr3:58075389
|
T | C | 2 | a0003c0054t0013g0108a0004c0006t0012g0109 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.293-1657T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075389 | ||||||
| chr3:58075535
|
T | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.293-1511T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075535 | ||||||
| chr3:58075577
|
T | C | 43 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.293-1469T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075577 | ||||||
| chr3:58075804
|
A | T | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-1242A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075804 | ||||||
| chr3:58075881
|
G | A | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-1165G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58075881 | ||||||
| chr3:58076024
|
A | G | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-1022A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076024 | ||||||
| chr3:58076165
|
G | T | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.293-881G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076165 | ||||||
| chr3:58076327
|
T | TGCATGTA others(11): Show |
1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-718_293-701dup others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | INFO_REALIGN_3_PRIME | chr3 | 58076327 | |||||
| chr3:58076358
|
G | A | 1 | a0002c0015t0001g0131 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.293-688G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076358 | ||||||
| chr3:58076465
|
C | G | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.293-581C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076465 | ||||||
| chr3:58076535
|
A | G | 1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-511A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076535 | ||||||
| chr3:58076557
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.293-489C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076557 | ||||||
| chr3:58076655
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.293-391T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076655 | ||||||
| chr3:58076698
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.293-348A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076698 | ||||||
| chr3:58076783
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.293-263G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076783 | ||||||
| chr3:58076851
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.293-195G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076851 | ||||||
| chr3:58076884
|
C | A | 7 | a0001c0001t0001g0090a0002c0004t0002g0069a0002c0004t0002g0072others(4): Show | 7 | HG01257.hp1 HG01358.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-162C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076884 | ||||||
| chr3:58076987
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0092a0001c0001t0001g0094others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-59A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58076987 | ||||||
| chr3:58077029
|
T | G | 1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-17T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58077029 | ||||||
| chr3:58077032
|
G | A | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-14G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 1/45 | chr3 | 58077032 | ||||||
| chr3:58077576
|
G | C | 32 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(29): Show | 32 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.541+282G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077576 | ||||||
| chr3:58077582
|
G | C | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.541+288G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077582 | ||||||
| chr3:58077604
|
C | T | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+310C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077604 | ||||||
| chr3:58077678
|
G | A | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+384G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077678 | ||||||
| chr3:58077689
|
T | C | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.541+395T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077689 | ||||||
| chr3:58077906
|
G | T | 30 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(27): Show | 30 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+612G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077906 | ||||||
| chr3:58077961
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.541+667A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58077961 | ||||||
| chr3:58078092
|
G | A | 29 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.542-625G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58078092 | ||||||
| chr3:58078234
|
C | T | 2 | a0001c0014t0001g0111a0001c0014t0001g0115 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.542-483C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 2/45 | chr3 | 58078234 | ||||||
| chr3:58078862
|
C | T | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.639+48C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58078862 | ||||||
| chr3:58078968
|
A | T | 4 | a0002c0015t0003g0025a0010c0057t0001g0046a0011c0056t0001g0112others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+154A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58078968 | ||||||
| chr3:58079255
|
A | AT | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.639+456dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | INFO_REALIGN_3_PRIME | chr3 | 58079255 | |||||
| chr3:58079294
|
C | G | 1 | a0003c0005t0001g0077 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.639+480C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58079294 | ||||||
| chr3:58079844
|
T | C | 4 | a0001c0001t0001g0020a0001c0053t0001g0018a0006c0017t0006g0057others(1): Show | 4 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+1030T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58079844 | ||||||
| chr3:58079924
|
G | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.639+1110G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58079924 | ||||||
| chr3:58079964
|
A | G | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.639+1150A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58079964 | ||||||
| chr3:58079988
|
C | T | 7 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(4): Show | 7 | HG00438.hp2 HG01891.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+1174C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58079988 | ||||||
| chr3:58080131
|
A | C | 9 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(6): Show | 9 | HG00438.hp2 HG01891.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.639+1317A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58080131 | ||||||
| chr3:58080494
|
A | AT | 68 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.640-1117dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | INFO_REALIGN_3_PRIME | chr3 | 58080494 | |||||
| chr3:58080620
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 41 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.640-1009G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58080620 | ||||||
| chr3:58080734
|
C | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0087a0025c0029t0001g0008 | 3 | HG02040.hp2 NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.640-895C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58080734 | ||||||
| chr3:58080791
|
C | CT | 8 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0101others(5): Show | 8 | HG02280.hp2 HG02615.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.640-824dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | INFO_REALIGN_3_PRIME | chr3 | 58080791 | |||||
| chr3:58080791
|
C | CTT | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 42 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.640-825_640-824dup others(2): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | INFO_REALIGN_3_PRIME | chr3 | 58080791 | |||||
| chr3:58080814
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0059others(3): Show | 6 | HG01109.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-815A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58080814 | ||||||
| chr3:58080827
|
T | C | 8 | a0002c0008t0002g0022a0002c0008t0002g0155a0003c0005t0001g0029others(5): Show | 8 | HG00438.hp2 HG02572.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-802T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58080827 | ||||||
| chr3:58081028
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 52 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.640-601A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58081028 | ||||||
| chr3:58081075
|
A | G | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.640-554A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58081075 | ||||||
| chr3:58081149
|
ATG | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0059others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.640-478_640-477del others(2): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | INFO_REALIGN_3_PRIME | chr3 | 58081149 | |||||
| chr3:58081188
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0051a0002c0015t0003g0025others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-441G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 3/45 | chr3 | 58081188 | ||||||
| chr3:58081802
|
A | G | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.787+26A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58081802 | ||||||
| chr3:58082011
|
TTAGTGC | T | 4 | a0002c0003t0002g0138a0002c0003t0002g0139a0002c0003t0002g0140others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.787+236_787+241del others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082011 | ||||||
| chr3:58082020
|
TA | T | 4 | a0002c0003t0002g0138a0002c0003t0002g0139a0002c0003t0002g0140others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.787+245delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082020 | ||||||
| chr3:58082068
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.787+292C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082068 | ||||||
| chr3:58082243
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(4): Show | 7 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.787+467G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082243 | ||||||
| chr3:58082273
|
A | G | 12 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(9): Show | 12 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.787+497A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082273 | ||||||
| chr3:58082519
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.787+743T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082519 | ||||||
| chr3:58082541
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.787+765C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082541 | ||||||
| chr3:58082769
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.787+993C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082769 | ||||||
| chr3:58082774
|
CA | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.787+1010delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58082774 | |||||
| chr3:58082787
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+1011C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58082787 | ||||||
| chr3:58083239
|
CT | C | 69 | a0001c0001t0001g0045a0001c0001t0001g0087a0001c0014t0001g0111others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.787+1481delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58083239 | |||||
| chr3:58083257
|
T | A | 1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.787+1481T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083257 | ||||||
| chr3:58083288
|
G | A | 1 | a0001c0053t0001g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.787+1512G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083288 | ||||||
| chr3:58083367
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0003g0089others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+1612dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58083367 | |||||
| chr3:58083367
|
CT | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0054others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.787+1612delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58083367 | |||||
| chr3:58083510
|
G | GCATC | 10 | a0002c0002t0002g0120a0005c0010t0002g0065a0005c0010t0003g0002others(7): Show | 10 | HG02451.hp2 HG02559.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.787+1737_787+1740d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58083510 | |||||
| chr3:58083516
|
A | G | 3 | a0003c0054t0013g0108a0004c0006t0012g0109a0020c0052t0001g0117 | 3 | HG02630.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.787+1740A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083516 | ||||||
| chr3:58083586
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+1810C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083586 | ||||||
| chr3:58083619
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0040 | 2 | HG03927.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.787+1843G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083619 | ||||||
| chr3:58083652
|
A | G | 3 | a0003c0054t0013g0108a0004c0006t0012g0109a0020c0052t0001g0117 | 3 | HG02630.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.787+1876A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083652 | ||||||
| chr3:58083700
|
C | T | 10 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(7): Show | 10 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.787+1924C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083700 | ||||||
| chr3:58083702
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.787+1926A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083702 | ||||||
| chr3:58083916
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.787+2140C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083916 | ||||||
| chr3:58083917
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.787+2141G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083917 | ||||||
| chr3:58083970
|
G | A | 1 | a0002c0003t0001g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.787+2194G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58083970 | ||||||
| chr3:58084013
|
G | A | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.787+2237G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084013 | ||||||
| chr3:58084053
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+2277G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084053 | ||||||
| chr3:58084062
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.787+2286C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084062 | ||||||
| chr3:58084073
|
T | A | 2 | a0002c0012t0002g0118a0002c0012t0002g0152 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.787+2297T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084073 | ||||||
| chr3:58084147
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+2371G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084147 | ||||||
| chr3:58084191
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.787+2424_787+2433d others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58084191 | |||||
| chr3:58084191
|
CA | C | 5 | a0001c0001t0001g0086a0002c0002t0002g0006a0002c0002t0002g0162others(2): Show | 5 | HG02300.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.787+2433delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58084191 | |||||
| chr3:58084276
|
C | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+2500C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084276 | ||||||
| chr3:58084366
|
G | GT | 2 | a0001c0001t0001g0053a0001c0001t0001g0056 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.787+2591dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58084366 | |||||
| chr3:58084532
|
C | T | 3 | a0007c0016t0004g0095a0007c0016t0004g0096a0021c0047t0004g0093 | 3 | HG02451.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.787+2756C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084532 | ||||||
| chr3:58084555
|
T | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.787+2779T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084555 | ||||||
| chr3:58084555
|
T | TTA | 4 | a0001c0001t0001g0020a0001c0001t0001g0051a0013c0022t0001g0116others(1): Show | 4 | HG02922.hp2 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.787+2779_787+2780i others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084555 | ||||||
| chr3:58084555
|
TA | T | 5 | a0002c0002t0002g0126a0002c0003t0002g0138a0002c0003t0002g0139others(2): Show | 5 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.787+2788delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58084555 | |||||
| chr3:58084556
|
A | T | 1 | a0002c0003t0007g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.787+2780A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084556 | ||||||
| chr3:58084564
|
A | AT | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.787+2797dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58084564 | |||||
| chr3:58084564
|
A | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0063others(5): Show | 8 | HG02293.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+2788A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084564 | ||||||
| chr3:58084578
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+2802G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084578 | ||||||
| chr3:58084620
|
A | G | 13 | a0001c0001t0001g0045a0002c0002t0002g0126a0002c0003t0001g0134others(10): Show | 13 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.787+2844A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084620 | ||||||
| chr3:58084687
|
G | A | 1 | a0002c0004t0002g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.787+2911G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084687 | ||||||
| chr3:58084773
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+2997T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084773 | ||||||
| chr3:58084803
|
C | A | 25 | a0001c0001t0001g0045a0002c0002t0002g0120a0002c0002t0002g0126others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.787+3027C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084803 | ||||||
| chr3:58084973
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+3197T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58084973 | ||||||
| chr3:58085158
|
T | A | 1 | a0001c0001t0003g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.787+3382T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085158 | ||||||
| chr3:58085215
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.787+3439A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085215 | ||||||
| chr3:58085281
|
G | GA | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.787+3506dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58085281 | |||||
| chr3:58085444
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+3668G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085444 | ||||||
| chr3:58085456
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.787+3680A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085456 | ||||||
| chr3:58085679
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+3903G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085679 | ||||||
| chr3:58085815
|
C | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.787+4039C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085815 | ||||||
| chr3:58085874
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.787+4098G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085874 | ||||||
| chr3:58085917
|
C | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.787+4141C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58085917 | ||||||
| chr3:58086086
|
T | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0051a0003c0054t0013g0108others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.787+4310T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086086 | ||||||
| chr3:58086126
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.787+4350G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086126 | ||||||
| chr3:58086130
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.787+4354G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086130 | ||||||
| chr3:58086132
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.787+4356A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086132 | ||||||
| chr3:58086159
|
CT | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.787+4396delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58086159 | |||||
| chr3:58086255
|
C | T | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.787+4479C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086255 | ||||||
| chr3:58086370
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.787+4594C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086370 | ||||||
| chr3:58086462
|
CT | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.787+4692delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58086462 | |||||
| chr3:58086610
|
C | G | 2 | a0003c0054t0013g0108a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.787+4834C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086610 | ||||||
| chr3:58086724
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.787+4948G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086724 | ||||||
| chr3:58086744
|
T | G | 19 | a0001c0001t0001g0020a0001c0001t0001g0051a0002c0004t0001g0156others(16): Show | 19 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.787+4968T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58086744 | ||||||
| chr3:58087108
|
TCAAA | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.787+5349_787+5352d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58087108 | |||||
| chr3:58087251
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.787+5475C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087251 | ||||||
| chr3:58087252
|
G | A | 1 | a0002c0020t0003g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.787+5476G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087252 | ||||||
| chr3:58087454
|
T | G | 2 | a0003c0054t0013g0108a0020c0052t0001g0117 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.787+5678T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087454 | ||||||
