Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9727 |
|---|---|
| ensemblid | ENSG00000090565.17 |
| hgncid | 17224 |
| symbol | RAB11FIP3 |
| name | RAB11 family interacting protein 3 |
| refseq_nuc | NM_014700.4 |
| refseq_prot | NP_055515.1 |
| ensembl_nuc | ENST00000262305.9 |
| ensembl_prot | ENSP00000262305.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 425649 |
| end | 523011 |
| strand | + |
| ver | v1.2 |
| region | chr16:425649-523011 |
| region5000 | chr16:420649-528011 |
| regionname0 | RAB11FIP3_chr16_425649_523011 |
| regionname5000 | RAB11FIP3_chr16_420649_528011 |
| 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 | 0/1 | 756 | 274 | 75 | 50 | 113 | 11 | 24 | 80 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002 | 0/0 | 756 | 11 | 3 | 0 | 8 | 0 | 0 | 8 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0003 | 0/0 | 756 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0004 | 0/0 | 756 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0005 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0006 | 0/0 | 756 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0007 | 0/0 | 756 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0008 | 0/0 | 756 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0009 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| 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 | 2271 | 219 | 57 | 36 | 101 | 5 | 20 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0002 | 0/1 | 2271 | 41 | 13 | 14 | 4 | 6 | 3 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0003 | 0/0 | 2271 | 10 | 3 | 0 | 7 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0004 | 0/0 | 2271 | 6 | 0 | 0 | 6 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0005 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0006 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0007 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0008 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0009 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0010 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0011 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0012 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0013 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0014 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0015 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0016 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0017 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0018 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| c0019 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| 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 | 2556 | 64 | 9 | 16 | 31 | 3 | 5 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0002 | 0/1 | 2530 | 36 | 5 | 12 | 9 | 4 | 5 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0003 | 0/0 | 2560 | 23 | 1 | 0 | 21 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0004 | 0/0 | 2554 | 12 | 0 | 0 | 12 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0005 | 0/0 | 2532 | 11 | 1 | 2 | 5 | 2 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0006 | 0/0 | 2554 | 11 | 1 | 2 | 4 | 0 | 4 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0007 | 0/0 | 2562 | 10 | 1 | 0 | 9 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0008 | 0/0 | 2556 | 10 | 2 | 1 | 6 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0009 | 0/0 | 2550 | 10 | 5 | 1 | 4 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0010 | 0/0 | 2558 | 10 | 3 | 0 | 2 | 0 | 5 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0011 | 0/0 | 2558 | 9 | 6 | 0 | 3 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0012 | 0/0 | 2560 | 8 | 3 | 3 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0013 | 0/0 | 2574 | 6 | 6 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0014 | 0/0 | 2528 | 6 | 4 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0015 | 0/0 | 2558 | 6 | 6 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0016 | 0/0 | 2534 | 4 | 0 | 0 | 2 | 2 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0017 | 0/0 | 2530 | 4 | 0 | 4 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0018 | 0/0 | 2530 | 3 | 3 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0019 | 0/0 | 2552 | 3 | 2 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0020 | 0/0 | 2576 | 3 | 0 | 2 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0021 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0022 | 0/0 | 2552 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0023 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0024 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0025 | 0/0 | 2572 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0026 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0027 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0028 | 0/0 | 2554 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0029 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0030 | 0/0 | 2530 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0031 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0032 | 0/0 | 2578 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0033 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0034 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0035 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0036 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0037 | 0/0 | 2554 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0038 | 0/0 | 2548 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0039 | 0/0 | 2548 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0040 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0041 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0042 | 0/0 | 2558 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0043 | 0/0 | 2554 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0044 | 0/0 | 2550 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0045 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0046 | 0/0 | 2572 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0047 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0048 | 0/0 | 2572 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0049 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0050 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0051 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0052 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0053 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0054 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0055 | 0/0 | 2532 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0056 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0057 | 0/0 | 2572 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0058 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0059 | 0/0 | 2558 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0060 | 0/0 | 2558 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| t0061 | 0/0 | 2560 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| 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 | 2271 | 219 | 57 | 36 | 101 | 5 | 20 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002 | 0/1 | 2271 | 41 | 13 | 14 | 4 | 6 | 3 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0004 | 0/0 | 2271 | 6 | 0 | 0 | 6 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0006 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0008 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0011 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0012 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0013 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0014 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0019 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003 | 0/0 | 2271 | 10 | 3 | 0 | 7 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0018 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0003c0005 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0004c0007 | 0/0 | 2271 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0005c0017 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0006c0010 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0007c0015 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0008c0016 | 0/0 | 2271 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0009c0009 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4826 | 64 | 9 | 16 | 31 | 3 | 5 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0002 | 0/0 | 4800 | 12 | 2 | 2 | 4 | 1 | 3 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0003 | 0/0 | 4830 | 18 | 1 | 0 | 16 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0004 | 0/0 | 4824 | 12 | 0 | 0 | 12 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0005 | 0/0 | 4802 | 5 | 1 | 1 | 3 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0006 | 0/0 | 4824 | 11 | 1 | 2 | 4 | 0 | 4 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0007 | 0/0 | 4832 | 8 | 1 | 0 | 7 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0008 | 0/0 | 4826 | 9 | 2 | 1 | 5 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0010 | 0/0 | 4828 | 10 | 3 | 0 | 2 | 0 | 5 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0011 | 0/0 | 4828 | 7 | 5 | 0 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0012 | 0/0 | 4830 | 8 | 3 | 3 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0013 | 0/0 | 4844 | 6 | 6 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0014 | 0/0 | 4798 | 3 | 1 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0015 | 0/0 | 4828 | 6 | 6 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0016 | 0/0 | 4804 | 2 | 0 | 0 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0017 | 0/0 | 4800 | 4 | 0 | 4 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0018 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0020 | 0/0 | 4846 | 2 | 0 | 1 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0021 | 0/0 | 4846 | 2 | 0 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0023 | 0/0 | 4832 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0024 | 0/0 | 4826 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0025 | 0/0 | 4842 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0027 | 0/0 | 4805 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0028 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0029 | 0/0 | 4832 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0031 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0033 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0034 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0035 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0036 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0040 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0041 | 0/0 | 4836 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0042 | 0/0 | 4828 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0045 | 0/0 | 4844 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0046 | 0/0 | 4842 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0047 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0048 | 0/0 | 4842 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0049 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0050 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0051 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0055 | 0/0 | 4802 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0056 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0060 | 0/0 | 4828 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0001t0061 | 0/0 | 4830 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0002 | 0/1 | 4800 | 17 | 2 | 9 | 0 | 3 | 2 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0005 | 0/0 | 4802 | 3 | 0 | 1 | 0 | 1 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0009 | 0/0 | 4820 | 9 | 5 | 1 | 3 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0016 | 0/0 | 4804 | 2 | 0 | 0 | 0 | 2 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0019 | 0/0 | 4822 | 3 | 2 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0026 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0030 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0038 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0043 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0044 | 0/0 | 4820 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0053 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0002t0054 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0004t0003 | 0/0 | 4830 | 4 | 0 | 0 | 4 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0004t0008 | 0/0 | 4826 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0004t0011 | 0/0 | 4828 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0006t0032 | 0/0 | 4848 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0006t0058 | 0/0 | 4844 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0008t0057 | 0/0 | 4842 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0011t0002 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0012t0059 | 0/0 | 4828 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0013t0052 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0014t0039 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0001c0019t0002 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003t0002 | 0/0 | 4800 | 4 | 1 | 0 | 3 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003t0005 | 0/0 | 4802 | 2 | 0 | 0 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003t0007 | 0/0 | 4832 | 2 | 0 | 0 | 2 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003t0011 | 0/0 | 4828 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0003t0018 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0002c0018t0009 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0003c0005t0014 | 0/0 | 4798 | 3 | 3 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0004c0007t0022 | 0/0 | 4822 | 2 | 2 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0005c0017t0037 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0006c0010t0005 | 0/0 | 4802 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0007c0015t0020 | 0/0 | 4846 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0008c0016t0002 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| a0009c0009t0003 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | copy fasta | chr16 | 420649 | 528011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0014g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0014g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0016g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0017g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0017g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0017g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0017g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0020g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0020g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0021g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0023g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0023g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0024g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0025g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0025g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0027g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0028g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0029g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0031g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0033g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0034g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0035g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0036g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0040g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0041g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0042g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0045g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0046g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0047g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0048g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0049g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0050g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0051g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0055g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0056g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0060g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0001t0061g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0016g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0019g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0019g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0019g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0026g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0030g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0038g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0043g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0044g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0053g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0002t0054g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0004t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0006t0032g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0006t0058g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0008t0057g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0011t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0012t0059g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0013t0052g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0014t0039g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0001c0019t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0003t0018g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0002c0018t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0003c0005t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0003c0005t0014g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0003c0005t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0004c0007t0022g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0004c0007t0022g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0005c0017t0037g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0006c0010t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0007c0015t0020g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0008c0016t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| a0009c0009t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0169 | EUR | GBR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | GBR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0264 | EUR | GBR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0255 | EUR | GBR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00280 | hp1 | a0001 | c0001 | t0061 | g0241 | EUR | FIN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00280 | hp2 | a0001 | c0002 | t0016 | g0155 | EUR | FIN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0079 | EUR | FIN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00323 | hp2 | a0006 | c0010 | t0005 | g0080 | EUR | FIN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00408 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0233 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00423 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00438 | hp1 | a0001 | c0001 | t0020 | g0236 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0053 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0191 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0247 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00735 | hp2 | a0001 | c0001 | t0012 | g0226 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0142 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01069 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0148 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01071 | hp2 | a0001 | c0001 | t0021 | g0001 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01074 | hp1 | a0001 | c0001 | t0012 | g0280 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0189 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01106 | hp1 | a0001 | c0002 | t0019 | g0285 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01109 | hp2 | a0001 | c0001 | t0042 | g0085 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01167 | hp1 | a0007 | c0015 | t0020 | g0199 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01175 | hp1 | a0001 | c0001 | t0014 | g0143 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01243 | hp1 | a0001 | c0002 | t0038 | g0038 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01258 | hp2 | a0001 | c0002 | t0005 | g0075 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0250 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01261 | hp2 | a0001 | c0002 | t0009 | g0254 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01346 | hp1 | a0001 | c0002 | t0030 | g0147 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0249 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0243 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0141 | EUR | IBS | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01891 | hp2 | a0001 | c0001 | t0024 | g0185 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01928 | hp2 | a0001 | c0001 | t0017 | g0057 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01952 | hp1 | a0001 | c0001 | t0055 | g0058 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01975 | hp2 | a0001 | c0001 | t0017 | g0049 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01978 | hp1 | a0001 | c0001 | t0017 | g0061 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01978 | hp2 | a0008 | c0016 | t0002 | g0114 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0132 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0184 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0237 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02129 | hp1 | a0009 | c0009 | t0003 | g0130 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0207 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02135 | hp1 | a0001 | c0004 | t0003 | g0150 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02135 | hp2 | a0001 | c0004 | t0003 | g0052 | EAS | KHV | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0030 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02145 | hp2 | a0001 | c0002 | t0009 | g0081 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | CDX | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02257 | hp2 | a0001 | c0008 | t0057 | g0113 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02273 | hp2 | a0001 | c0001 | t0017 | g0087 | AMR | PEL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02280 | hp2 | a0001 | c0002 | t0019 | g0037 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02572 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0177 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0129 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02622 | hp1 | a0001 | c0013 | t0052 | g0069 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0269 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0127 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0104 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0044 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0103 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02683 | hp1 | a0001 | c0001 | t0010 | g0195 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0194 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02717 | hp1 | a0005 | c0017 | t0037 | g0100 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0256 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02723 | hp1 | a0004 | c0007 | t0022 | g0067 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02723 | hp2 | a0001 | c0002 | t0044 | g0042 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0188 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0122 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0029 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0033 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02965 | hp1 | a0001 | c0002 | t0054 | g0267 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02970 | hp1 | a0001 | c0001 | t0033 | g0128 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0084 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02976 | hp2 | a0001 | c0001 | t0060 | g0108 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03041 | hp1 | a0001 | c0006 | t0058 | g0111 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03041 | hp2 | a0004 | c0007 | t0022 | g0186 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03098 | hp1 | a0001 | c0001 | t0041 | g0126 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03098 | hp2 | a0001 | c0002 | t0053 | g0271 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0046 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03195 | hp1 | a0001 | c0001 | t0031 | g0166 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0039 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03209 | hp1 | a0001 | c0001 | t0056 | g0124 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03209 | hp2 | a0001 | c0001 | t0023 | g0036 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03239 | hp2 | a0001 | c0001 | t0010 | g0217 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03453 | hp1 | a0003 | c0005 | t0014 | g0023 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03453 | hp2 | a0002 | c0003 | t0002 | g0293 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03486 | hp1 | a0003 | c0005 | t0014 | g0024 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0123 | AFR | ESN | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0258 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03579 | hp1 | a0001 | c0012 | t0059 | g0107 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03579 | hp2 | a0001 | c0006 | t0032 | g0270 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03654 | hp2 | a0001 | c0014 | t0039 | g0112 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03669 | hp1 | a0001 | c0001 | t0029 | g0020 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0273 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0151 | SAS | STU | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0070 | SAS | PJL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | BEB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0244 | SAS | BEB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG04199 | hp2 | a0001 | c0001 | t0010 | g0222 | SAS | STU | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0040 | AFR | YRI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18612 | hp2 | a0001 | c0001 | t0028 | g0091 | EAS | CHB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18942 | hp1 | a0001 | c0001 | t0048 | g0050 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18943 | hp2 | a0001 | c0001 | t0045 | g0138 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18947 | hp1 | a0002 | c0003 | t0002 | g0093 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18947 | hp2 | a0001 | c0002 | t0009 | g0275 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18948 | hp1 | a0002 | c0003 | t0007 | g0095 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18949 | hp1 | a0001 | c0019 | t0002 | g0012 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18950 | hp1 | a0001 | c0011 | t0002 | g0019 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18957 | hp2 | a0001 | c0001 | t0050 | g0168 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18967 | hp2 | a0001 | c0001 | t0008 | g0068 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18975 | hp1 | a0001 | c0002 | t0009 | g0274 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18977 | hp2 | a0002 | c0003 | t0002 | g0094 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18979 | hp2 | a0001 | c0004 | t0011 | g0062 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18982 | hp1 | a0002 | c0003 | t0005 | g0099 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18984 | hp1 | a0001 | c0001 | t0027 | g0163 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18994 | hp2 | a0001 | c0001 | t0012 | g0276 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19000 | hp1 | a0002 | c0003 | t0002 | g0097 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19004 | hp1 | a0001 | c0001 | t0046 | g0131 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19004 | hp2 | a0001 | c0001 | t0051 | g0064 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19007 | hp2 | a0001 | c0001 | t0049 | g0219 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19011 | hp1 | a0001 | c0001 | t0047 | g0139 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19012 | hp2 | a0001 | c0001 | t0011 | g0179 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19030 | hp1 | a0001 | c0001 | t0036 | g0034 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19030 | hp2 | a0002 | c0003 | t0011 | g0102 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0021 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19068 | hp1 | a0001 | c0004 | t0003 | g0175 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19068 | hp2 | a0002 | c0003 | t0005 | g0098 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19074 | hp2 | a0001 | c0001 | t0012 | g0282 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19077 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19077 | hp2 | a0001 | c0002 | t0026 | g0170 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19080 | hp2 | a0002 | c0003 | t0007 | g0096 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19082 | hp1 | a0001 | c0004 | t0003 | g0116 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19082 | hp2 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19087 | hp1 | a0001 | c0004 | t0008 | g0172 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19087 | hp2 | a0002 | c0018 | t0009 | g0092 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19090 | hp2 | a0001 | c0001 | t0034 | g0208 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19240 | hp1 | a0001 | c0001 | t0040 | g0083 | AFR | YRI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA19240 | hp2 | a0001 | c0002 | t0009 | g0253 | AFR | YRI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ASW | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20129 | hp2 | a0001 | c0001 | t0035 | g0045 | AFR | ASW | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20805 | hp1 | a0001 | c0002 | t0016 | g0156 | EUR | TSI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | GIH | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | GIH | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02109 | hp1 | a0002 | c0003 | t0018 | g0101 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02109 | hp2 | a0001 | c0002 | t0019 | g0106 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | ACB | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03471 | hp1 | a0003 | c0005 | t0014 | g0022 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0257 | AFR | MSL | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG06807 | hp1 | a0001 | c0002 | t0009 | g0041 | AFR | USA | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | USA | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18955 | hp1 | a0001 | c0002 | t0009 | g0284 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20300 | hp1 | a0001 | c0001 | t0025 | g0109 | AFR | USA | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | USA | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| NA21309 | hp2 | a0001 | c0002 | t0043 | g0025 | AFR | LWK | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0153 | REF | REF | RAB11FIP3_chr16_420649_528011 | RAB11FIP3 | chr16 | 420649 | 528011 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:426430