| chr3:58087694
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.787+5918C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087694 | ||||||
| chr3:58087741
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.787+5965C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087741 | ||||||
| chr3:58087744
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787+5968C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087744 | ||||||
| chr3:58087747
|
G | C | 10 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(7): Show | 10 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.787+5971G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087747 | ||||||
| chr3:58087810
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787+6034G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087810 | ||||||
| chr3:58087821
|
A | G | 1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.787+6045A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087821 | ||||||
| chr3:58087834
|
G | A | 1 | a0027c0039t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.787+6058G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087834 | ||||||
| chr3:58087936
|
C | T | 12 | a0002c0002t0002g0120a0005c0010t0002g0013a0005c0010t0002g0065others(9): Show | 12 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.787+6160C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087936 | ||||||
| chr3:58087961
|
A | T | 1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.787+6185A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58087961 | ||||||
| chr3:58088015
|
A | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787+6239A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088015 | ||||||
| chr3:58088031
|
G | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.787+6255G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088031 | ||||||
| chr3:58088038
|
C | CT | 14 | a0002c0002t0002g0126a0002c0002t0002g0162a0002c0003t0001g0134others(11): Show | 14 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.787+6284dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58088038 | |||||
| chr3:58088038
|
C | CTT | 5 | a0002c0003t0002g0052a0002c0003t0002g0139a0002c0003t0002g0141others(2): Show | 5 | HG01106.hp2 HG01361.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.787+6283_787+6284d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58088038 | |||||
| chr3:58088038
|
CT | C | 8 | a0001c0001t0001g0059a0001c0001t0001g0088a0002c0008t0002g0022others(5): Show | 8 | HG01169.hp1 HG01192.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+6284delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58088038 | |||||
| chr3:58088038
|
CTT | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.787+6283_787+6284d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58088038 | |||||
| chr3:58088121
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.787+6345A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088121 | ||||||
| chr3:58088193
|
A | G | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787+6417A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088193 | ||||||
| chr3:58088325
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.788-6511G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088325 | ||||||
| chr3:58088380
|
T | A | 1 | a0002c0018t0002g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.788-6456T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58088380 | ||||||
| chr3:58088505
|
AG | A | 5 | a0002c0002t0001g0176a0002c0018t0002g0136a0002c0018t0002g0173others(2): Show | 5 | HG00741.hp1 HG01106.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-6329delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58088505 | |||||
| chr3:58089119
|
G | A | 45 | a0001c0001t0001g0059a0002c0002t0002g0120a0002c0002t0002g0126others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.788-5717G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089119 | ||||||
| chr3:58089196
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.788-5640T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089196 | ||||||
| chr3:58089435
|
A | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.788-5401A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089435 | ||||||
| chr3:58089546
|
C | CA | 15 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(12): Show | 15 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.788-5275dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58089546 | |||||
| chr3:58089546
|
C | CAA | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.788-5276_788-5275d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58089546 | |||||
| chr3:58089632
|
A | G | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.788-5204A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089632 | ||||||
| chr3:58089667
|
T | C | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-5169T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089667 | ||||||
| chr3:58089737
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-5099G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089737 | ||||||
| chr3:58089778
|
T | C | 8 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0034others(5): Show | 8 | HG02602.hp1 HG03017.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.788-5058T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089778 | ||||||
| chr3:58089975
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.788-4861C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58089975 | ||||||
| chr3:58090035
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.788-4801G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090035 | ||||||
| chr3:58090058
|
A | G | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.788-4778A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090058 | ||||||
| chr3:58090139
|
C | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-4697C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090139 | ||||||
| chr3:58090148
|
CT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.788-4674delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58090148 | |||||
| chr3:58090179
|
C | G | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-4657C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090179 | ||||||
| chr3:58090229
|
A | C | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-4607A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090229 | ||||||
| chr3:58090412
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-4424G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090412 | ||||||
| chr3:58090472
|
A | G | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.788-4364A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090472 | ||||||
| chr3:58090474
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0101 | 2 | NA18979.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.788-4362A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090474 | ||||||
| chr3:58090725
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.788-4111T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090725 | ||||||
| chr3:58090764
|
C | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.788-4072C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090764 | ||||||
| chr3:58090838
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.788-3998G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090838 | ||||||
| chr3:58090908
|
C | G | 4 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-3928C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58090908 | ||||||
| chr3:58091088
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.788-3748A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58091088 | ||||||
| chr3:58091126
|
A | G | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-3710A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58091126 | ||||||
| chr3:58091242
|
C | G | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-3594C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58091242 | ||||||
| chr3:58091276
|
A | G | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788-3560A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58091276 | ||||||
| chr3:58091629
|
T | TA | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.788-3198dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58091629 | |||||
| chr3:58091814
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.788-3022T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58091814 | ||||||
| chr3:58092327
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.788-2509G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092327 | ||||||
| chr3:58092505
|
G | A | 4 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(1): Show | 4 | HG02922.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-2331G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092505 | ||||||
| chr3:58092557
|
G | A | 1 | a0005c0010t0002g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.788-2279G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092557 | ||||||
| chr3:58092593
|
C | T | 1 | a0001c0026t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.788-2243C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092593 | ||||||
| chr3:58092784
|
T | G | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.788-2052T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092784 | ||||||
| chr3:58092834
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.788-2002G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092834 | ||||||
| chr3:58092916
|
A | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-1920A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092916 | ||||||
| chr3:58092990
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.788-1846G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58092990 | ||||||
| chr3:58093047
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.788-1789T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093047 | ||||||
| chr3:58093222
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(3): Show | 6 | HG01891.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.788-1614C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093222 | ||||||
| chr3:58093272
|
A | G | 9 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(6): Show | 9 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-1564A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093272 | ||||||
| chr3:58093462
|
G | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-1374G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093462 | ||||||
| chr3:58093630
|
T | C | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-1206T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093630 | ||||||
| chr3:58093633
|
T | TCA | 12 | a0002c0002t0002g0126a0002c0003t0001g0134a0002c0003t0002g0052others(9): Show | 12 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.788-1177_788-1176d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58093633 | |||||
| chr3:58093633
|
TCA | T | 2 | a0002c0012t0002g0152a0003c0054t0013g0108 | 2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.788-1177_788-1176d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58093633 | |||||
| chr3:58093633
|
TCACA | T | 9 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(6): Show | 9 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-1179_788-1176d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58093633 | |||||
| chr3:58093633
|
TCACACA | T | 3 | a0003c0035t0003g0060a0004c0006t0012g0109a0020c0052t0001g0117 | 3 | HG02630.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.788-1181_788-1176d others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58093633 | |||||
| chr3:58093633
|
TCACACAC others(1): Show |
T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.788-1183_788-1176d others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | INFO_REALIGN_3_PRIME | chr3 | 58093633 | |||||
| chr3:58093699
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.788-1137A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093699 | ||||||
| chr3:58093904
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.788-932C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58093904 | ||||||
| chr3:58094044
|
C | T | 9 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(6): Show | 9 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-792C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094044 | ||||||
| chr3:58094119
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.788-717G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094119 | ||||||
| chr3:58094228
|
T | G | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.788-608T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094228 | ||||||
| chr3:58094673
|
C | T | 11 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(8): Show | 11 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.788-163C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094673 | ||||||
| chr3:58094763
|
A | G | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.788-73A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094763 | ||||||
| chr3:58094778
|
G | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.788-58G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 4/45 | chr3 | 58094778 | ||||||
| chr3:58095007
|
G | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.906+53G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095007 | ||||||
| chr3:58095060
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0098a0001c0001t0002g0099 | 3 | HG02451.hp1 HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.906+106A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095060 | ||||||
| chr3:58095221
|
T | G | 5 | a0002c0002t0001g0176a0002c0018t0002g0136a0002c0018t0002g0173others(2): Show | 5 | HG00741.hp1 HG01106.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+267T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095221 | ||||||
| chr3:58095225
|
G | GTATT | 4 | a0004c0006t0012g0109a0006c0017t0006g0024a0006c0017t0006g0057others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+274_906+275ins others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095225 | |||||
| chr3:58095225
|
G | GTATTTAT others(5): Show |
7 | a0001c0001t0001g0090a0001c0053t0001g0018a0003c0005t0001g0029others(4): Show | 7 | HG00438.hp2 HG01358.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+274_906+275ins others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095225 | |||||
| chr3:58095225
|
G | GTATTTAT others(9): Show |
3 | a0001c0001t0001g0059a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.906+274_906+275ins others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095225 | |||||
| chr3:58095225
|
G | GTATTTAT others(13): Show |
1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.906+274_906+275ins others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095225 | |||||
| chr3:58095229
|
G | GTATGTAT others(5): Show |
11 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(8): Show | 11 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+278_906+279ins others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATGTAT others(9): Show |
4 | a0001c0001t0001g0114a0001c0001t0002g0058a0002c0020t0003g0123others(1): Show | 4 | HG01081.hp2 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+278_906+279ins others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATGTAT others(13): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0051a0011c0056t0001g0112others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+278_906+279ins others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATTTAT others(5): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0146 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.906+292_906+303dup others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATTTAT others(9): Show |
51 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(48): Show | 51 | HG00438.hp1 HG01071.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.906+288_906+303dup others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATTTAT others(13): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0030others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.906+284_906+303dup others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | GTATTTAT others(17): Show |
1 | a0027c0039t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.906+280_906+303dup others(24): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095229 | |||||
| chr3:58095229
|
G | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0090a0001c0053t0001g0018others(16): Show | 19 | HG00438.hp2 HG00741.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+275G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095229 | ||||||
| chr3:58095255
|
A | ATTTATTT others(10): Show |
1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.906+303_906+304ins others(17): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | INFO_REALIGN_3_PRIME | chr3 | 58095255 | |||||
| chr3:58095280
|
G | C | 11 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(8): Show | 11 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+326G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095280 | ||||||
| chr3:58095536
|
G | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.906+582G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095536 | ||||||
| chr3:58095546
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.906+592G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095546 | ||||||
| chr3:58095614
|
C | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.907-527C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095614 | ||||||
| chr3:58095630
|
T | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.907-511T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095630 | ||||||
| chr3:58095679
|
A | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.907-462A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095679 | ||||||
| chr3:58095728
|
T | A | 1 | a0004c0041t0001g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.907-413T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095728 | ||||||
| chr3:58095763
|
C | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.907-378C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095763 | ||||||
| chr3:58095877
|
G | C | 1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-264G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095877 | ||||||
| chr3:58095908
|
A | T | 1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907-233A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58095908 | ||||||
| chr3:58096026
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.907-115C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 5/45 | chr3 | 58096026 | ||||||
| chr3:58096265
|
G | A | 1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.984+47G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096265 | ||||||
| chr3:58096412
|
C | G | 10 | a0001c0001t0001g0059a0001c0026t0001g0149a0002c0008t0002g0022others(7): Show | 10 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.984+194C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096412 | ||||||
| chr3:58096582
|
C | G | 9 | a0001c0001t0001g0059a0002c0008t0002g0022a0002c0008t0002g0155others(6): Show | 9 | HG00438.hp2 HG02735.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.984+364C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096582 | ||||||
| chr3:58096611
|
C | T | 1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.984+393C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096611 | ||||||
| chr3:58096633
|
C | T | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.984+415C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096633 | ||||||
| chr3:58096681
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.984+463G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096681 | ||||||
| chr3:58096734
|
C | A | 1 | a0001c0031t0005g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.984+516C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096734 | ||||||
| chr3:58096982
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.984+764G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58096982 | ||||||
| chr3:58097012
|
AG | A | 11 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(8): Show | 11 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.984+796delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | INFO_REALIGN_3_PRIME | chr3 | 58097012 | |||||
| chr3:58097099
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.985-716C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58097099 | ||||||
| chr3:58097231
|
A | G | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-584A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58097231 | ||||||
| chr3:58097261
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.985-554G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58097261 | ||||||
| chr3:58097299
|
A | G | 1 | a0005c0011t0003g0011 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.985-516A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58097299 | ||||||
| chr3:58097719
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.985-96G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 6/45 | chr3 | 58097719 | ||||||
| chr3:58098321
|
G | C | 1 | a0001c0019t0001g0122 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1147+344G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 7/45 | chr3 | 58098321 | ||||||
| chr3:58098344
|
T | C | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1147+367T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 7/45 | chr3 | 58098344 | ||||||
| chr3:58099068
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1345+160A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58099068 | ||||||
| chr3:58099168
|
A | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1345+260A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58099168 | ||||||
| chr3:58099456
|
C | T | 1 | a0002c0003t0002g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1345+548C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58099456 | ||||||
| chr3:58099542
|
C | CTGTTT | 3 | a0002c0002t0002g0124a0002c0008t0014g0110a0002c0015t0001g0131 | 3 | HG01167.hp1 HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1345+656_1345+660d others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58099542 | |||||