|
C | G | 2 | a0002a0005 | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
missense_variant | MODERATE | c.424C>G | p.Pro142Ala | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 782/4801 | 424/2271 | 142/756 | chr16 | 426430 | ||
| chr16:461421
|
G | C | 1 | a0009 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.732G>C | p.Lys244Asn | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/14 | 1090/4801 | 732/2271 | 244/756 | chr16 | 461421 | ||
| chr16:461436
|
T | G | 1 | a0006 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.747T>G | p.Ser249Arg | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/14 | 1105/4801 | 747/2271 | 249/756 | chr16 | 461436 | ||
| chr16:471370
|
A | G | 1 | a0008 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.884A>G | p.Asp295Gly | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/14 | 1242/4801 | 884/2271 | 295/756 | chr16 | 471370 | ||
| chr16:482529
|
A | G | 1 | a0007 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.908A>G | p.Asn303Ser | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/14 | 1266/4801 | 908/2271 | 303/756 | chr16 | 482529 | ||
| chr16:482705
|
G | A | 1 | a0003 | 3 | HG03453.hp1 HG03471.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1084G>A | p.Asp362Asn | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/14 | 1442/4801 | 1084/2271 | 362/756 | chr16 | 482705 | ||
| chr16:520466
|
G | A | 2 | a0004a0005 | 3 | HG02717.hp1 HG02723.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.2024G>A | p.Arg675His | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 13/14 | 2382/4801 | 2024/2271 | 675/756 | chr16 | 520466 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:426096
|
A | G | 19 | a0001c0001a0001c0002a0001c0004others(16): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
synonymous_variant | LOW | c.90A>G | p.Ala30Ala | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 448/4801 | 90/2271 | 30/756 | chr16 | 426096 | ||
| chr16:426120
|
G | A | 2 | a0001c0006a0001c0008 | 3 | HG02257.hp2 HG03041.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.114G>A | p.Glu38Glu | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 472/4801 | 114/2271 | 38/756 | chr16 | 426120 | ||
| chr16:426186
|
C | G | 1 | a0001c0019 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.180C>G | p.Pro60Pro | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 538/4801 | 180/2271 | 60/756 | chr16 | 426186 | ||
| chr16:426561
|
G | C | 1 | a0001c0008 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.555G>C | p.Ser185Ser | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 913/4801 | 555/2271 | 185/756 | chr16 | 426561 | ||
| chr16:471365
|
G | A | 1 | a0001c0011 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.879G>A | p.Glu293Glu | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/14 | 1237/4801 | 879/2271 | 293/756 | chr16 | 471365 | ||
| chr16:488893
|
C | T | 1 | a0001c0014 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1158C>T | p.Gly386Gly | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/14 | 1516/4801 | 1158/2271 | 386/756 | chr16 | 488893 | ||
| chr16:488938
|
G | A | 1 | a0001c0012 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1203G>A | p.Leu401Leu | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/14 | 1561/4801 | 1203/2271 | 401/756 | chr16 | 488938 | ||
| chr16:519769
|
T | C | 1 | a0001c0013 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1738T>C | p.Leu580Leu | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 11/14 | 2096/4801 | 1738/2271 | 580/756 | chr16 | 519769 | ||
| chr16:520557
|
T | C | 15 | a0001c0001a0001c0004a0001c0006others(12): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
synonymous_variant | LOW | c.2115T>C | p.Ser705Ser | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 13/14 | 2473/4801 | 2115/2271 | 705/756 | chr16 | 520557 | ||
| chr16:520791
|
C | A | 2 | a0001c0004a0009c0009 | 7 | HG02129.hp1 HG02135.hp1 HG02135.hp2 others(4): Show |
synonymous_variant | LOW | c.2223C>A | p.Ile741Ile | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 2581/4801 | 2223/2271 | 741/756 | chr16 | 520791 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:425655
|
C | T | 1 | a0001c0001t0061 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-352C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 352 | chr16 | 425655 | |||||
| chr16:425692
|
TCCGGCCT others(16): Show |
T | 2 | a0001c0001t0027a0001c0002t0026 | 2 | NA18984.hp1 NA19077.hp2 |
5_prime_UTR_variant | MODIFIER | c.-288_-266delGCCTCC others(17): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 266 | INFO_REALIGN_3_PRIME | chr16 | 425692 | ||||
| chr16:425717
|
C | G | 3 | a0001c0001t0025a0001c0001t0060a0001c0012t0059 | 4 | HG02976.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-290C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 290 | chr16 | 425717 | |||||
| chr16:425751
|
G | A | 1 | a0001c0001t0028 | 1 | NA18612.hp2 | 5_prime_UTR_variant | MODIFIER | c.-256G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 256 | chr16 | 425751 | |||||
| chr16:425952
|
C | T | 2 | a0001c0006t0058a0001c0008t0057 | 2 | HG02257.hp2 HG03041.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | chr16 | 425952 | ||||||
| chr16:425980
|
CT | C | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
5_prime_UTR_variant | MODIFIER | c.-25delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/14 | 25 | INFO_REALIGN_3_PRIME | chr16 | 425980 | ||||
| chr16:521313
|
C | T | 4 | a0001c0001t0015a0001c0001t0024a0001c0001t0056others(1): Show | 10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*474C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 474 | chr16 | 521313 | |||||
| chr16:521334
|
G | A | 1 | a0001c0001t0029 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 495 | chr16 | 521334 | |||||
| chr16:521353
|
T | C | 1 | a0001c0002t0030 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 514 | chr16 | 521353 | |||||
| chr16:521447
|
C | T | 2 | a0001c0001t0017a0001c0001t0055 | 5 | HG01928.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*608C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 608 | chr16 | 521447 | |||||
| chr16:521470
|
C | T | 2 | a0001c0002t0053a0001c0002t0054 | 2 | HG02965.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*631C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 631 | chr16 | 521470 | |||||
| chr16:521551
|
G | A | 1 | a0001c0008t0057 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 712 | chr16 | 521551 | |||||
| chr16:521730
|
C | T | 1 | a0001c0013t0052 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*891C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 891 | chr16 | 521730 | |||||
| chr16:521731
|
G | A | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 892 | chr16 | 521731 | |||||
| chr16:521746
|
A | C | 1 | a0001c0001t0051 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 907 | chr16 | 521746 | |||||
| chr16:521748
|
A | C | 1 | a0001c0001t0051 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 909 | chr16 | 521748 | |||||
| chr16:521770
|
G | GCCCCCCC others(53): Show |
1 | a0001c0001t0051 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*933_*934insCCCCCC others(54): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 934 | INFO_REALIGN_3_PRIME | chr16 | 521770 | ||||
| chr16:521822
|
G | A | 7 | a0001c0001t0013a0001c0001t0021a0001c0001t0025others(4): Show | 14 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*983G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 983 | chr16 | 521822 | |||||
| chr16:521867
|
G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1028G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1028 | chr16 | 521867 | |||||
| chr16:521904
|
T | C | 50 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(47): Show | 128 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1065T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1065 | chr16 | 521904 | |||||
| chr16:521954
|
G | A | 1 | a0001c0012t0059 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1115G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1115 | chr16 | 521954 | |||||
| chr16:522022
|
T | TGCGTGTG others(5): Show |
1 | a0001c0001t0034 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1190_*1191insCGCG others(8): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1191 | INFO_REALIGN_3_PRIME | chr16 | 522022 | ||||
| chr16:522032
|
T | C | 3 | a0001c0001t0025a0001c0008t0057a0001c0012t0059 | 4 | HG02257.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1193T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1193 | chr16 | 522032 | |||||
| chr16:522038
|
C | CATGTGTG others(3): Show |
1 | a0001c0001t0034 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199_*1200insATGT others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1200 | chr16 | 522038 | |||||
| chr16:522038
|
C | CGTGTGTG others(17): Show |
1 | a0001c0012t0059 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200_*1201insTGTG others(20): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1201 | INFO_REALIGN_3_PRIME | chr16 | 522038 | ||||
| chr16:522038
|
C | CGTGTGTG others(33): Show |
2 | a0001c0001t0025a0001c0008t0057 | 3 | HG02257.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1200_*1201insTGTG others(36): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1201 | INFO_REALIGN_3_PRIME | chr16 | 522038 | ||||
| chr16:522044
|
T | C | 9 | a0001c0001t0018a0001c0001t0025a0001c0001t0033others(6): Show | 11 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1205T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1205 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGCGCG others(17): Show |
5 | a0001c0001t0036a0001c0002t0038a0001c0014t0039others(2): Show | 6 | HG01243.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGC others(20): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGCGCG others(33): Show |
1 | a0001c0001t0048 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGC others(36): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(19): Show |
39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 198 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(35): Show |
4 | a0001c0001t0013a0001c0001t0020a0001c0006t0058others(1): Show | 10 | HG00438.hp1 HG00735.hp1 HG01167.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(38): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(37): Show |
1 | a0001c0006t0032 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(40): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(35): Show |
1 | a0001c0001t0021 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(38): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(31): Show |
2 | a0001c0001t0045a0001c0001t0046 | 2 | NA18943.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(34): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522044
|
T | TGTGTGCG others(19): Show |
1 | a0001c0001t0047 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205_*1206insGTGT others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522044 | |||||
| chr16:522045
|
A | G | 2 | a0001c0002t0044a0001c0002t0054 | 2 | HG02723.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1206A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1206 | chr16 | 522045 | |||||
| chr16:522243
|
G | A | 1 | a0001c0001t0040 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1404G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1404 | chr16 | 522243 | |||||
| chr16:522245
|
A | AAT | 19 | a0001c0001t0005a0001c0001t0010a0001c0001t0011others(16): Show | 52 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1433_*1434dupAT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1435 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
A | AATAT | 15 | a0001c0001t0003a0001c0001t0012a0001c0001t0016others(12): Show | 46 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1431_*1434dupATAT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1435 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
A | AATATAT | 6 | a0001c0001t0007a0001c0001t0023a0001c0001t0029others(3): Show | 15 | HG00544.hp1 HG00544.hp2 HG02074.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1429_*1434dupATAT others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1435 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
A | AATATATA others(3): Show |
1 | a0001c0001t0041 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1425_*1434dupATAT others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1435 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
AAT | A | 7 | a0001c0001t0004a0001c0001t0006a0001c0001t0014others(4): Show | 33 | HG00609.hp2 HG00673.hp2 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1433_*1434delAT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1433 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
AATAT | A | 3 | a0001c0002t0019a0001c0002t0053a0001c0002t0054 | 5 | HG01106.hp1 HG02109.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1431_*1434delATAT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1431 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522245
|
AATATAT | A | 6 | a0001c0002t0009a0001c0002t0026a0001c0002t0038others(3): Show | 14 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1429_*1434delATAT others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1429 | INFO_REALIGN_3_PRIME | chr16 | 522245 | ||||
| chr16:522522
|
G | C | 1 | a0001c0008t0057 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1683 | chr16 | 522522 | |||||
| chr16:522626
|
C | G | 1 | a0001c0001t0042 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1787 | chr16 | 522626 | |||||
| chr16:522788
|
G | C | 9 | a0001c0002t0009a0001c0002t0019a0001c0002t0026others(6): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1949G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 1949 | chr16 | 522788 | |||||
| chr16:522855
|
G | T | 9 | a0001c0002t0009a0001c0002t0019a0001c0002t0026others(6): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2016G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 2016 | chr16 | 522855 | |||||
| chr16:522870
|
G | A | 3 | a0001c0001t0018a0001c0001t0033a0002c0003t0018 | 4 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2031G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 2031 | chr16 | 522870 | |||||
| chr16:522882
|
G | A | 1 | a0001c0001t0049 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2043G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 2043 | chr16 | 522882 | |||||
| chr16:522893
|
C | T | 1 | a0001c0001t0050 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 14/14 | 2054 | chr16 | 522893 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:426796
|
C | A | 11 | a0001c0001t0001g0006a0001c0001t0002g0002a0001c0001t0002g0005others(8): Show | 11 | HG00408.hp1 HG00423.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+76C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 426796 | ||||||
| chr16:426905
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+185C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 426905 | ||||||
| chr16:426906
|
C | T | 1 | a0002c0003t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.714+186C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 426906 | ||||||
| chr16:427058
|
G | C | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+338G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427058 | ||||||
| chr16:427145
|
G | A | 8 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0004g0018others(5): Show | 8 | HG03669.hp1 NA18950.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+425G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427145 | ||||||
| chr16:427205
|
A | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+485A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427205 | ||||||
| chr16:427215
|
C | T | 1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.714+495C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427215 | ||||||
| chr16:427242
|
T | C | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.714+522T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427242 | ||||||
| chr16:427253
|
T | C | 1 | a0002c0003t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.714+533T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427253 | ||||||
| chr16:427407
|
A | G | 111 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.714+687A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427407 | ||||||
| chr16:427619
|
C | G | 111 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.714+899C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427619 | ||||||
| chr16:427626
|
A | T | 1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.714+906A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427626 | ||||||
| chr16:427627
|
T | A | 1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.714+907T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427627 | ||||||
| chr16:427747
|
G | A | 25 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(22): Show | 25 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.714+1027G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427747 | ||||||
| chr16:427812
|
C | G | 1 | a0001c0001t0001g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.714+1092C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 427812 | ||||||
| chr16:428018
|
G | A | 2 | a0001c0001t0007g0047a0001c0001t0007g0048 | 2 | HG00544.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.714+1298G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428018 | ||||||
| chr16:428100
|
C | CA | 108 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0001g0197others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.714+1392dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 428100 | |||||
| chr16:428100
|
C | CAA | 40 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0005g0105others(37): Show | 41 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.714+1391_714+1392d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 428100 | |||||
| chr16:428100
|
C | CAAA | 59 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.714+1390_714+1392d others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 428100 | |||||
| chr16:428200
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00438.hp2 HG00597.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1480G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428200 | ||||||
| chr16:428270
|
A | G | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+1550A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428270 | ||||||
| chr16:428405
|
G | C | 1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.714+1685G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428405 | ||||||
| chr16:428449
|
C | G | 4 | a0001c0001t0004g0088a0001c0001t0004g0089a0001c0001t0004g0090others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1729C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428449 | ||||||
| chr16:428503
|
C | G | 1 | a0001c0001t0011g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.714+1783C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428503 | ||||||
| chr16:428514
|
A | G | 4 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0001t0060g0108others(1): Show | 4 | HG02976.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+1794A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428514 | ||||||
| chr16:428574
|
T | A | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+1854T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428574 | ||||||
| chr16:428832
|
T | G | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+2112T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428832 | ||||||
| chr16:428942
|
C | T | 1 | a0001c0001t0017g0087 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.714+2222C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 428942 | ||||||
| chr16:429010
|
A | G | 82 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(79): Show | 82 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.714+2290A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429010 | ||||||
| chr16:429147
|
G | A | 1 | a0001c0001t0010g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+2427G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429147 | ||||||
| chr16:429259
|
A | T | 2 | a0001c0001t0002g0176a0001c0001t0014g0177 | 2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.714+2539A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429259 | ||||||
| chr16:429312
|
G | A | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+2592G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429312 | ||||||
| chr16:429315
|
T | G | 29 | a0001c0001t0003g0060a0001c0001t0004g0051a0001c0001t0004g0054others(26): Show | 29 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.714+2595T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429315 | ||||||
| chr16:429347
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.714+2627C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429347 | ||||||
| chr16:429538
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.714+2818C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429538 | ||||||
| chr16:429592
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+2872C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429592 | ||||||
| chr16:429602
|
C | T | 74 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(71): Show | 74 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.714+2882C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429602 | ||||||
| chr16:429641
|
C | T | 3 | a0002c0003t0011g0102a0002c0003t0018g0101a0005c0017t0037g0100 | 3 | HG02109.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.714+2921C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429641 | ||||||
| chr16:429649
|
G | A | 2 | a0001c0001t0002g0002a0001c0019t0002g0012 | 2 | NA18949.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.714+2929G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429649 | ||||||
| chr16:429857
|
C | G | 3 | a0002c0003t0011g0102a0002c0003t0018g0101a0005c0017t0037g0100 | 3 | HG02109.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.714+3137C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429857 | ||||||
| chr16:429987
|
C | G | 1 | a0001c0001t0012g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.714+3267C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 429987 | ||||||
| chr16:430029
|
AAC | A | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+3313_714+3314d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 430029 | |||||
| chr16:430096
|
T | C | 237 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(234): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.714+3376T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430096 | ||||||
| chr16:430172
|
A | G | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.714+3452A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430172 | ||||||
| chr16:430195
|
C | T | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+3475C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430195 | ||||||
| chr16:430209
|
G | A | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+3489G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430209 | ||||||
| chr16:430342
|
T | A | 1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.714+3622T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430342 | ||||||
| chr16:430542
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.714+3822A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430542 | ||||||
| chr16:430721
|
A | G | 1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.714+4001A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430721 | ||||||
| chr16:430753
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+4033C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430753 | ||||||
| chr16:430791
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+4071A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430791 | ||||||
| chr16:430810
|
C | T | 2 | a0002c0003t0005g0098a0002c0003t0005g0099 | 2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.714+4090C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430810 | ||||||
| chr16:430875
|
A | G | 207 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.714+4155A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430875 | ||||||
| chr16:430921
|
A | C | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(43): Show | 46 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.714+4201A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430921 | ||||||
| chr16:430928
|
C | A | 2 | a0001c0001t0014g0142a0001c0001t0014g0143 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.714+4208C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 430928 | ||||||
| chr16:431015
|
A | G | 1 | a0001c0001t0012g0280 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.714+4295A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431015 | ||||||
| chr16:431186
|
G | A | 1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.714+4466G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431186 | ||||||
| chr16:431211
|
G | T | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | NA18964.hp2 NA18990.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+4491G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431211 | ||||||
| chr16:431253
|
G | C | 108 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.714+4533G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431253 | ||||||
| chr16:431324
|
A | C | 1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.714+4604A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431324 | ||||||
| chr16:431382
|
CT | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0002g0176others(3): Show | 6 | HG01074.hp2 HG02896.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+4677delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 431382 | |||||
| chr16:431398
|
G | T | 2 | a0001c0001t0025g0021a0001c0001t0025g0109 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.714+4678G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431398 | ||||||
| chr16:431524
|
C | T | 1 | a0001c0004t0003g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.714+4804C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431524 | ||||||
| chr16:431539
|
T | G | 1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.714+4819T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431539 | ||||||
| chr16:431553
|
T | G | 120 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.714+4833T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431553 | ||||||
| chr16:431562
|
A | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+4842A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431562 | ||||||
| chr16:431595
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.714+4875G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431595 | ||||||
| chr16:431664
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+4944C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431664 | ||||||
| chr16:431665
|
G | A | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+4945G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431665 | ||||||
| chr16:431754
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0008g0191 | 2 | HG00558.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.714+5034G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431754 | ||||||
| chr16:431759
|
A | T | 1 | a0001c0001t0006g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.714+5039A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431759 | ||||||
| chr16:431759
|
AT | A | 6 | a0001c0001t0002g0176a0001c0001t0015g0122a0001c0001t0017g0049others(3): Show | 6 | HG01256.hp1 HG01346.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.714+5054delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 431759 | |||||
| chr16:431779
|
T | C | 1 | a0001c0002t0005g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.714+5059T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431779 | ||||||
| chr16:431871
|
C | T | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(43): Show | 46 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.714+5151C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431871 | ||||||
| chr16:431881
|
T | C | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(43): Show | 46 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.714+5161T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431881 | ||||||
| chr16:431906
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.714+5186G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431906 | ||||||
| chr16:431917
|
C | T | 1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.714+5197C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 431917 | ||||||
| chr16:432134
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+5414A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432134 | ||||||
| chr16:432153
|
C | T | 1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.714+5433C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432153 | ||||||
| chr16:432173
|
A | T | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+5453A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432173 | ||||||
| chr16:432254
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(171): Show | 174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.714+5534A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432254 | ||||||
| chr16:432277
|
C | T | 294 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.714+5557C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432277 | ||||||
| chr16:432355
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.714+5635C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432355 | ||||||
| chr16:432376
|
G | A | 48 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.714+5656G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432376 | ||||||
| chr16:432557
|
C | T | 1 | a0001c0001t0010g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.714+5837C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432557 | ||||||
| chr16:432572
|
C | T | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+5852C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432572 | ||||||
| chr16:432587
|
G | GT | 39 | a0001c0001t0001g0140a0001c0001t0001g0259a0001c0001t0001g0262others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.714+5883dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 432587 | |||||
| chr16:432602
|
T | G | 2 | a0001c0001t0010g0194a0001c0001t0010g0195 | 2 | HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.714+5882T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432602 | ||||||
| chr16:432603
|
TG | T | 10 | a0001c0001t0004g0051a0001c0001t0011g0256a0001c0001t0011g0257others(7): Show | 10 | HG00140.hp2 HG00673.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+5884delG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432603 | ||||||
| chr16:432604
|
G | T | 188 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(185): Show | 189 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.714+5884G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432604 | ||||||
| chr16:432606
|
G | T | 4 | a0001c0014t0039g0112a0002c0003t0011g0102a0002c0003t0018g0101others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+5886G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432606 | ||||||
| chr16:432750
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.714+6030C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432750 | ||||||
| chr16:432839
|
C | G | 1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.714+6119C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432839 | ||||||