| chr3:58100365
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1345+1457A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100365 | ||||||
| chr3:58100365
|
A | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1345+1457A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100365 | ||||||
| chr3:58100369
|
A | AATATATA others(35): Show |
1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1345+1462_1345+146 others(46): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100369 | |||||
| chr3:58100371
|
A | AATATATA others(19): Show |
1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1345+1464_1345+146 others(30): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100371 | |||||
| chr3:58100371
|
A | ATATATAT others(6): Show |
1 | a0002c0015t0003g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1345+1463_1345+146 others(17): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100371 | ||||||
| chr3:58100371
|
A | T | 1 | a0004c0006t0012g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1345+1463A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100371 | ||||||
| chr3:58100373
|
A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0062others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(21): Show |
1 | a0005c0048t0005g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(32): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0042a0002c0020t0003g0123 | 2 | HG01891.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(25): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(22): Show |
1 | a0005c0011t0003g0011 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(33): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(24): Show |
6 | a0005c0010t0002g0065a0005c0010t0003g0002a0005c0011t0004g0142others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(35): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(15): Show |
20 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0033others(17): Show | 20 | HG00438.hp1 HG01169.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0132a0005c0037t0003g0129 | 2 | HG01071.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(28): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(19): Show |
1 | a0003c0005t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(30): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAA others(23): Show |
2 | a0002c0007t0002g0174a0005c0011t0003g0119 | 2 | HG03704.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(34): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(14): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0085a0001c0001t0001g0091others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(25): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(16): Show |
2 | a0001c0001t0001g0061a0003c0005t0001g0044 | 2 | NA18957.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(27): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(18): Show |
2 | a0001c0001t0001g0076a0002c0036t0009g0075 | 2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(29): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(24): Show |
1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(35): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(26): Show |
1 | a0002c0002t0002g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(37): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAAAT others(28): Show |
1 | a0002c0004t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(39): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAATA others(15): Show |
28 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0036others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAATA others(17): Show |
12 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0038others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(28): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAATA others(19): Show |
12 | a0002c0004t0002g0069a0002c0004t0002g0072a0002c0004t0002g0074others(9): Show | 12 | HG00280.hp2 HG00438.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(30): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAATA others(29): Show |
1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(40): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAAATA others(39): Show |
1 | a0003c0009t0004g0026 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(50): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(17): Show |
1 | a0025c0029t0001g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(28): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(14): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0040a0004c0006t0002g0050 | 3 | HG03927.hp2 NA18957.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(25): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(16): Show |
1 | a0001c0001t0001g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(27): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(18): Show |
1 | a0001c0001t0001g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(29): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(24): Show |
1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(35): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(32): Show |
1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(43): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAAATAT others(46): Show |
1 | a0003c0009t0004g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(57): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAATATA others(15): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0034others(4): Show | 7 | HG01109.hp2 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAATATA others(17): Show |
2 | a0002c0012t0002g0118a0003c0005t0001g0100 | 2 | HG03209.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(28): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAATATA others(19): Show |
1 | a0003c0005t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(30): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAAATATA others(21): Show |
1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(32): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(20): Show |
2 | a0002c0008t0002g0155a0002c0008t0014g0110 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(31): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(22): Show |
2 | a0005c0010t0002g0013a0010c0057t0001g0046 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1345+1466_1345+146 others(33): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(24): Show |
1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(35): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(26): Show |
1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(37): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(36): Show |
1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(47): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AAATATAT others(38): Show |
1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1345+1466_1345+146 others(49): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345+1477_1345+147 others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AATATATA others(17): Show |
7 | a0002c0003t0002g0052a0002c0003t0002g0138a0002c0003t0002g0139others(4): Show | 7 | HG01106.hp2 HG01361.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345+1477_1345+147 others(28): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AATATATA others(19): Show |
5 | a0002c0003t0001g0134a0002c0003t0002g0133a0002c0003t0007g0127others(2): Show | 5 | HG00099.hp1 HG01081.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+1477_1345+147 others(30): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AATATATA others(21): Show |
1 | a0002c0003t0002g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1345+1477_1345+147 others(32): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | AATATATA others(37): Show |
1 | a0003c0009t0004g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+1477_1345+147 others(48): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100373 | |||||
| chr3:58100373
|
A | ATATATAT others(22): Show |
1 | a0004c0021t0001g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1345+1465_1345+146 others(33): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100373 | ||||||
| chr3:58100373
|
A | T | 7 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0147others(4): Show | 7 | HG00280.hp1 HG01109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345+1465A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100373 | ||||||
| chr3:58100475
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1345+1567G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100475 | ||||||
| chr3:58100589
|
C | CT | 32 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0028others(29): Show | 32 | HG00408.hp1 HG00408.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1346-1603dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100589 | |||||
| chr3:58100596
|
T | G | 1 | a0002c0002t0002g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1346-1607T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100596 | ||||||
| chr3:58100599
|
TTG | T | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-1602_1346-160 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | INFO_REALIGN_3_PRIME | chr3 | 58100599 | |||||
| chr3:58100601
|
G | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1346-1602G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100601 | ||||||
| chr3:58100606
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1346-1597G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100606 | ||||||
| chr3:58100688
|
C | A | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-1515C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58100688 | ||||||
| chr3:58101271
|
T | C | 42 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(39): Show | 42 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1346-932T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101271 | ||||||
| chr3:58101353
|
C | T | 1 | a0018c0050t0002g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1346-850C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101353 | ||||||
| chr3:58101391
|
G | A | 1 | a0005c0037t0003g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1346-812G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101391 | ||||||
| chr3:58101492
|
G | A | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-711G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101492 | ||||||
| chr3:58101504
|
C | T | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346-699C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101504 | ||||||
| chr3:58101505
|
G | A | 18 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(15): Show | 18 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1346-698G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 8/45 | chr3 | 58101505 | ||||||
| chr3:58102375
|
G | A | 1 | a0019c0045t0002g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1483+35G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58102375 | ||||||
| chr3:58102471
|
C | G | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483+131C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58102471 | ||||||
| chr3:58102677
|
C | G | 1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1483+337C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58102677 | ||||||
| chr3:58102697
|
T | C | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483+357T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58102697 | ||||||
| chr3:58103110
|
C | T | 18 | a0002c0004t0001g0156a0002c0004t0002g0069a0002c0004t0002g0072others(15): Show | 18 | HG00280.hp2 HG01257.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.1483+770C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103110 | ||||||
| chr3:58103140
|
A | T | 1 | a0005c0010t0002g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1483+800A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103140 | ||||||
| chr3:58103212
|
A | G | 24 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(21): Show | 24 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1484-747A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103212 | ||||||
| chr3:58103265
|
G | GGT | 38 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(35): Show | 38 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1484-666_1484-665d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
G | GGTGT | 3 | a0005c0010t0002g0013a0015c0024t0002g0012a0020c0052t0001g0117 | 3 | HG02559.hp2 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1484-668_1484-665d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
G | GGTGTGT | 11 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(8): Show | 11 | HG00438.hp2 HG01891.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1484-670_1484-665d others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
G | GGTGTGTG others(7): Show |
1 | a0002c0004t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1484-678_1484-665d others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
G | GGTGTGTG others(9): Show |
5 | a0002c0004t0002g0170a0002c0007t0002g0164a0002c0007t0002g0174others(2): Show | 5 | HG00280.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-680_1484-665d others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
G | GGTGTGTG others(11): Show |
5 | a0002c0004t0002g0069a0002c0004t0002g0072a0002c0004t0002g0074others(2): Show | 5 | HG01257.hp1 HG01361.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-682_1484-665d others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103265
|
GGT | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 84 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1484-666_1484-665d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103265 | |||||
| chr3:58103328
|
A | G | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-631A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103328 | ||||||
| chr3:58103440
|
T | G | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-519T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103440 | ||||||
| chr3:58103764
|
A | C | 5 | a0003c0005t0001g0029a0003c0005t0001g0077a0003c0005t0001g0080others(2): Show | 5 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-195A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103764 | ||||||
| chr3:58103789
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1484-170A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103789 | ||||||
| chr3:58103851
|
G | A | 1 | a0002c0003t0002g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1484-108G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103851 | ||||||
| chr3:58103858
|
T | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1484-101T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | chr3 | 58103858 | ||||||
| chr3:58103867
|
GT | G | 66 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(63): Show | 66 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1484-90delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 9/45 | INFO_REALIGN_3_PRIME | chr3 | 58103867 | |||||
| chr3:58104124
|
G | A | 12 | a0002c0002t0002g0126a0002c0003t0001g0134a0002c0003t0002g0052others(9): Show | 12 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1610+39G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | chr3 | 58104124 | ||||||
| chr3:58104150
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1610+65A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | chr3 | 58104150 | ||||||
| chr3:58104198
|
C | CT | 9 | a0001c0001t0001g0003a0002c0018t0002g0136a0003c0005t0001g0029others(6): Show | 9 | HG00438.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1610+130dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr3 | 58104198 | |||||
| chr3:58104198
|
CT | C | 25 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1610+130delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | INFO_REALIGN_3_PRIME | chr3 | 58104198 | |||||
| chr3:58104331
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1610+246G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | chr3 | 58104331 | ||||||
| chr3:58104909
|
A | G | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1611-171A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | chr3 | 58104909 | ||||||
| chr3:58105008
|
A | G | 6 | a0002c0004t0002g0069a0002c0004t0002g0072a0002c0004t0002g0074others(3): Show | 6 | HG01257.hp1 HG01361.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611-72A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 10/45 | chr3 | 58105008 | ||||||
| chr3:58105359
|
C | T | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1747+143C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105359 | ||||||
| chr3:58105371
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 84 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1747+155C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105371 | ||||||
| chr3:58105400
|
G | C | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+184G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105400 | ||||||
| chr3:58105440
|
G | A | 1 | a0002c0004t0002g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1747+224G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105440 | ||||||
| chr3:58105468
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1747+252G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105468 | ||||||
| chr3:58105834
|
G | A | 5 | a0002c0002t0002g0126a0002c0003t0002g0138a0002c0003t0002g0139others(2): Show | 5 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1747+618G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58105834 | ||||||
| chr3:58106038
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1748-642A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106038 | ||||||
| chr3:58106134
|
G | C | 47 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(44): Show | 47 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1748-546G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106134 | ||||||
| chr3:58106283
|
C | T | 2 | a0003c0035t0003g0060a0003c0054t0013g0108 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1748-397C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106283 | ||||||
| chr3:58106352
|
C | CTA | 21 | a0002c0002t0002g0070a0002c0002t0002g0165a0002c0002t0002g0166others(18): Show | 21 | HG00738.hp1 HG00741.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1748-304_1748-303d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATA | 2 | a0004c0006t0002g0050a0020c0052t0001g0117 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1748-306_1748-303d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATA | 3 | a0002c0015t0003g0025a0002c0051t0008g0153a0018c0050t0002g0082 | 3 | HG01109.hp1 HG03834.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1748-308_1748-303d others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(1): Show |
3 | a0002c0002t0001g0176a0002c0018t0002g0136a0002c0018t0002g0173 | 3 | HG00741.hp1 HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1748-310_1748-303d others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(3): Show |
1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1748-312_1748-303d others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(7): Show |
1 | a0015c0024t0002g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1748-316_1748-303d others(16): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(9): Show |
3 | a0002c0004t0002g0069a0002c0004t0002g0074a0002c0004t0002g0106 | 3 | HG01361.hp2 HG01975.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1748-318_1748-303d others(18): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(11): Show |
3 | a0002c0002t0002g0147a0002c0004t0002g0170a0004c0006t0012g0109 | 3 | HG06807.hp2 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1748-320_1748-303d others(20): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(13): Show |
4 | a0002c0002t0002g0125a0002c0004t0002g0072a0002c0004t0002g0130others(1): Show | 4 | HG01257.hp1 HG01261.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-322_1748-303d others(22): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(15): Show |
4 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0177others(1): Show | 4 | HG00280.hp2 HG01358.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-324_1748-303d others(24): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
C | CTATATAT others(17): Show |
2 | a0002c0002t0002g0150a0002c0004t0001g0156 | 2 | HG00280.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1748-326_1748-303d others(26): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
CTA | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(17): Show | 20 | HG00408.hp2 HG01081.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1748-304_1748-303d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
CTATA | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1748-306_1748-303d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
CTATATA | C | 8 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(5): Show | 8 | HG00438.hp2 HG02735.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-308_1748-303d others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106352
|
CTATATAT others(5): Show |
C | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1748-314_1748-303d others(14): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | INFO_REALIGN_3_PRIME | chr3 | 58106352 | |||||
| chr3:58106470
|
G | T | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1748-210G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106470 | ||||||
| chr3:58106477
|
A | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1748-203A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106477 | ||||||
| chr3:58106479
|
A | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1748-201A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106479 | ||||||
| chr3:58106481
|
A | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1748-199A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106481 | ||||||
| chr3:58106607
|
A | G | 1 | a0002c0002t0002g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1748-73A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106607 | ||||||
| chr3:58106619
|
A | G | 42 | a0002c0002t0002g0120a0002c0002t0002g0126a0002c0003t0001g0134others(39): Show | 42 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1748-61A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 11/45 | chr3 | 58106619 | ||||||