| chr16:432948
|
T | C | 2 | a0001c0001t0007g0053a0001c0004t0003g0052 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.714+6228T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 432948 | ||||||
| chr16:433011
|
G | A | 1 | a0001c0001t0015g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.714+6291G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433011 | ||||||
| chr16:433018
|
C | T | 2 | a0001c0001t0005g0105a0001c0002t0019g0106 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.714+6298C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433018 | ||||||
| chr16:433028
|
C | CT | 9 | a0001c0001t0001g0140a0001c0001t0002g0009a0001c0001t0007g0048others(6): Show | 9 | HG01981.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+6331dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433028 | |||||
| chr16:433028
|
CT | C | 134 | a0001c0001t0001g0115a0001c0001t0001g0182a0001c0001t0001g0193others(131): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.714+6331delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433028 | |||||
| chr16:433028
|
CTT | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0288others(3): Show | 6 | HG01070.hp1 HG01167.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.714+6330_714+6331d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433028 | |||||
| chr16:433079
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+6359G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433079 | ||||||
| chr16:433107
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+6387C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433107 | ||||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
1 | a0001c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
29 | a0001c0001t0008g0294a0001c0001t0010g0032a0001c0001t0010g0046others(26): Show | 29 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
1 | a0001c0004t0003g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0251 | 2 | HG01361.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
2 | a0001c0001t0010g0004a0001c0001t0016g0003 | 2 | HG00423.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(728): Show |
5 | a0001c0001t0001g0259a0001c0001t0001g0283a0001c0002t0009g0274others(2): Show | 5 | HG02738.hp1 HG04199.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(737): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(726): Show |
7 | a0001c0001t0001g0182a0001c0001t0006g0187a0001c0001t0010g0188others(4): Show | 8 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(735): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
190 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
1 | a0001c0006t0032g0270 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(728): Show |
1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.714+6437_714+6438i others(737): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(725): Show |
1 | a0001c0001t0001g0145 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.714+6437_714+6438i others(734): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
4 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0001t0060g0108others(1): Show | 4 | HG02976.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(726): Show |
1 | a0001c0001t0017g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.714+6437_714+6438i others(735): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
45 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433137
|
C | CATTCTCC others(727): Show |
1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.714+6437_714+6438i others(736): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 433137 | |||||
| chr16:433332
|
A | G | 79 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0001g0198others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.714+6612A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433332 | ||||||
| chr16:433420
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.714+6700A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433420 | ||||||
| chr16:433451
|
G | A | 1 | a0001c0001t0002g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.714+6731G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433451 | ||||||
| chr16:433490
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+6770C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433490 | ||||||
| chr16:433664
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+6944C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433664 | ||||||
| chr16:433737
|
A | T | 122 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.714+7017A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433737 | ||||||
| chr16:433773
|
G | A | 2 | a0001c0001t0005g0105a0001c0002t0019g0106 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.714+7053G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433773 | ||||||
| chr16:433774
|
T | G | 1 | a0001c0001t0056g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.714+7054T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433774 | ||||||
| chr16:433810
|
C | A | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.714+7090C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433810 | ||||||
| chr16:433895
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+7175T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 433895 | ||||||
| chr16:434103
|
A | G | 125 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.714+7383A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434103 | ||||||
| chr16:434264
|
A | G | 1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.714+7544A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434264 | ||||||
| chr16:434345
|
C | T | 10 | a0001c0001t0001g0259a0002c0003t0002g0093a0002c0003t0002g0094others(7): Show | 10 | HG02738.hp1 HG03453.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.714+7625C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434345 | ||||||
| chr16:434369
|
G | C | 207 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.714+7649G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434369 | ||||||
| chr16:434403
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+7683C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434403 | ||||||
| chr16:434430
|
A | ATACTTTA others(311): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+7724_714+7725i others(320): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 434430 | |||||
| chr16:434430
|
A | ATACTTTA others(310): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+7724_714+7725i others(319): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 434430 | |||||
| chr16:434434
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0008g0191 | 2 | HG00558.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.714+7714T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434434 | ||||||
| chr16:434589
|
C | A | 76 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(73): Show | 76 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.714+7869C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434589 | ||||||
| chr16:434589
|
C | G | 127 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(124): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.714+7869C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434589 | ||||||
| chr16:434613
|
G | T | 1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.714+7893G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434613 | ||||||
| chr16:434840
|
G | A | 1 | a0001c0001t0006g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.714+8120G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434840 | ||||||
| chr16:434915
|
C | G | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+8195C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 434915 | ||||||
| chr16:435009
|
G | C | 1 | a0001c0001t0004g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.714+8289G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435009 | ||||||
| chr16:435179
|
T | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+8459T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435179 | ||||||
| chr16:435204
|
C | CA | 8 | a0001c0001t0002g0010a0001c0001t0002g0174a0001c0001t0004g0089others(5): Show | 9 | HG00609.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+8501dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 435204 | |||||
| chr16:435204
|
C | CAAAAAAA others(8): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+8487_714+8501d others(17): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 435204 | |||||
| chr16:435204
|
C | CAAAAAAA others(9): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+8486_714+8501d others(18): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 435204 | |||||
| chr16:435260
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+8540A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435260 | ||||||
| chr16:435390
|
A | G | 3 | a0001c0001t0002g0086a0001c0001t0011g0084a0001c0001t0042g0085 | 3 | HG01109.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.714+8670A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435390 | ||||||
| chr16:435520
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+8800A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435520 | ||||||
| chr16:435555
|
T | C | 149 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0001g0197others(146): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.714+8835T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435555 | ||||||
| chr16:435700
|
CTTTGCAC others(2091): Show |
C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+8983_714+11080 others(3): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 435700 | |||||
| chr16:435708
|
A | G | 1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.714+8988A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435708 | ||||||
| chr16:435767
|
T | G | 1 | a0001c0002t0009g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.714+9047T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 435767 | ||||||
| chr16:436099
|
A | G | 1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.714+9379A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436099 | ||||||
| chr16:436223
|
T | C | 197 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.714+9503T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436223 | ||||||
| chr16:436239
|
G | A | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+9519G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436239 | ||||||
| chr16:436258
|
A | G | 1 | a0001c0001t0018g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.714+9538A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436258 | ||||||
| chr16:436265
|
C | T | 1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.714+9545C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436265 | ||||||
| chr16:436268
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.714+9548C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436268 | ||||||
| chr16:436312
|
G | A | 228 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(225): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.714+9592G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436312 | ||||||
| chr16:436317
|
A | C | 6 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+9597A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436317 | ||||||
| chr16:436337
|
A | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+9617A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436337 | ||||||
| chr16:436337
|
A | G | 169 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(166): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.714+9617A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436337 | ||||||
| chr16:436449
|
C | T | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+9729C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436449 | ||||||
| chr16:436465
|
C | CATTT | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+9762_714+9765d others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 436465 | |||||
| chr16:436634
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.714+9914A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436634 | ||||||
| chr16:436750
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+10030A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436750 | ||||||
| chr16:436792
|
C | A | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+10072C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436792 | ||||||
| chr16:436826
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.714+10106C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436826 | ||||||
| chr16:436867
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+10147T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 436867 | ||||||
| chr16:437005
|
G | GTGGCTCA others(336): Show |
1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.714+10299_714+1030 others(347): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437005 | |||||
| chr16:437087
|
A | G | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+10367A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437087 | ||||||
| chr16:437129
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+10409T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437129 | ||||||
| chr16:437132
|
G | T | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0012t0059g0107 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.714+10412G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437132 | ||||||
| chr16:437180
|
A | C | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+10460A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437180 | ||||||
| chr16:437210
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+10490G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437210 | ||||||
| chr16:437224
|
G | C | 71 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.714+10504G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437224 | ||||||
| chr16:437234
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+10514C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437234 | ||||||
| chr16:437334
|
C | T | 5 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+10614C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437334 | ||||||
| chr16:437444
|
C | T | 10 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(7): Show | 10 | HG00140.hp2 HG00735.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.714+10724C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437444 | ||||||
| chr16:437570
|
C | CA | 106 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.714+10872dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437570 | |||||
| chr16:437570
|
C | CAA | 9 | a0001c0001t0003g0125a0001c0001t0013g0035a0001c0001t0014g0177others(6): Show | 9 | HG02135.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.714+10871_714+1087 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437570 | |||||
| chr16:437651
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+10931C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437651 | ||||||
| chr16:437678
|
A | G | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+10958A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437678 | ||||||
| chr16:437728
|
T | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(184): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.714+11008T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437728 | ||||||
| chr16:437795
|
A | T | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+11075A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437795 | ||||||
| chr16:437802
|
T | C | 1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.714+11082T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437802 | ||||||
| chr16:437802
|
TTA | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11084_714+1108 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437802 | |||||