| chr3:58107011
|
A | ATTTG | 2 | a0001c0001t0001g0178a0002c0002t0002g0070 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1941+170_1941+173d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr3 | 58107011 | |||||
| chr3:58107011
|
ATTTG | A | 2 | a0001c0001t0001g0088a0005c0037t0003g0129 | 2 | HG01192.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1941+170_1941+173d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr3 | 58107011 | |||||
| chr3:58107011
|
ATTTGTTT others(1): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0056 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1941+166_1941+173d others(10): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr3 | 58107011 | |||||
| chr3:58107175
|
A | G | 1 | a0002c0002t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1941+302A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107175 | ||||||
| chr3:58107190
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 139 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1941+317T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107190 | ||||||
| chr3:58107191
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1941+318G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107191 | ||||||
| chr3:58107203
|
T | C | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1941+330T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107203 | ||||||
| chr3:58107406
|
T | C | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1941+533T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107406 | ||||||
| chr3:58107561
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0098a0001c0001t0002g0099others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1941+688G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107561 | ||||||
| chr3:58107629
|
A | AT | 8 | a0001c0001t0001g0083a0003c0005t0001g0029a0003c0005t0001g0043others(5): Show | 8 | HG00408.hp1 HG00438.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1941+765dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr3 | 58107629 | |||||
| chr3:58107647
|
C | T | 1 | a0005c0037t0003g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1941+774C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107647 | ||||||
| chr3:58107845
|
A | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1942-613A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107845 | ||||||
| chr3:58107878
|
G | A | 8 | a0001c0001t0001g0083a0003c0005t0001g0029a0003c0005t0001g0043others(5): Show | 8 | HG00408.hp1 HG00438.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1942-580G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58107878 | ||||||
| chr3:58108020
|
C | G | 1 | a0009c0028t0002g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1942-438C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108020 | ||||||
| chr3:58108044
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1942-414C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108044 | ||||||
| chr3:58108067
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-391A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108067 | ||||||
| chr3:58108075
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-383C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108075 | ||||||
| chr3:58108076
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-382T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108076 | ||||||
| chr3:58108077
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-381T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108077 | ||||||
| chr3:58108078
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-380G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108078 | ||||||
| chr3:58108079
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-379G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108079 | ||||||
| chr3:58108080
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1942-378G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108080 | ||||||
| chr3:58108087
|
A | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0076 | 3 | HG02004.hp1 HG02040.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1942-371A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108087 | ||||||
| chr3:58108122
|
A | C | 5 | a0002c0002t0002g0070a0002c0002t0002g0165a0002c0002t0002g0166others(2): Show | 5 | HG00738.hp1 HG00741.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1942-336A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108122 | ||||||
| chr3:58108125
|
C | CA | 8 | a0001c0001t0001g0083a0003c0005t0001g0029a0003c0005t0001g0043others(5): Show | 8 | HG00408.hp1 HG00438.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1942-323dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | INFO_REALIGN_3_PRIME | chr3 | 58108125 | |||||
| chr3:58108209
|
C | T | 1 | a0006c0017t0006g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1942-249C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108209 | ||||||
| chr3:58108215
|
C | T | 5 | a0002c0015t0003g0025a0003c0009t0004g0009a0003c0009t0004g0017others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942-243C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108215 | ||||||
| chr3:58108430
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1942-28A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 12/45 | chr3 | 58108430 | ||||||
| chr3:58108669
|
C | T | 1 | a0002c0002t0002g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2055+98C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 13/45 | chr3 | 58108669 | ||||||
| chr3:58108792
|
G | A | 15 | a0002c0015t0003g0025a0002c0018t0002g0136a0002c0018t0002g0173others(12): Show | 15 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2055+221G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 13/45 | chr3 | 58108792 | ||||||
| chr3:58108823
|
G | A | 4 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(1): Show | 4 | HG01255.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+252G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 13/45 | chr3 | 58108823 | ||||||
| chr3:58108833
|
G | A | 2 | a0002c0012t0002g0118a0002c0012t0002g0152 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2055+262G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 13/45 | chr3 | 58108833 | ||||||
| chr3:58109125
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2056-54C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 13/45 | chr3 | 58109125 | ||||||
| chr3:58109535
|
A | G | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2200-41A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 14/45 | chr3 | 58109535 | ||||||
| chr3:58109739
|
G | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2323+40G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 15/45 | chr3 | 58109739 | ||||||
| chr3:58109772
|
T | C | 6 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0009t0004g0009others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2323+73T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 15/45 | chr3 | 58109772 | ||||||
| chr3:58109773
|
G | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 126 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2323+74G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 15/45 | chr3 | 58109773 | ||||||
| chr3:58110218
|
T | G | 9 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(6): Show | 9 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2484+48T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110218 | ||||||
| chr3:58110250
|
T | C | 1 | a0002c0004t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2484+80T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110250 | ||||||
| chr3:58110437
|
T | A | 1 | a0014c0023t0001g0081 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2484+267T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110437 | ||||||
| chr3:58110457
|
A | AT | 12 | a0001c0001t0001g0042a0002c0003t0001g0134a0002c0003t0002g0052others(9): Show | 12 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2484+297dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr3 | 58110457 | |||||
| chr3:58110535
|
C | G | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2484+365C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110535 | ||||||
| chr3:58110596
|
C | T | 1 | a0002c0008t0014g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2484+426C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110596 | ||||||
| chr3:58110625
|
T | C | 2 | a0003c0005t0001g0043a0003c0005t0001g0044 | 2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2484+455T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110625 | ||||||
| chr3:58110662
|
T | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.2484+492T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110662 | ||||||
| chr3:58110797
|
T | C | 35 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(32): Show | 35 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.2484+627T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58110797 | ||||||
| chr3:58111225
|
AAG | A | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2485-560_2485-559d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | INFO_REALIGN_3_PRIME | chr3 | 58111225 | |||||
| chr3:58111448
|
C | T | 2 | a0004c0006t0002g0050a0004c0043t0002g0049 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2485-343C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111448 | ||||||
| chr3:58111481
|
G | A | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2485-310G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111481 | ||||||
| chr3:58111487
|
G | C | 8 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0009t0004g0009others(5): Show | 8 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2485-304G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111487 | ||||||
| chr3:58111621
|
A | G | 2 | a0003c0035t0003g0060a0003c0054t0013g0108 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2485-170A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111621 | ||||||
| chr3:58111630
|
C | T | 27 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0005t0001g0029others(24): Show | 27 | HG00438.hp2 HG01109.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.2485-161C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111630 | ||||||
| chr3:58111669
|
T | C | 8 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(5): Show | 8 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2485-122T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 16/45 | chr3 | 58111669 | ||||||
| chr3:58112461
|
T | A | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2745+143T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112461 | ||||||
| chr3:58112521
|
T | C | 4 | a0002c0004t0002g0072a0002c0004t0002g0074a0002c0004t0002g0130others(1): Show | 4 | HG01257.hp1 HG03239.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2745+203T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112521 | ||||||
| chr3:58112689
|
G | A | 1 | a0003c0005t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2745+371G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112689 | ||||||
| chr3:58112717
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2745+399T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112717 | ||||||
| chr3:58112892
|
T | G | 1 | a0003c0005t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2745+574T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112892 | ||||||
| chr3:58112928
|
C | G | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2745+610C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58112928 | ||||||
| chr3:58113035
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2745+717G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113035 | ||||||
| chr3:58113211
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2745+893G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113211 | ||||||
| chr3:58113238
|
G | A | 8 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0021t0001g0121others(5): Show | 8 | HG01255.hp1 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2745+920G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113238 | ||||||
| chr3:58113387
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(26): Show | 29 | HG00408.hp2 HG01081.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2745+1069G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113387 | ||||||
| chr3:58113450
|
T | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2745+1132T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113450 | ||||||
| chr3:58113455
|
A | C | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2745+1137A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113455 | ||||||
| chr3:58113456
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2745+1138G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113456 | ||||||
| chr3:58113671
|
T | C | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2745+1353T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113671 | ||||||
| chr3:58113824
|
A | C | 4 | a0002c0003t0002g0138a0002c0003t0002g0139a0002c0003t0002g0140others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2745+1506A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113824 | ||||||
| chr3:58113948
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2745+1630A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58113948 | ||||||
| chr3:58114042
|
G | A | 1 | a0002c0004t0001g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2745+1724G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114042 | ||||||
| chr3:58114053
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2745+1735T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114053 | ||||||
| chr3:58114175
|
G | A | 1 | a0002c0003t0002g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2745+1857G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114175 | ||||||
| chr3:58114470
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0040 | 2 | HG03927.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.2745+2152C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114470 | ||||||
| chr3:58114547
|
A | C | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2745+2229A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114547 | ||||||
| chr3:58114549
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2745+2231C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114549 | ||||||
| chr3:58114551
|
C | CA | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2745+2233_2745+223 others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114551 | ||||||
| chr3:58114573
|
A | G | 1 | a0002c0002t0002g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2745+2255A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114573 | ||||||
| chr3:58114689
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2745+2371A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114689 | ||||||
| chr3:58114696
|
G | GT | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2745+2386dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr3 | 58114696 | |||||
| chr3:58114707
|
G | GT | 22 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0143others(19): Show | 22 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2745+2401dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr3 | 58114707 | |||||
| chr3:58114717
|
T | G | 5 | a0002c0002t0002g0120a0011c0056t0001g0112a0013c0022t0001g0116others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2745+2399T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114717 | ||||||
| chr3:58114718
|
TTG | T | 10 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2745+2402_2745+240 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr3 | 58114718 | |||||
| chr3:58114719
|
TG | T | 18 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(15): Show | 18 | HG00438.hp2 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2745+2402delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114719 | ||||||
| chr3:58114720
|
G | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2745+2402G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114720 | ||||||
| chr3:58114723
|
G | T | 1 | a0001c0030t0003g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2745+2405G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58114723 | ||||||
| chr3:58115008
|
G | C | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2745+2690G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115008 | ||||||
| chr3:58115024
|
G | A | 10 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2745+2706G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115024 | ||||||
| chr3:58115042
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2745+2724C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115042 | ||||||
| chr3:58115125
|
A | G | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2745+2807A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115125 | ||||||
| chr3:58115290
|
A | G | 3 | a0003c0035t0003g0060a0003c0054t0013g0108a0004c0006t0012g0109 | 3 | HG03471.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2745+2972A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115290 | ||||||
| chr3:58115438
|
A | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0004c0006t0002g0068others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2745+3120A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115438 | ||||||
| chr3:58115466
|
A | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2745+3148A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115466 | ||||||
| chr3:58115534
|
G | T | 10 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2745+3216G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115534 | ||||||
| chr3:58115734
|
G | A | 14 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0009t0004g0009others(11): Show | 14 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2746-3138G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115734 | ||||||
| chr3:58115739
|
C | T | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2746-3133C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115739 | ||||||
| chr3:58115744
|
G | A | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2746-3128G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115744 | ||||||
| chr3:58115782
|
ACCCACAA others(1): Show |
A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2746-3080_2746-307 others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr3 | 58115782 | |||||
| chr3:58115828
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.2746-3044T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58115828 | ||||||
| chr3:58116075
|
C | T | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2746-2797C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116075 | ||||||
| chr3:58116250
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0040 | 2 | HG03927.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.2746-2622A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116250 | ||||||
| chr3:58116326
|
A | C | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2746-2546A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116326 | ||||||
| chr3:58116357
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2746-2515G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116357 | ||||||
| chr3:58116398
|
G | A | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2746-2474G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116398 | ||||||
| chr3:58116435
|
G | A | 10 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.2746-2437G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116435 | ||||||
| chr3:58116515
|
G | T | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2746-2357G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116515 | ||||||
| chr3:58116622
|
G | A | 1 | a0002c0004t0002g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2746-2250G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116622 | ||||||
| chr3:58116834
|
G | A | 35 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2746-2038G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116834 | ||||||
| chr3:58116933
|
C | T | 32 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2746-1939C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58116933 | ||||||
| chr3:58117096
|
C | G | 6 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0009t0004g0009others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2746-1776C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117096 | ||||||
| chr3:58117130
|
C | T | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2746-1742C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117130 | ||||||
| chr3:58117364
|
G | C | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2746-1508G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117364 | ||||||
| chr3:58117531
|
G | C | 6 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0009t0004g0009others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2746-1341G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117531 | ||||||
| chr3:58117555
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2746-1317G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117555 | ||||||
| chr3:58117569
|
C | T | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2746-1303C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117569 | ||||||
| chr3:58117790
|
GT | G | 17 | a0001c0001t0001g0146a0002c0007t0002g0164a0002c0007t0002g0174others(14): Show | 17 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2746-1067delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | INFO_REALIGN_3_PRIME | chr3 | 58117790 | |||||
| chr3:58117917
|
T | C | 32 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2746-955T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117917 | ||||||
| chr3:58117951
|
C | T | 9 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(6): Show | 9 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746-921C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58117951 | ||||||
| chr3:58118005
|
G | C | 32 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2746-867G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58118005 | ||||||
| chr3:58118169
|
G | A | 1 | a0002c0003t0002g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2746-703G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58118169 | ||||||
| chr3:58118237
|
G | A | 32 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2746-635G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58118237 | ||||||
| chr3:58118309
|
A | G | 3 | a0013c0022t0001g0116a0020c0052t0001g0117a0026c0038t0002g0158 | 3 | HG02630.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2746-563A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58118309 | ||||||
| chr3:58118545
|
A | G | 1 | a0027c0039t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2746-327A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 18/45 | chr3 | 58118545 | ||||||
| chr3:58119150
|
G | A | 31 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(28): Show | 31 | HG00280.hp2 HG00438.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2863+161G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119150 | ||||||
| chr3:58119439
|
A | G | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2863+450A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119439 | ||||||
| chr3:58119462
|
T | C | 2 | a0003c0035t0003g0060a0003c0054t0013g0108 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2863+473T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119462 | ||||||
| chr3:58119692
|
C | A | 9 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(6): Show | 9 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2863+703C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119692 | ||||||
| chr3:58119934
|
A | C | 4 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863+945A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119934 | ||||||
| chr3:58119941
|
C | T | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2863+952C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58119941 | ||||||
| chr3:58120049
|
C | T | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863+1060C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58120049 | ||||||
| chr3:58120059
|
G | A | 1 | a0023c0033t0001g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2863+1070G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58120059 | ||||||
| chr3:58120268
|
C | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2864-973C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58120268 | ||||||
| chr3:58120375
|
G | A | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2864-866G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58120375 | ||||||
| chr3:58121169
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2864-72C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 19/45 | chr3 | 58121169 | ||||||
| chr3:58121817
|
C | T | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3126+314C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58121817 | ||||||
| chr3:58121935
|
C | T | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.3126+432C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58121935 | ||||||
| chr3:58121941
|
G | A | 3 | a0008c0013t0001g0066a0008c0013t0011g0180a0027c0039t0001g0067 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3126+438G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58121941 | ||||||
| chr3:58122065
|
A | C | 1 | a0002c0012t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3126+562A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122065 | ||||||
| chr3:58122101
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3126+598G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122101 | ||||||
| chr3:58122168
|
C | CA | 10 | a0002c0002t0002g0163a0003c0005t0001g0080a0003c0009t0004g0009others(7): Show | 10 | HG01169.hp1 HG01192.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.3126+684dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr3 | 58122168 | |||||
| chr3:58122168
|
CA | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00408.hp1 HG00408.hp2 HG01071.hp1 others(91): Show |
intron_variant | MODIFIER | c.3126+684delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr3 | 58122168 | |||||
| chr3:58122223
|
C | T | 3 | a0002c0015t0003g0025a0002c0020t0003g0123a0017c0046t0003g0015 | 3 | HG01109.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3126+720C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122223 | ||||||
| chr3:58122272
|
A | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.3126+769A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122272 | ||||||
| chr3:58122429
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3127-664G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122429 | ||||||
| chr3:58122496
|
CA | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.3127-581delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | INFO_REALIGN_3_PRIME | chr3 | 58122496 | |||||
| chr3:58122788
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3127-305T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122788 | ||||||
| chr3:58122816
|
G | T | 4 | a0002c0003t0002g0138a0002c0003t0002g0139a0002c0003t0002g0140others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.3127-277G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122816 | ||||||
| chr3:58122823
|
T | G | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3127-270T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122823 | ||||||
| chr3:58122824
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3127-269T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122824 | ||||||
| chr3:58122863
|
G | A | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3127-230G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 20/45 | chr3 | 58122863 | ||||||
| chr3:58123702
|
TTAA | T | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3724+13_3724+15del others(3): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58123702 | ||||||
| chr3:58123703
|
TA | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.3724+36delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | INFO_REALIGN_3_PRIME | chr3 | 58123703 | |||||
| chr3:58123703
|
TAA | T | 8 | a0001c0001t0001g0027a0003c0009t0004g0009a0003c0009t0004g0026others(5): Show | 8 | HG01169.hp1 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3724+35_3724+36del others(2): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | INFO_REALIGN_3_PRIME | chr3 | 58123703 | |||||
| chr3:58123806
|
C | T | 6 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(3): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3724+116C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58123806 | ||||||
| chr3:58124021
|
T | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.3725-311T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58124021 | ||||||
| chr3:58124045
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.3725-287A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58124045 | ||||||
| chr3:58124100
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3725-232G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58124100 | ||||||
| chr3:58124124
|
C | T | 7 | a0002c0002t0002g0160a0002c0002t0002g0163a0002c0004t0002g0069others(4): Show | 7 | HG01192.hp2 HG01257.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3725-208C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58124124 | ||||||
| chr3:58124140
|
C | T | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3725-192C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 21/45 | chr3 | 58124140 | ||||||
| chr3:58124533
|
C | G | 2 | a0002c0003t0001g0134a0002c0015t0001g0131 | 2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.3898+28C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124533 | ||||||
| chr3:58124621
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3898+116G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124621 | ||||||
| chr3:58124676
|
G | T | 6 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(3): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3898+171G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124676 | ||||||
| chr3:58124677
|
C | T | 6 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(3): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3898+172C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124677 | ||||||
| chr3:58124730
|
C | T | 1 | a0001c0027t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3898+225C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124730 | ||||||
| chr3:58124853
|
G | GA | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 125 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3898+356dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | INFO_REALIGN_3_PRIME | chr3 | 58124853 | |||||
| chr3:58124892
|
C | T | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3898+387C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58124892 | ||||||
| chr3:58125384
|
C | T | 8 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(5): Show | 8 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.3899-197C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125384 | ||||||
| chr3:58125401
|
G | A | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3899-180G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125401 | ||||||
| chr3:58125443
|
G | T | 1 | a0018c0050t0002g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3899-138G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125443 | ||||||
| chr3:58125496
|
A | G | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3899-85A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125496 | ||||||
| chr3:58125557
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3899-24G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125557 | ||||||
| chr3:58125558
|
T | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.3899-23T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 22/45 | chr3 | 58125558 | ||||||
| chr3:58126034
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.4061+291G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126034 | ||||||
| chr3:58126107
|
C | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.4061+364C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126107 | ||||||
| chr3:58126143
|
G | A | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4061+400G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126143 | ||||||
| chr3:58126148
|
G | A | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4061+405G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126148 | ||||||
| chr3:58126164
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4061+421G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126164 | ||||||
| chr3:58126335
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.4062-267G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126335 | ||||||
| chr3:58126390
|
AAAAT | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4062-207_4062-204d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | INFO_REALIGN_3_PRIME | chr3 | 58126390 | |||||
| chr3:58126524
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.4062-78A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126524 | ||||||
| chr3:58126597
|
T | G | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.4062-5T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 23/45 | chr3 | 58126597 | ||||||
| chr3:58126781
|
A | C | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4222+19A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58126781 | ||||||
| chr3:58126829
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 125 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.4222+67G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58126829 | ||||||
| chr3:58126926
|
AG | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4222+165delG | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58126926 | ||||||
| chr3:58127085
|
G | A | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4222+323G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127085 | ||||||
| chr3:58127094
|
A | G | 14 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(11): Show | 14 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.4222+332A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127094 | ||||||
| chr3:58127291
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.4222+529G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127291 | ||||||
| chr3:58127295
|
C | T | 3 | a0002c0002t0002g0125a0002c0002t0002g0147a0002c0002t0002g0150 | 3 | HG00280.hp1 HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4222+533C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127295 | ||||||
| chr3:58127325
|
C | CA | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4222+578dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | INFO_REALIGN_3_PRIME | chr3 | 58127325 | |||||
| chr3:58127336
|
A | G | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.4222+574A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127336 | ||||||
| chr3:58127790
|
G | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.4222+1028G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127790 | ||||||
| chr3:58127911
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.4222+1149T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127911 | ||||||
| chr3:58127915
|
G | A | 13 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(10): Show | 13 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.4222+1153G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58127915 | ||||||
| chr3:58128090
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4222+1328G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128090 | ||||||
| chr3:58128203
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.4222+1441G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128203 | ||||||
| chr3:58128249
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4222+1487G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128249 | ||||||
| chr3:58128270
|
C | G | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4222+1508C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128270 | ||||||
| chr3:58128568
|
T | C | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4222+1806T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128568 | ||||||
| chr3:58128928
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.4223-1813G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128928 | ||||||
| chr3:58128993
|
A | T | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-1748A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58128993 | ||||||
| chr3:58129036
|
C | T | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-1705C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129036 | ||||||
| chr3:58129090
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4223-1651G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129090 | ||||||
| chr3:58129157
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4223-1584C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129157 | ||||||
| chr3:58129313
|
G | C | 1 | a0025c0029t0001g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4223-1428G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129313 | ||||||
| chr3:58129411
|
G | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4223-1330G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129411 | ||||||
| chr3:58129487
|
A | G | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4223-1254A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129487 | ||||||
| chr3:58129607
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4223-1134G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129607 | ||||||
| chr3:58129744
|
A | C | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-997A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129744 | ||||||
| chr3:58129823
|
T | A | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4223-918T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129823 | ||||||
| chr3:58129886
|
T | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.4223-855T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129886 | ||||||
| chr3:58129887
|
G | A | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-854G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129887 | ||||||
| chr3:58129893
|
G | C | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4223-848G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129893 | ||||||
| chr3:58129998
|
G | C | 1 | a0001c0014t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4223-743G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58129998 | ||||||
| chr3:58130062
|
C | T | 1 | a0005c0010t0003g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4223-679C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130062 | ||||||
| chr3:58130084
|
C | T | 1 | a0022c0040t0001g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4223-657C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130084 | ||||||
| chr3:58130117
|
G | C | 1 | a0017c0046t0003g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4223-624G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130117 | ||||||
| chr3:58130302
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4223-439T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130302 | ||||||
| chr3:58130309
|
T | A | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-432T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130309 | ||||||
| chr3:58130313
|
T | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4223-428T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130313 | ||||||
| chr3:58130368
|
G | C | 2 | a0002c0003t0001g0134a0002c0015t0001g0131 | 2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.4223-373G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130368 | ||||||
| chr3:58130420
|
C | T | 2 | a0006c0017t0006g0057a0006c0049t0002g0023 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4223-321C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130420 | ||||||
| chr3:58130504
|
G | T | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4223-237G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130504 | ||||||
| chr3:58130557
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4223-184G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130557 | ||||||
| chr3:58130589
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.4223-152A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130589 | ||||||
| chr3:58130631
|
C | G | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4223-110C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130631 | ||||||
| chr3:58130631
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4223-110C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130631 | ||||||
| chr3:58130642
|
T | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4223-99T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130642 | ||||||
| chr3:58130655
|
G | C | 1 | a0003c0005t0001g0029 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4223-86G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130655 | ||||||
| chr3:58130693
|
G | T | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4223-48G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 24/45 | chr3 | 58130693 | ||||||
| chr3:58130916
|
T | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.4390+8T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58130916 | ||||||
| chr3:58130959
|
G | A | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4390+51G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58130959 | ||||||
| chr3:58131107
|
C | A | 6 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0006t0002g0068others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4390+199C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131107 | ||||||
| chr3:58131228
|
C | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.4390+320C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131228 | ||||||
| chr3:58131250
|
G | A | 2 | a0002c0012t0002g0118a0002c0012t0002g0152 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4390+342G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131250 | ||||||
| chr3:58131465
|
T | A | 2 | a0004c0021t0001g0121a0010c0057t0001g0046 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4390+557T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131465 | ||||||
| chr3:58131519
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4390+611A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131519 | ||||||
| chr3:58131648
|
T | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.4390+740T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131648 | ||||||
| chr3:58131734
|
G | A | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390+826G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131734 | ||||||
| chr3:58131769
|
T | G | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4390+861T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131769 | ||||||
| chr3:58131797
|
G | A | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4390+889G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131797 | ||||||
| chr3:58131937
|
G | A | 11 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.4391-871G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131937 | ||||||
| chr3:58131997
|
G | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0032others(11): Show | 14 | HG00408.hp2 HG01081.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.4391-811G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58131997 | ||||||
| chr3:58132097
|
C | T | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4391-711C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132097 | ||||||
| chr3:58132105
|
T | C | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4391-703T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132105 | ||||||
| chr3:58132163
|
C | T | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.4391-645C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132163 | ||||||
| chr3:58132188
|
G | T | 1 | a0006c0049t0002g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4391-620G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132188 | ||||||
| chr3:58132204
|
C | T | 6 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(3): Show | 6 | HG02572.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4391-604C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132204 | ||||||
| chr3:58132211
|
C | T | 1 | a0005c0037t0003g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4391-597C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132211 | ||||||
| chr3:58132212