| chr16:437815
|
C | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11095C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437815 | ||||||
| chr16:437816
|
A | G | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11096A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437816 | ||||||
| chr16:437818
|
T | A | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11098T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437818 | ||||||
| chr16:437821
|
C | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11101C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437821 | ||||||
| chr16:437824
|
G | A | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11104G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437824 | ||||||
| chr16:437826
|
T | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11106T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437826 | ||||||
| chr16:437827
|
C | CT | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11108dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437827 | |||||
| chr16:437833
|
C | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11113C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437833 | ||||||
| chr16:437845
|
T | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11125T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437845 | ||||||
| chr16:437856
|
G | T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11136G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437856 | ||||||
| chr16:437861
|
T | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11141T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437861 | ||||||
| chr16:437862
|
G | A | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11142G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 437862 | ||||||
| chr16:437865
|
TCATTCTT others(10): Show |
T | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | NA18942.hp2 NA18964.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+11148_714+1116 others(21): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 437865 | |||||
| chr16:438067
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+11347C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438067 | ||||||
| chr16:438074
|
G | T | 1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.714+11354G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438074 | ||||||
| chr16:438194
|
G | A | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0012t0059g0107 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.714+11474G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438194 | ||||||
| chr16:438319
|
G | A | 42 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.714+11599G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438319 | ||||||
| chr16:438404
|
C | CT | 73 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0120others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.714+11703dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 438404 | |||||
| chr16:438404
|
C | CTT | 7 | a0001c0001t0003g0180a0001c0001t0004g0088a0001c0001t0005g0066others(4): Show | 7 | HG00558.hp1 HG01978.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+11702_714+1170 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 438404 | |||||
| chr16:438470
|
A | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+11750A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438470 | ||||||
| chr16:438554
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+11834C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438554 | ||||||
| chr16:438562
|
C | A | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+11842C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438562 | ||||||
| chr16:438563
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0242 | 3 | HG01175.hp2 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.714+11843G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438563 | ||||||
| chr16:438690
|
A | AT | 142 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0115others(139): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.714+11985dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 438690 | |||||
| chr16:438690
|
A | ATT | 12 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.714+11984_714+1198 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 438690 | |||||
| chr16:438722
|
G | A | 1 | a0001c0001t0006g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.714+12002G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438722 | ||||||
| chr16:438744
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+12024C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438744 | ||||||
| chr16:438776
|
G | A | 5 | a0001c0001t0017g0049a0001c0001t0017g0057a0001c0001t0017g0061others(2): Show | 5 | HG01928.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+12056G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438776 | ||||||
| chr16:438791
|
G | T | 1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.714+12071G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438791 | ||||||
| chr16:438932
|
C | G | 2 | a0001c0001t0060g0108a0001c0012t0059g0107 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.714+12212C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 438932 | ||||||
| chr16:439055
|
C | T | 1 | a0001c0001t0061g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.714+12335C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439055 | ||||||
| chr16:439131
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.714+12411G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439131 | ||||||
| chr16:439193
|
A | G | 2 | a0001c0001t0005g0105a0001c0002t0019g0106 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.714+12473A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439193 | ||||||
| chr16:439212
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+12492A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439212 | ||||||
| chr16:439278
|
C | T | 1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.714+12558C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439278 | ||||||
| chr16:439483
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.714+12763G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439483 | ||||||
| chr16:439580
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+12860A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439580 | ||||||
| chr16:439603
|
A | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.714+12883A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439603 | ||||||
| chr16:439651
|
C | T | 3 | a0002c0003t0011g0102a0002c0003t0018g0101a0005c0017t0037g0100 | 3 | HG02109.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.714+12931C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439651 | ||||||
| chr16:439675
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.714+12955C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439675 | ||||||
| chr16:439875
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+13155C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439875 | ||||||
| chr16:439985
|
A | G | 71 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(68): Show | 71 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.714+13265A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 439985 | ||||||
| chr16:440041
|
T | C | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+13321T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440041 | ||||||
| chr16:440051
|
A | T | 1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.714+13331A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440051 | ||||||
| chr16:440082
|
C | T | 1 | a0001c0001t0028g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.714+13362C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440082 | ||||||
| chr16:440123
|
G | A | 8 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(5): Show | 8 | HG00609.hp1 HG02080.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+13403G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440123 | ||||||
| chr16:440132
|
C | T | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+13412C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440132 | ||||||
| chr16:440141
|
C | A | 2 | a0001c0001t0060g0108a0001c0012t0059g0107 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.714+13421C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440141 | ||||||
| chr16:440219
|
C | T | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.714+13499C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440219 | ||||||
| chr16:440267
|
T | A | 11 | a0001c0001t0001g0266a0001c0001t0020g0247a0001c0002t0002g0183others(8): Show | 11 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+13547T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440267 | ||||||
| chr16:440280
|
T | G | 1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.714+13560T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440280 | ||||||
| chr16:440539
|
C | T | 5 | a0001c0001t0001g0239a0001c0001t0006g0196a0001c0001t0006g0207others(2): Show | 5 | HG01346.hp2 HG02027.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+13819C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440539 | ||||||
| chr16:440612
|
T | C | 2 | a0001c0001t0060g0108a0001c0012t0059g0107 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.714+13892T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440612 | ||||||
| chr16:440645
|
A | G | 187 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(184): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.714+13925A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440645 | ||||||
| chr16:440666
|
A | G | 2 | a0001c0001t0005g0105a0001c0002t0019g0106 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.714+13946A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440666 | ||||||
| chr16:440679
|
G | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+13959G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440679 | ||||||
| chr16:440820
|
G | A | 25 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(22): Show | 25 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.714+14100G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440820 | ||||||
| chr16:440835
|
A | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(164): Show | 167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.714+14115A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440835 | ||||||
| chr16:440874
|
C | G | 1 | a0001c0001t0011g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.714+14154C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 440874 | ||||||
| chr16:441067
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.714+14347A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441067 | ||||||
| chr16:441125
|
T | C | 81 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(78): Show | 81 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.714+14405T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441125 | ||||||
| chr16:441132
|
G | A | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+14412G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441132 | ||||||
| chr16:441188
|
T | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(184): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.714+14468T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441188 | ||||||
| chr16:441199
|
C | CG | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+14480dupG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 441199 | |||||
| chr16:441247
|
A | G | 1 | a0001c0001t0012g0280 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.714+14527A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441247 | ||||||
| chr16:441355
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+14635C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441355 | ||||||
| chr16:441394
|
C | T | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+14674C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441394 | ||||||
| chr16:441405
|
C | T | 45 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.714+14685C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441405 | ||||||
| chr16:441484
|
G | T | 2 | a0001c0002t0009g0081a0006c0010t0005g0080 | 2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.714+14764G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441484 | ||||||
| chr16:441566
|
C | G | 2 | a0001c0001t0004g0055a0001c0001t0004g0056 | 2 | NA18971.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.714+14846C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 441566 | ||||||
| chr16:442307
|
T | C | 1 | a0001c0001t0003g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.714+15587T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442307 | ||||||
| chr16:442333
|
C | G | 1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.714+15613C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442333 | ||||||
| chr16:442368
|
C | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.714+15648C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442368 | ||||||
| chr16:442514
|
G | T | 12 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(9): Show | 12 | HG02109.hp1 HG02717.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.714+15794G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442514 | ||||||
| chr16:442522
|
G | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+15802G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442522 | ||||||
| chr16:442529
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.714+15809C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442529 | ||||||
| chr16:442603
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+15883A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442603 | ||||||
| chr16:442708
|
G | A | 1 | a0001c0001t0011g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.714+15988G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442708 | ||||||
| chr16:442748
|
C | T | 1 | a0001c0001t0007g0237 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.714+16028C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442748 | ||||||
| chr16:442824
|
A | T | 1 | a0001c0004t0003g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.714+16104A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 442824 | ||||||
| chr16:443086
|
A | G | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+16366A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443086 | ||||||
| chr16:443171
|
G | A | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+16451G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443171 | ||||||
| chr16:443272
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.714+16552G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443272 | ||||||
| chr16:443368
|
C | G | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+16648C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443368 | ||||||
| chr16:443407
|
C | G | 1 | a0001c0001t0006g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.714+16687C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443407 | ||||||
| chr16:443408
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.714+16688G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443408 | ||||||
| chr16:443496
|
A | C | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+16776A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443496 | ||||||
| chr16:443574
|
T | G | 5 | a0001c0001t0001g0214a0001c0001t0001g0262a0001c0002t0053g0271others(2): Show | 5 | HG00408.hp2 HG02132.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+16854T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443574 | ||||||
| chr16:443604
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0010g0004a0001c0008t0057g0113others(1): Show | 4 | HG00423.hp2 HG02257.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+16884C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443604 | ||||||