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4391-596G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132212 | ||||||
| chr3:58132296
|
C | G | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4391-512C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132296 | ||||||
| chr3:58132425
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4391-383G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132425 | ||||||
| chr3:58132494
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | NA18957.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.4391-314T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | chr3 | 58132494 | ||||||
| chr3:58132516
|
T | TAA | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4391-291_4391-290i others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 25/45 | INFO_REALIGN_3_PRIME | chr3 | 58132516 | |||||
| chr3:58132973
|
A | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4514+42A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58132973 | ||||||
| chr3:58132977
|
GTCCACCC others(85): Show |
G | 2 | a0001c0001t0001g0045a0001c0001t0001g0137 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4514+79_4514+170de others(93): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58132977 | |||||
| chr3:58132983
|
CCATCCAT others(53): Show |
C | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4514+79_4514+138de others(61): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58132983 | |||||
| chr3:58133053
|
C | T | 2 | a0001c0014t0001g0111a0001c0014t0001g0115 | 2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4514+122C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133053 | ||||||
| chr3:58133065
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4514+134A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133065 | ||||||
| chr3:58133208
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4514+277A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133208 | ||||||
| chr3:58133231
|
G | T | 11 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.4514+300G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133231 | ||||||
| chr3:58133239
|
C | T | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4514+308C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133239 | ||||||
| chr3:58133419
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4514+488C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133419 | ||||||
| chr3:58133435
|
T | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.4514+504T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133435 | ||||||
| chr3:58133437
|
G | GA | 15 | a0002c0002t0002g0064a0002c0002t0002g0162a0002c0002t0002g0163others(12): Show | 15 | HG00738.hp2 HG01106.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.4514+534dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133437
|
GAA | G | 8 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(5): Show | 8 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.4514+533_4514+534d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133437
|
GAAA | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0094others(5): Show | 8 | HG00438.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.4514+532_4514+534d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133437
|
GAAAA | G | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00408.hp1 HG00408.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.4514+531_4514+534d others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133437
|
GAAAAA | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0040a0006c0017t0006g0024others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4514+530_4514+534d others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133437
|
GAAAAAAA | G | 11 | a0005c0010t0002g0013a0005c0010t0002g0065a0005c0010t0003g0002others(8): Show | 11 | HG02451.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.4514+528_4514+534d others(9): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | INFO_REALIGN_3_PRIME | chr3 | 58133437 | |||||
| chr3:58133442
|
A | G | 5 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4514+511A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133442 | ||||||
| chr3:58133443
|
A | G | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4514+512A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133443 | ||||||
| chr3:58133499
|
T | G | 9 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4514+568T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133499 | ||||||
| chr3:58133544
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4514+613C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133544 | ||||||
| chr3:58133553
|
AGTT | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.4514+623_4514+625d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58133553 | ||||||
| chr3:58134139
|
G | A | 2 | a0002c0002t0002g0165a0002c0002t0002g0166 | 2 | HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4515-477G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58134139 | ||||||
| chr3:58134155
|
G | C | 10 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(7): Show | 10 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4515-461G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 26/45 | chr3 | 58134155 | ||||||
| chr3:58134783
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4671+11G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58134783 | ||||||
| chr3:58134926
|
G | T | 8 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(5): Show | 8 | HG01891.hp1 HG02572.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.4671+154G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58134926 | ||||||
| chr3:58134983
|
T | C | 1 | a0020c0052t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4671+211T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58134983 | ||||||
| chr3:58135146
|
T | A | 1 | a0003c0005t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4671+374T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135146 | ||||||
| chr3:58135347
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4671+575C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135347 | ||||||
| chr3:58135379
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0092others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4672-600A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135379 | ||||||
| chr3:58135595
|
T | C | 10 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.4672-384T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135595 | ||||||
| chr3:58135899
|
T | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.4672-80T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135899 | ||||||
| chr3:58135968
|
A | G | 1 | a0004c0006t0002g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4672-11A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 27/45 | chr3 | 58135968 | ||||||
| chr3:58136221
|
C | T | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4861+53C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136221 | ||||||
| chr3:58136255
|
C | T | 2 | a0002c0003t0001g0134a0002c0015t0001g0131 | 2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.4861+87C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136255 | ||||||
| chr3:58136310
|
G | A | 10 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(7): Show | 10 | HG01891.hp1 HG02572.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.4861+142G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136310 | ||||||
| chr3:58136433
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.4861+265T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136433 | ||||||
| chr3:58136746
|
C | CT | 24 | a0002c0007t0002g0164a0002c0007t0002g0175a0002c0007t0002g0177others(21): Show | 24 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4861+601dupT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
C | CTTTTT | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 80 | HG00408.hp1 HG00438.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.4861+597_4861+601d others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
C | CTTTTTT | 8 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG00408.hp2 HG01123.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.4861+596_4861+601d others(8): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
C | CTTTTTTT others(3): Show |
1 | a0003c0005t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4861+592_4861+601d others(12): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
C | CTTTTTTT others(18): Show |
2 | a0003c0009t0004g0009a0003c0009t0004g0026 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4861+601_4861+602i others(27): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
C | CTTTTTTT others(20): Show |
1 | a0003c0009t0004g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4861+601_4861+602i others(29): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136746
|
CTT | C | 7 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(4): Show | 7 | HG01891.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4861+600_4861+601d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58136746 | |||||
| chr3:58136882
|
G | A | 2 | a0006c0017t0006g0057a0006c0049t0002g0023 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4861+714G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136882 | ||||||
| chr3:58136941
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4861+773G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58136941 | ||||||
| chr3:58137012
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4861+844G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137012 | ||||||
| chr3:58137100
|
C | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4861+932C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137100 | ||||||
| chr3:58137131
|
TAAG | T | 11 | a0004c0006t0002g0048a0004c0006t0002g0050a0004c0006t0002g0068others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.4861+968_4861+970d others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58137131 | |||||
| chr3:58137181
|
G | A | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4861+1013G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137181 | ||||||
| chr3:58137243
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4862-1039G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137243 | ||||||
| chr3:58137279
|
A | G | 11 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(8): Show | 11 | HG01891.hp1 HG02040.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.4862-1003A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137279 | ||||||
| chr3:58137325
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4862-957G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137325 | ||||||
| chr3:58137522
|
C | A | 44 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.4862-760C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137522 | ||||||
| chr3:58137626
|
T | A | 1 | a0002c0004t0002g0170 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4862-656T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137626 | ||||||
| chr3:58137774
|
C | A | 1 | a0003c0005t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4862-508C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137774 | ||||||
| chr3:58137816
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.4862-466C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | chr3 | 58137816 | ||||||
| chr3:58138252
|
TC | T | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4862-28delC | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 28/45 | INFO_REALIGN_3_PRIME | chr3 | 58138252 | |||||
| chr3:58138588
|
G | A | 1 | a0002c0002t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5109+59G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58138588 | ||||||
| chr3:58138683
|
A | G | 7 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(4): Show | 7 | HG00438.hp2 HG02735.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.5109+154A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58138683 | ||||||
| chr3:58138743
|
C | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5109+214C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58138743 | ||||||
| chr3:58138766
|
A | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5109+237A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58138766 | ||||||
| chr3:58138853
|
AAC | A | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.5109+326_5109+327d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | INFO_REALIGN_3_PRIME | chr3 | 58138853 | |||||
| chr3:58138872
|
C | T | 10 | a0003c0005t0001g0029a0003c0005t0001g0043a0003c0005t0001g0044others(7): Show | 10 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.5109+343C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58138872 | ||||||
| chr3:58139019
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5109+490T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139019 | ||||||
| chr3:58139060
|
T | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5109+531T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139060 | ||||||
| chr3:58139080
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5109+551C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139080 | ||||||
| chr3:58139271
|
G | A | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5109+742G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139271 | ||||||
| chr3:58139425
|
A | C | 4 | a0011c0056t0001g0112a0013c0022t0001g0116a0015c0024t0002g0012others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.5109+896A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139425 | ||||||
| chr3:58139456
|
G | A | 9 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(6): Show | 9 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.5109+927G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139456 | ||||||
| chr3:58139726
|
G | T | 10 | a0002c0015t0003g0025a0002c0020t0003g0123a0005c0011t0003g0011others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.5109+1197G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58139726 | ||||||
| chr3:58140244
|
G | T | 28 | a0001c0031t0005g0145a0002c0003t0001g0134a0002c0003t0002g0052others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.5110-1614G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140244 | ||||||
| chr3:58140259
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.5110-1599C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140259 | ||||||
| chr3:58140370
|
C | T | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5110-1488C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140370 | ||||||
| chr3:58140444
|
C | T | 1 | a0002c0044t0001g0167 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.5110-1414C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140444 | ||||||
| chr3:58140496
|
A | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.5110-1362A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140496 | ||||||
| chr3:58140548
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5110-1310C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140548 | ||||||
| chr3:58140694
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5110-1164C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140694 | ||||||
| chr3:58140772
|
C | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5110-1086C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140772 | ||||||
| chr3:58140820
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5110-1038G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140820 | ||||||
| chr3:58140821
|
C | G | 18 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(15): Show | 18 | HG00438.hp2 HG01891.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.5110-1037C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58140821 | ||||||
| chr3:58141085
|
C | CA | 12 | a0002c0003t0007g0127a0003c0005t0001g0029a0003c0005t0001g0043others(9): Show | 12 | HG00438.hp2 HG02280.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-761dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | INFO_REALIGN_3_PRIME | chr3 | 58141085 | |||||
| chr3:58141095
|
A | T | 2 | a0002c0002t0002g0124a0002c0004t0001g0156 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.5110-763A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58141095 | ||||||
| chr3:58141248
|
G | C | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5110-610G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58141248 | ||||||
| chr3:58141674
|
CTG | C | 3 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110 | 3 | HG02922.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5110-183_5110-182d others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 29/45 | chr3 | 58141674 | ||||||
| chr3:58142090
|
G | A | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5181+161G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 30/45 | chr3 | 58142090 | ||||||
| chr3:58142100
|
C | T | 25 | a0001c0031t0005g0145a0002c0003t0001g0134a0002c0003t0002g0052others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.5181+171C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 30/45 | chr3 | 58142100 | ||||||
| chr3:58142255
|
T | C | 1 | a0002c0051t0008g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5181+326T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 30/45 | chr3 | 58142255 | ||||||
| chr3:58142451
|
T | A | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5182-199T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 30/45 | chr3 | 58142451 | ||||||
| chr3:58142522
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5182-128A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 30/45 | chr3 | 58142522 | ||||||
| chr3:58142983
|
T | G | 3 | a0002c0036t0009g0075a0013c0022t0001g0116a0026c0038t0002g0158 | 3 | HG02040.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5284+231T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58142983 | ||||||
| chr3:58143048
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5284+296T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58143048 | ||||||
| chr3:58143202
|
G | C | 43 | a0001c0031t0005g0145a0002c0003t0001g0134a0002c0003t0002g0052others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.5285-271G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58143202 | ||||||
| chr3:58143241
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5285-232G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58143241 | ||||||
| chr3:58143242
|
A | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5285-231A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58143242 | ||||||
| chr3:58143292
|
G | A | 1 | a0002c0051t0008g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5285-181G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | chr3 | 58143292 | ||||||
| chr3:58143293
|
GA | G | 11 | a0002c0003t0001g0134a0002c0003t0002g0052a0002c0003t0002g0133others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.5285-168delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 31/45 | INFO_REALIGN_3_PRIME | chr3 | 58143293 | |||||
| chr3:58143627
|
G | T | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5425+14G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143627 | ||||||
| chr3:58143689
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5425+76G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143689 | ||||||
| chr3:58143722
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5425+109G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143722 | ||||||
| chr3:58143723
|
A | G | 44 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.5425+110A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143723 | ||||||
| chr3:58143953
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5425+340G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143953 | ||||||
| chr3:58143958
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5425+345A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143958 | ||||||
| chr3:58143974
|
C | T | 2 | a0011c0056t0001g0112a0015c0024t0002g0012 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5425+361C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58143974 | ||||||
| chr3:58143979
|
G | GTGGAAGA others(16): Show |
2 | a0001c0030t0003g0128a0004c0043t0002g0049 | 2 | HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.5425+391_5425+413d others(25): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | INFO_REALIGN_3_PRIME | chr3 | 58143979 | |||||
| chr3:58143979
|
GTGGAAGA others(16): Show |
G | 1 | a0001c0014t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5425+391_5425+413d others(25): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | INFO_REALIGN_3_PRIME | chr3 | 58143979 | |||||
| chr3:58144028
|
T | G | 23 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(20): Show | 23 | HG00438.hp2 HG01255.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.5425+415T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144028 | ||||||
| chr3:58144441
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0027others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.5425+828A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144441 | ||||||
| chr3:58144549
|
G | C | 43 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.5425+936G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144549 | ||||||
| chr3:58144607
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5425+994G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144607 | ||||||
| chr3:58144659
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5425+1046G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144659 | ||||||
| chr3:58144763
|
A | G | 4 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5425+1150A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144763 | ||||||
| chr3:58144787
|
G | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-1134G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144787 | ||||||
| chr3:58144869
|
C | A | 4 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5426-1052C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144869 | ||||||
| chr3:58144872
|
T | C | 21 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0007g0127others(18): Show | 21 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.5426-1049T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144872 | ||||||
| chr3:58144961
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-960T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144961 | ||||||
| chr3:58144973
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-948G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58144973 | ||||||
| chr3:58145022
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-899G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145022 | ||||||
| chr3:58145116
|
C | T | 1 | a0002c0008t0014g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5426-805C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145116 | ||||||
| chr3:58145212
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-709G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145212 | ||||||
| chr3:58145252
|
T | G | 1 | a0002c0007t0002g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5426-669T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145252 | ||||||
| chr3:58145449
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5426-472A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145449 | ||||||
| chr3:58145475
|
A | G | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5426-446A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145475 | ||||||
| chr3:58145649
|
G | GAT | 7 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(4): Show | 7 | HG01891.hp1 HG02040.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.5426-272_5426-271i others(4): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145649 | ||||||
| chr3:58145685
|
C | T | 3 | a0002c0002t0002g0125a0002c0002t0002g0147a0002c0002t0002g0150 | 3 | HG00280.hp1 HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.5426-236C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145685 | ||||||
| chr3:58145729
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5426-192T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145729 | ||||||
| chr3:58145755
|
G | C | 1 | a0024c0032t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5426-166G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145755 | ||||||
| chr3:58145773
|
G | A | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5426-148G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145773 | ||||||
| chr3:58145788
|
C | T | 32 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(29): Show | 32 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.5426-133C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145788 | ||||||
| chr3:58145871
|
G | A | 3 | a0008c0013t0001g0066a0008c0013t0011g0180a0027c0039t0001g0067 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5426-50G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 32/45 | chr3 | 58145871 | ||||||
| chr3:58146144
|
C | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5554+95C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 33/45 | chr3 | 58146144 | ||||||
| chr3:58146156
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5554+107T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 33/45 | chr3 | 58146156 | ||||||
| chr3:58146252
|
C | T | 36 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.5554+203C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 33/45 | chr3 | 58146252 | ||||||
| chr3:58146541
|
G | A | 2 | a0002c0007t0002g0175a0002c0007t0002g0177 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.5555-279G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 33/45 | chr3 | 58146541 | ||||||
| chr3:58146653
|
G | A | 3 | a0001c0031t0005g0145a0005c0048t0005g0001a0020c0052t0001g0117 | 3 | HG02559.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5555-167G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 33/45 | chr3 | 58146653 | ||||||
| chr3:58147081
|
G | A | 24 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(21): Show | 24 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.5728+88G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147081 | ||||||
| chr3:58147082
|
C | T | 24 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(21): Show | 24 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.5728+89C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147082 | ||||||
| chr3:58147088
|
G | A | 4 | a0002c0036t0009g0075a0006c0017t0006g0024a0006c0017t0006g0057others(1): Show | 4 | HG02040.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.5728+95G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147088 | ||||||
| chr3:58147194
|
C | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5728+201C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147194 | ||||||
| chr3:58147449
|
C | T | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5728+456C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147449 | ||||||
| chr3:58147559
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5728+566A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147559 | ||||||
| chr3:58147683
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5729-523A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147683 | ||||||
| chr3:58147721
|
C | T | 7 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(4): Show | 7 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.5729-485C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147721 | ||||||
| chr3:58147963
|
T | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5729-243T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58147963 | ||||||
| chr3:58148072
|
G | C | 8 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.5729-134G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | chr3 | 58148072 | ||||||
| chr3:58148076
|
AT | A | 43 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.5729-121delT | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 34/45 | INFO_REALIGN_3_PRIME | chr3 | 58148076 | |||||
| chr3:58148460
|
A | C | 1 | a0002c0002t0002g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5887+96A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/45 | chr3 | 58148460 | ||||||
| chr3:58148494
|
C | T | 1 | a0026c0038t0002g0158 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5887+130C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/45 | chr3 | 58148494 | ||||||
| chr3:58148544
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5888-105G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/45 | chr3 | 58148544 | ||||||
| chr3:58148553
|
C | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5888-96C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 35/45 | chr3 | 58148553 | ||||||
| chr3:58148902
|
T | G | 5 | a0002c0008t0002g0022a0002c0008t0002g0155a0002c0008t0014g0110others(2): Show | 5 | HG01891.hp1 HG02040.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.6091+50T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58148902 | ||||||
| chr3:58149024
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6091+172G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149024 | ||||||
| chr3:58149228
|
C | T | 8 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.6091+376C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149228 | ||||||
| chr3:58149394
|
G | A | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6092-456G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149394 | ||||||
| chr3:58149452
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6092-398T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149452 | ||||||
| chr3:58149526
|
C | T | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6092-324C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149526 | ||||||
| chr3:58149611
|
C | T | 3 | a0001c0031t0005g0145a0005c0048t0005g0001a0020c0052t0001g0117 | 3 | HG02559.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6092-239C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 36/45 | chr3 | 58149611 | ||||||
| chr3:58150006
|
T | G | 1 | a0005c0048t0005g0001 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.6244+4T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 37/45 | chr3 | 58150006 | ||||||
| chr3:58150324
|
C | T | 6 | a0002c0036t0009g0075a0006c0017t0006g0024a0006c0017t0006g0057others(3): Show | 6 | HG02040.hp1 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.6367+97C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150324 | ||||||
| chr3:58150336
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6367+109C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150336 | ||||||
| chr3:58150698
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6367+471G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150698 | ||||||
| chr3:58150702
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.6367+475T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150702 | ||||||
| chr3:58150887
|
G | A | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6367+660G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150887 | ||||||
| chr3:58150945
|
A | G | 6 | a0002c0036t0009g0075a0006c0017t0006g0024a0006c0017t0006g0057others(3): Show | 6 | HG02040.hp1 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.6367+718A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58150945 | ||||||
| chr3:58151005
|
A | C | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6367+778A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151005 | ||||||
| chr3:58151034
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0137 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.6367+807G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151034 | ||||||
| chr3:58151085
|
T | C | 2 | a0013c0022t0001g0116a0026c0038t0002g0158 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6367+858T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151085 | ||||||
| chr3:58151212
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6367+985C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151212 | ||||||
| chr3:58151251
|
G | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0150 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.6367+1024G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151251 | ||||||
| chr3:58151253
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6367+1026G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151253 | ||||||
| chr3:58151308
|
C | G | 3 | a0006c0017t0006g0024a0006c0017t0006g0057a0006c0049t0002g0023 | 3 | HG02572.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6367+1081C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151308 | ||||||
| chr3:58151352
|
G | A | 1 | a0002c0004t0002g0170 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6367+1125G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151352 | ||||||
| chr3:58151391
|
C | CA | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6367+1188dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | INFO_REALIGN_3_PRIME | chr3 | 58151391 | |||||
| chr3:58151391
|
C | CAA | 10 | a0001c0001t0001g0041a0001c0031t0005g0145a0003c0035t0003g0060others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.6367+1187_6367+118 others(6): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | INFO_REALIGN_3_PRIME | chr3 | 58151391 | |||||
| chr3:58151391
|
CA | C | 17 | a0002c0002t0001g0176a0002c0002t0002g0078a0002c0002t0002g0166others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.6367+1188delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | INFO_REALIGN_3_PRIME | chr3 | 58151391 | |||||
| chr3:58151416
|
G | A | 11 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.6367+1189G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151416 | ||||||
| chr3:58151418
|
G | A | 14 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.6367+1191G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151418 | ||||||
| chr3:58151436
|
A | G | 54 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.6367+1209A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151436 | ||||||
| chr3:58151684
|
A | G | 17 | a0002c0015t0003g0025a0002c0020t0003g0123a0002c0036t0009g0075others(14): Show | 17 | HG01109.hp1 HG01891.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.6367+1457A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151684 | ||||||
| chr3:58151918
|
T | G | 1 | a0002c0002t0002g0006 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6368-1457T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151918 | ||||||
| chr3:58151996
|
A | G | 24 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(21): Show | 24 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.6368-1379A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58151996 | ||||||
| chr3:58152452
|
G | A | 1 | a0003c0009t0004g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6368-923G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58152452 | ||||||
| chr3:58152550
|
GA | G | 15 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(12): Show | 15 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.6368-824delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58152550 | ||||||
| chr3:58152801
|
G | A | 24 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(21): Show | 24 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.6368-574G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58152801 | ||||||
| chr3:58152982
|
C | T | 14 | a0002c0015t0003g0025a0002c0020t0003g0123a0002c0036t0009g0075others(11): Show | 14 | HG01109.hp1 HG01891.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.6368-393C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58152982 | ||||||
| chr3:58153061
|
C | T | 4 | a0001c0001t0001g0059a0001c0014t0001g0111a0001c0014t0001g0115others(1): Show | 4 | HG02109.hp2 HG03579.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.6368-314C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58153061 | ||||||
| chr3:58153220
|
G | T | 1 | a0005c0010t0002g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6368-155G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58153220 | ||||||
| chr3:58153263
|
G | A | 3 | a0001c0031t0005g0145a0005c0048t0005g0001a0020c0052t0001g0117 | 3 | HG02559.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6368-112G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 38/45 | chr3 | 58153263 | ||||||
| chr3:58153670
|
G | T | 13 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6634+29G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58153670 | ||||||
| chr3:58153675
|
G | A | 13 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6634+34G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58153675 | ||||||
| chr3:58153687
|
G | C | 1 | a0002c0008t0002g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6634+46G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58153687 | ||||||
| chr3:58154012
|
G | A | 1 | a0002c0004t0002g0170 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6634+371G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154012 | ||||||
| chr3:58154208
|
T | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.6634+567T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154208 | ||||||
| chr3:58154309
|
G | A | 15 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(12): Show | 15 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.6635-482G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154309 | ||||||
| chr3:58154398
|
A | G | 13 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6635-393A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154398 | ||||||
| chr3:58154509
|
C | G | 16 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(13): Show | 16 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.6635-282C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154509 | ||||||
| chr3:58154509
|
C | T | 13 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6635-282C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154509 | ||||||
| chr3:58154544
|
CA | C | 20 | a0001c0001t0001g0086a0001c0031t0005g0145a0002c0007t0002g0164others(17): Show | 20 | HG00280.hp2 HG01106.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.6635-230delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | INFO_REALIGN_3_PRIME | chr3 | 58154544 | |||||
| chr3:58154599
|
T | C | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6635-192T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154599 | ||||||
| chr3:58154618
|
T | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6635-173T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 39/45 | chr3 | 58154618 | ||||||
| chr3:58155041
|
G | A | 15 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(12): Show | 15 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.6772+113G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155041 | ||||||
| chr3:58155315
|
G | A | 16 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(13): Show | 16 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.6772+387G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155315 | ||||||
| chr3:58155353
|
G | A | 16 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(13): Show | 16 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.6772+425G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155353 | ||||||
| chr3:58155369
|
A | G | 2 | a0001c0001t0001g0005a0001c0019t0001g0122 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6772+441A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155369 | ||||||
| chr3:58155513
|
G | C | 2 | a0002c0003t0001g0134a0002c0015t0001g0131 | 2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.6773-447G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155513 | ||||||
| chr3:58155524
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6773-436A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155524 | ||||||
| chr3:58155536
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.6773-424G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155536 | ||||||
| chr3:58155540
|
C | T | 29 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(26): Show | 29 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.6773-420C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155540 | ||||||
| chr3:58155564
|
TA | T | 16 | a0001c0031t0005g0145a0002c0007t0002g0164a0002c0007t0002g0174others(13): Show | 16 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.6773-391delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | INFO_REALIGN_3_PRIME | chr3 | 58155564 | |||||
| chr3:58155584
|
T | C | 2 | a0006c0017t0006g0024a0006c0017t0006g0057 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.6773-376T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155584 | ||||||
| chr3:58155684
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6773-276A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155684 | ||||||
| chr3:58155716
|
G | C | 3 | a0001c0031t0005g0145a0005c0048t0005g0001a0020c0052t0001g0117 | 3 | HG02559.hp1 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6773-244G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155716 | ||||||
| chr3:58155759
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.6773-201C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155759 | ||||||
| chr3:58155761
|
C | T | 13 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.6773-199C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155761 | ||||||
| chr3:58155776
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6773-184G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155776 | ||||||
| chr3:58155922
|
A | C | 1 | a0002c0007t0002g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6773-38A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155922 | ||||||
| chr3:58155947
|
C | A | 1 | a0005c0037t0003g0129 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6773-13C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 40/45 | chr3 | 58155947 | ||||||
| chr3:58156109
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6888+34G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156109 | ||||||
| chr3:58156119
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.6888+44A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156119 | ||||||
| chr3:58156146
|
CTT | C | 11 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.6888+72_6888+73del others(2): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156146 | ||||||
| chr3:58156414
|
C | T | 10 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0007g0127others(7): Show | 10 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.6888+339C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156414 | ||||||
| chr3:58156501
|
A | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6888+426A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156501 | ||||||
| chr3:58156621
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6888+546G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156621 | ||||||
| chr3:58156708
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6888+633T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156708 | ||||||
| chr3:58156721
|
G | C | 1 | a0002c0002t0001g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6888+646G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156721 | ||||||
| chr3:58156737
|
C | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6888+662C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156737 | ||||||
| chr3:58156845
|
C | T | 13 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.6888+770C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156845 | ||||||
| chr3:58156941
|
C | T | 1 | a0002c0007t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6888+866C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156941 | ||||||
| chr3:58156994
|
G | T | 15 | a0001c0031t0005g0145a0002c0015t0003g0025a0002c0020t0003g0123others(12): Show | 15 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.6888+919G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58156994 | ||||||
| chr3:58157104
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6888+1029G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157104 | ||||||
| chr3:58157323
|
A | G | 1 | a0025c0029t0001g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6888+1248A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157323 | ||||||
| chr3:58157356
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6888+1281G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157356 | ||||||
| chr3:58157477
|
G | A | 1 | a0002c0008t0002g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6888+1402G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157477 | ||||||
| chr3:58157649