| chr16:443621
|
A | C | 1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.714+16901A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443621 | ||||||
| chr16:443692
|
A | G | 1 | a0001c0002t0030g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.714+16972A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443692 | ||||||
| chr16:443698
|
T | G | 1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.714+16978T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443698 | ||||||
| chr16:443766
|
A | G | 1 | a0002c0003t0002g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.714+17046A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443766 | ||||||
| chr16:443771
|
A | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+17051A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443771 | ||||||
| chr16:443772
|
G | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+17052G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443772 | ||||||
| chr16:443781
|
A | G | 49 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.714+17061A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443781 | ||||||
| chr16:443785
|
A | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+17065A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443785 | ||||||
| chr16:443786
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+17066G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443786 | ||||||
| chr16:443792
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+17072C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443792 | ||||||
| chr16:443800
|
G | C | 1 | a0001c0001t0010g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+17080G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443800 | ||||||
| chr16:443844
|
A | G | 149 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.714+17124A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443844 | ||||||
| chr16:443852
|
T | C | 2 | a0001c0001t0003g0235a0001c0001t0020g0236 | 2 | HG00438.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.714+17132T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443852 | ||||||
| chr16:443903
|
C | T | 1 | a0001c0001t0018g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.714+17183C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443903 | ||||||
| chr16:443995
|
A | G | 2 | a0001c0001t0012g0104a0001c0001t0023g0103 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.714+17275A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 443995 | ||||||
| chr16:444011
|
C | T | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714+17291C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444011 | ||||||
| chr16:444346
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-17058A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444346 | ||||||
| chr16:444353
|
C | T | 1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.715-17051C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444353 | ||||||
| chr16:444402
|
G | C | 3 | a0001c0001t0015g0136a0001c0001t0041g0126a0001c0001t0056g0124 | 3 | HG02572.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.715-17002G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444402 | ||||||
| chr16:444411
|
A | G | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-16993A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444411 | ||||||
| chr16:444538
|
T | C | 2 | a0001c0002t0002g0146a0001c0002t0002g0152 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.715-16866T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444538 | ||||||
| chr16:444750
|
C | G | 1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-16654C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444750 | ||||||
| chr16:444893
|
A | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-16511A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444893 | ||||||
| chr16:444894
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-16510T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444894 | ||||||
| chr16:444910
|
C | T | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.715-16494C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444910 | ||||||
| chr16:444929
|
A | G | 81 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(78): Show | 81 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.715-16475A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444929 | ||||||
| chr16:444986
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.715-16418T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 444986 | ||||||
| chr16:445113
|
C | CA | 96 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0118others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.715-16273dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445113 | |||||
| chr16:445113
|
C | CAA | 7 | a0001c0001t0001g0117a0001c0001t0002g0002a0001c0001t0015g0136others(4): Show | 7 | HG00438.hp2 HG01106.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-16274_715-1627 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445113 | |||||
| chr16:445113
|
C | CAAA | 32 | a0001c0001t0005g0105a0001c0001t0008g0294a0001c0001t0010g0032others(29): Show | 32 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-16275_715-1627 others(7): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445113 | |||||
| chr16:445113
|
C | CAAAA | 45 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.715-16276_715-1627 others(8): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445113 | |||||
| chr16:445124
|
AAAAAAAA others(325): Show |
A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-16270_715-1593 others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445124 | |||||
| chr16:445132
|
G | A | 1 | a0001c0001t0023g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.715-16272G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445132 | ||||||
| chr16:445278
|
C | CA | 67 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.715-16115dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 445278 | |||||
| chr16:445331
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.715-16073T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445331 | ||||||
| chr16:445353
|
C | T | 1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-16051C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445353 | ||||||
| chr16:445405
|
T | C | 200 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.715-15999T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445405 | ||||||
| chr16:445538
|
C | T | 190 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0115others(187): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.715-15866C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445538 | ||||||
| chr16:445563
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.715-15841C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445563 | ||||||
| chr16:445662
|
T | C | 96 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0118others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.715-15742T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445662 | ||||||
| chr16:445950
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-15454C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445950 | ||||||
| chr16:445993
|
A | G | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.715-15411A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 445993 | ||||||
| chr16:446022
|
T | C | 3 | a0001c0001t0015g0136a0001c0001t0041g0126a0001c0001t0056g0124 | 3 | HG02572.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.715-15382T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446022 | ||||||
| chr16:446104
|
T | G | 1 | a0001c0001t0003g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.715-15300T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446104 | ||||||
| chr16:446341
|
C | A | 1 | a0001c0001t0006g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.715-15063C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446341 | ||||||
| chr16:446349
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-15055G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446349 | ||||||
| chr16:446703
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.715-14700_715-1468 others(16): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446703 | ||||||
| chr16:446782
|
G | A | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-14622G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446782 | ||||||
| chr16:446823
|
C | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-14581C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446823 | ||||||
| chr16:446826
|
G | T | 1 | a0001c0001t0003g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.715-14578G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446826 | ||||||
| chr16:446902
|
T | C | 4 | a0001c0001t0015g0039a0001c0001t0023g0036a0001c0002t0009g0040others(1): Show | 4 | HG01243.hp1 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-14502T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446902 | ||||||
| chr16:446950
|
C | T | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.715-14454C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446950 | ||||||
| chr16:446985
|
C | T | 2 | a0001c0001t0013g0029a0001c0001t0013g0033 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.715-14419C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 446985 | ||||||
| chr16:447040
|
C | G | 21 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(18): Show | 21 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-14364C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447040 | ||||||
| chr16:447164
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-14240G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447164 | ||||||
| chr16:447229
|
C | G | 1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.715-14175C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447229 | ||||||
| chr16:447296
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.715-14108C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447296 | ||||||
| chr16:447343
|
G | A | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-14061G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447343 | ||||||
| chr16:447517
|
C | T | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.715-13887C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447517 | ||||||
| chr16:447533
|
C | T | 1 | a0006c0010t0005g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.715-13871C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447533 | ||||||
| chr16:447702
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0240 | 2 | HG00597.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.715-13702C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447702 | ||||||
| chr16:447721
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-13683G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447721 | ||||||
| chr16:447813
|
A | G | 1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.715-13591A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447813 | ||||||
| chr16:447877
|
T | C | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.715-13527T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447877 | ||||||
| chr16:447894
|
T | A | 1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.715-13510T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447894 | ||||||
| chr16:447930
|
A | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0240a0001c0001t0001g0245others(2): Show | 5 | HG00423.hp1 HG00597.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-13474A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447930 | ||||||
| chr16:447948
|
C | T | 5 | a0001c0001t0015g0123a0001c0001t0015g0127a0001c0001t0015g0184others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-13456C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 447948 | ||||||
| chr16:447990
|
AAG | A | 76 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.715-13412_715-1341 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 447990 | |||||
| chr16:448146
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-13258A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448146 | ||||||
| chr16:448168
|
T | G | 1 | a0001c0001t0010g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.715-13236T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448168 | ||||||
| chr16:448355
|
G | A | 5 | a0001c0001t0001g0182a0001c0001t0006g0187a0001c0001t0010g0188others(2): Show | 5 | HG02109.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-13049G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448355 | ||||||
| chr16:448536
|
A | T | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.715-12868A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448536 | ||||||
| chr16:448552
|
C | T | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.715-12852C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448552 | ||||||
| chr16:448564
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-12840T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448564 | ||||||
| chr16:448593
|
G | A | 1 | a0001c0001t0010g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.715-12811G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448593 | ||||||
| chr16:448617
|
T | C | 1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.715-12787T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448617 | ||||||
| chr16:448664
|
A | G | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-12740A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 448664 | ||||||
| chr16:448738
|
G | GA | 10 | a0001c0001t0001g0182a0001c0001t0001g0197a0001c0001t0001g0200others(7): Show | 10 | HG01256.hp2 HG01361.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-12646dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 448738 | |||||
| chr16:448738
|
GA | G | 103 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-12646delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 448738 | |||||
| chr16:448738
|
GAA | G | 49 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0015others(46): Show | 49 | HG00544.hp2 HG00609.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.715-12647_715-1264 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 448738 | |||||
| chr16:448906
|
ACT | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-12495_715-1249 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 448906 | |||||
| chr16:448932
|
CATAAATA others(5): Show |
C | 2 | a0001c0001t0010g0004a0001c0001t0016g0003 | 2 | HG00423.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.715-12454_715-1244 others(16): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 448932 | |||||
| chr16:449213
|
C | T | 3 | a0001c0002t0005g0070a0001c0002t0005g0075a0001c0002t0005g0079 | 3 | HG00323.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.715-12191C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449213 | ||||||
| chr16:449279
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.715-12125G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449279 | ||||||
| chr16:449292
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-12112G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449292 | ||||||
| chr16:449348
|
C | G | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.715-12056C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449348 | ||||||
| chr16:449470
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.715-11934C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449470 | ||||||
| chr16:449491
|
T | G | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0012t0059g0107 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.715-11913T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449491 | ||||||
| chr16:449500
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-11904G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449500 | ||||||