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6888+1574T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157649 | ||||||
| chr3:58157713
|
G | T | 51 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.6888+1638G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157713 | ||||||
| chr3:58157862
|
A | G | 1 | a0003c0005t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.6889-1692A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157862 | ||||||
| chr3:58157911
|
C | T | 1 | a0009c0034t0002g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.6889-1643C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58157911 | ||||||
| chr3:58158003
|
G | A | 8 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(5): Show | 8 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.6889-1551G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58158003 | ||||||
| chr3:58158014
|
CA | C | 15 | a0001c0031t0005g0145a0002c0015t0003g0025a0002c0020t0003g0123others(12): Show | 15 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.6889-1538delA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | INFO_REALIGN_3_PRIME | chr3 | 58158014 | |||||
| chr3:58158179
|
G | C | 7 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(4): Show | 7 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.6889-1375G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58158179 | ||||||
| chr3:58158500
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6889-1054G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58158500 | ||||||
| chr3:58158613
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.6889-941T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58158613 | ||||||
| chr3:58158733
|
T | G | 1 | a0001c0031t0005g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6889-821T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58158733 | ||||||
| chr3:58159064
|
A | G | 12 | a0001c0030t0003g0128a0003c0054t0013g0108a0004c0006t0002g0048others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.6889-490A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58159064 | ||||||
| chr3:58159151
|
A | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6889-403A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58159151 | ||||||
| chr3:58159431
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6889-123A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58159431 | ||||||
| chr3:58159536
|
G | A | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.6889-18G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 41/45 | chr3 | 58159536 | ||||||
| chr3:58159771
|
G | A | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7021+85G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58159771 | ||||||
| chr3:58160173
|
T | G | 1 | a0011c0056t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7021+487T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160173 | ||||||
| chr3:58160175
|
C | T | 11 | a0001c0030t0003g0128a0004c0006t0002g0048a0004c0006t0002g0050others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.7021+489C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160175 | ||||||
| chr3:58160293
|
C | T | 22 | a0001c0030t0003g0128a0002c0007t0002g0164a0002c0007t0002g0174others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.7021+607C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160293 | ||||||
| chr3:58160376
|
C | T | 11 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.7021+690C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160376 | ||||||
| chr3:58160515
|
T | A | 39 | a0001c0030t0003g0128a0001c0031t0005g0145a0002c0007t0002g0164others(36): Show | 39 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.7021+829T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160515 | ||||||
| chr3:58160597
|
G | T | 11 | a0001c0030t0003g0128a0004c0006t0002g0048a0004c0006t0002g0050others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.7021+911G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160597 | ||||||
| chr3:58160926
|
T | C | 1 | a0003c0035t0003g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7021+1240T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160926 | ||||||
| chr3:58160984
|
A | G | 25 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(22): Show | 25 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.7021+1298A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58160984 | ||||||
| chr3:58161078
|
G | A | 25 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0002g0052others(22): Show | 25 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.7021+1392G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161078 | ||||||
| chr3:58161133
|
G | C | 1 | a0001c0001t0001g0132 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.7021+1447G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161133 | ||||||
| chr3:58161216
|
T | C | 4 | a0001c0031t0005g0145a0005c0048t0005g0001a0006c0017t0006g0024others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7021+1530T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161216 | ||||||
| chr3:58161522
|
C | T | 33 | a0001c0030t0003g0128a0002c0007t0002g0164a0002c0007t0002g0174others(30): Show | 33 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.7022-1632C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161522 | ||||||
| chr3:58161695
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0056 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.7022-1459T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161695 | ||||||
| chr3:58161703
|
C | T | 37 | a0001c0030t0003g0128a0001c0031t0005g0145a0002c0007t0002g0164others(34): Show | 37 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.7022-1451C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161703 | ||||||
| chr3:58161754
|
CTGGCCTT others(16): Show |
C | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.7022-1372_7022-135 others(27): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | INFO_REALIGN_3_PRIME | chr3 | 58161754 | |||||
| chr3:58161879
|
G | T | 2 | a0006c0017t0006g0024a0006c0017t0006g0057 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7022-1275G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161879 | ||||||
| chr3:58161991
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | NA18957.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.7022-1163T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58161991 | ||||||
| chr3:58162006
|
T | C | 33 | a0001c0030t0003g0128a0002c0007t0002g0164a0002c0007t0002g0174others(30): Show | 33 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.7022-1148T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162006 | ||||||
| chr3:58162022
|
C | G | 1 | a0003c0005t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.7022-1132C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162022 | ||||||
| chr3:58162074
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7022-1080T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162074 | ||||||
| chr3:58162161
|
G | A | 62 | a0001c0030t0003g0128a0001c0031t0005g0145a0002c0002t0001g0176others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.7022-993G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162161 | ||||||
| chr3:58162331
|
A | G | 4 | a0001c0031t0005g0145a0005c0048t0005g0001a0006c0017t0006g0024others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7022-823A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162331 | ||||||
| chr3:58162336
|
G | A | 11 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0007g0127others(8): Show | 11 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.7022-818G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162336 | ||||||
| chr3:58162389
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0089 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.7022-765C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162389 | ||||||
| chr3:58162490
|
C | A | 1 | a0005c0011t0003g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7022-664C>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162490 | ||||||
| chr3:58162569
|
C | T | 4 | a0001c0031t0005g0145a0005c0048t0005g0001a0006c0017t0006g0024others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7022-585C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162569 | ||||||
| chr3:58162679
|
A | G | 4 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026others(1): Show | 4 | HG02280.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.7022-475A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 42/45 | chr3 | 58162679 | ||||||
| chr3:58163350
|
C | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7198+20C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163350 | ||||||
| chr3:58163426
|
G | A | 1 | a0003c0005t0001g0044 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.7198+96G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163426 | ||||||
| chr3:58163690
|
G | A | 22 | a0001c0030t0003g0128a0002c0007t0002g0164a0002c0007t0002g0174others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.7198+360G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163690 | ||||||
| chr3:58163710
|
G | A | 8 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.7198+380G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163710 | ||||||
| chr3:58163862
|
G | A | 16 | a0001c0001t0001g0094a0001c0031t0005g0145a0002c0015t0003g0025others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.7198+532G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163862 | ||||||
| chr3:58163939
|
AAAGTGAG others(825): Show |
A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7198+616_7198+1447 others(3): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr3 | 58163939 | |||||
| chr3:58163985
|
T | C | 15 | a0001c0031t0005g0145a0002c0015t0003g0025a0002c0020t0003g0123others(12): Show | 15 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.7198+655T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58163985 | ||||||
| chr3:58164113
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7198+783T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164113 | ||||||
| chr3:58164457
|
C | T | 8 | a0002c0007t0002g0164a0002c0007t0002g0174a0002c0007t0002g0175others(5): Show | 8 | HG00280.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.7198+1127C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164457 | ||||||
| chr3:58164488
|
C | T | 1 | a0003c0005t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7198+1158C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164488 | ||||||
| chr3:58164618
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.7198+1288C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164618 | ||||||
| chr3:58164626
|
T | A | 4 | a0001c0031t0005g0145a0005c0048t0005g0001a0006c0017t0006g0024others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7198+1296T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164626 | ||||||
| chr3:58164706
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.7198+1376C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164706 | ||||||
| chr3:58164850
|
C | T | 11 | a0001c0030t0003g0128a0004c0006t0002g0048a0004c0006t0002g0050others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.7198+1520C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58164850 | ||||||
| chr3:58165132
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7198+1802G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165132 | ||||||
| chr3:58165333
|
G | A | 1 | a0016c0025t0010g0031 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7198+2003G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165333 | ||||||
| chr3:58165681
|
C | T | 1 | a0014c0023t0001g0081 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.7198+2351C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165681 | ||||||
| chr3:58165779
|
G | A | 8 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.7198+2449G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165779 | ||||||
| chr3:58165792
|
A | C | 33 | a0001c0030t0003g0128a0002c0007t0002g0164a0002c0007t0002g0174others(30): Show | 33 | HG00280.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.7198+2462A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165792 | ||||||
| chr3:58165815
|
T | G | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.7198+2485T>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165815 | ||||||
| chr3:58165834
|
C | T | 8 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.7198+2504C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165834 | ||||||
| chr3:58165883
|
G | A | 1 | a0006c0017t0006g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7198+2553G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165883 | ||||||
| chr3:58165903
|
G | A | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7199-2537G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58165903 | ||||||
| chr3:58166000
|
G | A | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.7199-2440G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166000 | ||||||
| chr3:58166119
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.7199-2321T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166119 | ||||||
| chr3:58166220
|
C | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.7199-2220C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166220 | ||||||
| chr3:58166295
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7199-2145T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166295 | ||||||
| chr3:58166338
|
A | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.7199-2102A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166338 | ||||||
| chr3:58166381
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.7199-2059A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166381 | ||||||
| chr3:58166563
|
G | A | 1 | a0003c0054t0013g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7199-1877G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166563 | ||||||
| chr3:58166682
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7199-1758C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166682 | ||||||
| chr3:58166820
|
T | TA | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.7199-1609dupA | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr3 | 58166820 | |||||
| chr3:58166828
|
A | AT | 4 | a0002c0036t0009g0075a0003c0009t0004g0009a0003c0009t0004g0017others(1): Show | 4 | HG02040.hp1 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.7199-1612_7199-161 others(5): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166828 | ||||||
| chr3:58166830
|
A | T | 4 | a0002c0036t0009g0075a0003c0009t0004g0009a0003c0009t0004g0017others(1): Show | 4 | HG02040.hp1 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.7199-1610A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166830 | ||||||
| chr3:58166832
|
T | A | 11 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.7199-1608T>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166832 | ||||||
| chr3:58166848
|
G | A | 10 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0007g0127others(7): Show | 10 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.7199-1592G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58166848 | ||||||
| chr3:58167018
|
A | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.7199-1422A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167018 | ||||||
| chr3:58167042
|
C | T | 1 | a0012c0055t0001g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7199-1398C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167042 | ||||||
| chr3:58167072
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.7199-1368A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167072 | ||||||
| chr3:58167073
|
A | G | 1 | a0006c0049t0002g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7199-1367A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167073 | ||||||
| chr3:58167123
|
A | C | 11 | a0001c0030t0003g0128a0004c0006t0002g0048a0004c0006t0002g0050others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.7199-1317A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167123 | ||||||
| chr3:58167125
|
C | G | 2 | a0002c0008t0002g0022a0002c0008t0002g0155 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.7199-1315C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167125 | ||||||
| chr3:58167216
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.7199-1224C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167216 | ||||||
| chr3:58167310
|
T | TTGG | 11 | a0002c0015t0003g0025a0002c0020t0003g0123a0003c0035t0003g0060others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.7199-1129_7199-112 others(7): Show |
FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | INFO_REALIGN_3_PRIME | chr3 | 58167310 | |||||
| chr3:58167605
|
G | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7199-835G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167605 | ||||||
| chr3:58167759
|
G | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0099 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.7199-681G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58167759 | ||||||
| chr3:58168072
|
C | T | 10 | a0002c0002t0001g0176a0002c0003t0001g0134a0002c0003t0007g0127others(7): Show | 10 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.7199-368C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58168072 | ||||||
| chr3:58168077
|
C | G | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7199-363C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58168077 | ||||||
| chr3:58168157
|
A | C | 4 | a0001c0031t0005g0145a0005c0048t0005g0001a0006c0017t0006g0024others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.7199-283A>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58168157 | ||||||
| chr3:58168241
|
G | A | 11 | a0001c0030t0003g0128a0004c0006t0002g0048a0004c0006t0002g0050others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.7199-199G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 43/45 | chr3 | 58168241 | ||||||
| chr3:58168687
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0040 | 2 | HG03927.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.7417+29C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58168687 | ||||||
| chr3:58168746
|
T | C | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7417+88T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58168746 | ||||||
| chr3:58168828
|
G | A | 3 | a0003c0009t0004g0009a0003c0009t0004g0017a0003c0009t0004g0026 | 3 | HG02280.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.7417+170G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58168828 | ||||||
| chr3:58168863
|
C | G | 27 | a0001c0030t0003g0128a0002c0002t0001g0176a0002c0003t0001g0134others(24): Show | 27 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.7417+205C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58168863 | ||||||
| chr3:58168944
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 130 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.7417+286T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58168944 | ||||||
| chr3:58169132
|
G | C | 16 | a0001c0031t0005g0145a0002c0002t0001g0176a0002c0003t0001g0134others(13): Show | 16 | HG00438.hp2 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.7418-458G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58169132 | ||||||
| chr3:58169237
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.7418-353A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58169237 | ||||||
| chr3:58169318
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7418-272G>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58169318 | ||||||
| chr3:58169503
|
C | G | 36 | a0001c0001t0001g0014a0001c0001t0001g0146a0002c0002t0001g0176others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.7418-87C>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 44/45 | chr3 | 58169503 | ||||||
| chr3:58169835
|
C | T | 6 | a0002c0003t0002g0052a0002c0003t0002g0133a0002c0003t0002g0138others(3): Show | 6 | HG00099.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.7621+42C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58169835 | ||||||
| chr3:58170024
|
G | T | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7621+231G>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170024 | ||||||
| chr3:58170057
|
G | A | 2 | a0001c0031t0005g0145a0005c0048t0005g0001 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7621+264G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170057 | ||||||
| chr3:58170144
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7621+351T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170144 | ||||||
| chr3:58170224
|
C | T | 1 | a0003c0009t0004g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7622-351C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170224 | ||||||
| chr3:58170300
|
T | C | 12 | a0001c0001t0004g0144a0002c0008t0014g0110a0002c0036t0009g0075others(9): Show | 12 | HG02040.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.7622-275T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170300 | ||||||
| chr3:58170318
|
T | C | 1 | a0002c0002t0002g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.7622-257T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170318 | ||||||
| chr3:58170327
|
A | T | 1 | a0013c0022t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7622-248A>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170327 | ||||||
| chr3:58170407
|
C | T | 3 | a0001c0030t0003g0128a0001c0031t0005g0145a0005c0048t0005g0001 | 3 | HG02559.hp1 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7622-168C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170407 | ||||||
| chr3:58170424
|
A | G | 1 | a0002c0036t0009g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7622-151A>G | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170424 | ||||||
| chr3:58170449
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.7622-126G>A | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170449 | ||||||
| chr3:58170483
|
T | C | 25 | a0001c0001t0003g0089a0001c0001t0004g0144a0001c0030t0003g0128others(22): Show | 25 | HG01109.hp1 HG01891.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.7622-92T>C | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170483 | ||||||
| chr3:58170515
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.7622-60C>T | FLNB | ENSG00000136068.16 | transcript | ENST00000295956.9 | protein_coding | 45/45 | chr3 | 58170515 |