| chr16:449531
|
A | G | 82 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.715-11873A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449531 | ||||||
| chr16:449646
|
C | CA | 87 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0286others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-11741dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 449646 | |||||
| chr16:449646
|
CA | C | 6 | a0001c0001t0001g0206a0001c0001t0001g0232a0001c0001t0035g0045others(3): Show | 6 | HG01928.hp1 HG02257.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-11741delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 449646 | |||||
| chr16:449722
|
T | C | 1 | a0001c0001t0002g0015 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.715-11682T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449722 | ||||||
| chr16:449809
|
T | C | 186 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(183): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.715-11595T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449809 | ||||||
| chr16:449876
|
G | A | 1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-11528G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449876 | ||||||
| chr16:449882
|
CA | C | 82 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.715-11521delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449882 | ||||||
| chr16:449883
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.715-11521A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449883 | ||||||
| chr16:449931
|
A | T | 1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.715-11473A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449931 | ||||||
| chr16:449999
|
G | A | 11 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(8): Show | 11 | HG01261.hp2 HG02280.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-11405G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 449999 | ||||||
| chr16:450031
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0025g0021a0001c0001t0025g0109others(4): Show | 7 | HG02717.hp1 HG02970.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-11373C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450031 | ||||||
| chr16:450398
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-11006T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450398 | ||||||
| chr16:450443
|
G | A | 5 | a0001c0001t0008g0294a0001c0001t0025g0021a0001c0001t0025g0109others(2): Show | 5 | HG02970.hp2 HG03579.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-10961G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450443 | ||||||
| chr16:450505
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-10899T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450505 | ||||||
| chr16:450532
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.715-10872G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450532 | ||||||
| chr16:450648
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-10756T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450648 | ||||||
| chr16:450669
|
G | A | 1 | a0001c0001t0020g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.715-10735G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450669 | ||||||
| chr16:450705
|
C | G | 1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.715-10699C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450705 | ||||||
| chr16:450739
|
T | G | 1 | a0001c0002t0030g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.715-10665T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450739 | ||||||
| chr16:450806
|
C | T | 1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.715-10598C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450806 | ||||||
| chr16:450838
|
C | G | 5 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0001t0060g0108others(2): Show | 5 | HG02976.hp2 HG03579.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-10566C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450838 | ||||||
| chr16:450839
|
G | C | 1 | a0001c0001t0014g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.715-10565G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450839 | ||||||
| chr16:450839
|
G | GC | 108 | a0001c0001t0001g0006a0001c0001t0001g0144a0001c0001t0001g0145others(105): Show | 109 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.715-10559dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 450839 | |||||
| chr16:450847
|
C | T | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.715-10557C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 450847 | ||||||
| chr16:451066
|
CTGTTTTC others(10): Show |
C | 1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.715-10337_715-1032 others(21): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451066 | ||||||
| chr16:451155
|
A | T | 42 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.715-10249A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451155 | ||||||
| chr16:451314
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-10090C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451314 | ||||||
| chr16:451362
|
C | T | 81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.715-10042C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451362 | ||||||
| chr16:451369
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-10035C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451369 | ||||||
| chr16:451447
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-9957C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451447 | ||||||
| chr16:451448
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.715-9956G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451448 | ||||||
| chr16:451600
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-9804T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451600 | ||||||
| chr16:451638
|
C | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-9766C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451638 | ||||||
| chr16:451877
|
C | T | 1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.715-9527C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 451877 | ||||||
| chr16:452010
|
G | A | 1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.715-9394G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452010 | ||||||
| chr16:452074
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-9330C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452074 | ||||||
| chr16:452108
|
G | A | 1 | a0001c0001t0008g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.715-9296G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452108 | ||||||
| chr16:452318
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.715-9086G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452318 | ||||||
| chr16:452414
|
C | G | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.715-8990C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452414 | ||||||
| chr16:452426
|
T | TTTA | 3 | a0001c0001t0021g0001a0001c0006t0032g0270a0001c0008t0057g0113 | 4 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-8957_715-8955d others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 452426 | |||||
| chr16:452535
|
C | T | 1 | a0001c0002t0009g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.715-8869C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452535 | ||||||
| chr16:452545
|
CTGCCTCA others(313): Show |
C | 171 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(168): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.715-8529_715-8210d others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 452545 | |||||
| chr16:452864
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.715-8540C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452864 | ||||||
| chr16:452907
|
A | T | 7 | a0001c0001t0001g0214a0001c0001t0001g0223a0001c0001t0001g0229others(4): Show | 7 | HG00408.hp2 HG02132.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-8497A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452907 | ||||||
| chr16:452915
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.715-8489C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452915 | ||||||
| chr16:452920
|
A | C | 3 | a0001c0004t0008g0172a0002c0003t0002g0093a0002c0003t0002g0094 | 3 | NA18947.hp1 NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.715-8484A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 452920 | ||||||
| chr16:453016
|
A | G | 5 | a0001c0001t0015g0123a0001c0001t0015g0127a0001c0001t0015g0184others(2): Show | 5 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-8388A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453016 | ||||||
| chr16:453046
|
G | A | 48 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-8358G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453046 | ||||||
| chr16:453050
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-8354G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453050 | ||||||
| chr16:453098
|
C | T | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.715-8306C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453098 | ||||||
| chr16:453099
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.715-8305G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453099 | ||||||
| chr16:453125
|
G | T | 2 | a0001c0002t0009g0081a0006c0010t0005g0080 | 2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.715-8279G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453125 | ||||||
| chr16:453310
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0010g0004a0001c0001t0016g0003others(1): Show | 4 | HG00423.hp2 NA18949.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-8094G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453310 | ||||||
| chr16:453321
|
G | A | 27 | a0001c0001t0001g0140a0001c0001t0003g0125a0001c0001t0003g0133others(24): Show | 27 | HG00544.hp2 HG00609.hp1 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.715-8083G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453321 | ||||||
| chr16:453353
|
T | C | 144 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.715-8051T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453353 | ||||||
| chr16:453369
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-8035C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453369 | ||||||
| chr16:453481
|
T | C | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-7923T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453481 | ||||||
| chr16:453586
|
G | GT | 70 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0117others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.715-7797dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 453586 | |||||
| chr16:453586
|
G | GTT | 9 | a0001c0001t0004g0090a0001c0001t0004g0178a0001c0001t0008g0068others(6): Show | 9 | HG01109.hp2 HG02083.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-7798_715-7797d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 453586 | |||||
| chr16:453586
|
GT | G | 18 | a0001c0001t0001g0119a0001c0001t0001g0245a0001c0001t0007g0016others(15): Show | 18 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.715-7797delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 453586 | |||||
| chr16:453597
|
T | G | 6 | a0001c0001t0015g0122a0001c0001t0015g0136a0001c0001t0033g0128others(3): Show | 6 | HG02572.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-7807T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453597 | ||||||
| chr16:453597
|
T | TG | 37 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.715-7807_715-7806i others(3): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453597 | ||||||
| chr16:453597
|
T | TGTTTTGT others(4): Show |
2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-7807_715-7806i others(13): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453597 | ||||||
| chr16:453602
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-7802T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453602 | ||||||
| chr16:453693
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.715-7711C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453693 | ||||||
| chr16:453753
|
G | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0251 | 2 | HG01361.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.715-7651G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 453753 | ||||||
| chr16:453947
|
AT | A | 171 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(168): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.715-7454delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 453947 | |||||
| chr16:454022
|
C | T | 1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.715-7382C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454022 | ||||||
| chr16:454124
|
G | T | 1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.715-7280G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454124 | ||||||
| chr16:454133
|
T | C | 1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.715-7271T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454133 | ||||||
| chr16:454143
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-7261T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454143 | ||||||
| chr16:454172
|
C | A | 1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.715-7232C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454172 | ||||||
| chr16:454505
|
C | T | 3 | a0001c0002t0002g0158a0001c0002t0002g0171a0001c0002t0016g0156 | 3 | HG01109.hp1 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.715-6899C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454505 | ||||||
| chr16:454519
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-6885G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454519 | ||||||
| chr16:454768
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.715-6636C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454768 | ||||||
| chr16:454921
|
G | A | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-6483G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 454921 | ||||||
| chr16:455006
|
C | T | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.715-6398C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455006 | ||||||
| chr16:455049
|
C | CA | 24 | a0001c0001t0001g0203a0001c0001t0001g0234a0001c0001t0001g0259others(21): Show | 24 | HG00408.hp1 HG00609.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.715-6344dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 455049 | |||||
| chr16:455061
|
C | A | 162 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.715-6343C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455061 | ||||||
| chr16:455062
|
A | C | 11 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-6342A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455062 | ||||||
| chr16:455069
|
C | A | 2 | a0001c0001t0015g0184a0001c0001t0024g0185 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.715-6335C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455069 | ||||||
| chr16:455077
|
T | G | 4 | a0001c0001t0001g0159a0001c0001t0050g0168a0001c0006t0058g0111others(1): Show | 4 | HG02165.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-6327T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455077 | ||||||
| chr16:455205
|
C | T | 2 | a0001c0001t0006g0187a0001c0001t0010g0188 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.715-6199C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455205 | ||||||
| chr16:455218
|
G | A | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-6186G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455218 | ||||||
| chr16:455252
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-6152G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455252 | ||||||
| chr16:455252
|
G | T | 1 | a0001c0001t0012g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.715-6152G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455252 | ||||||
| chr16:455334
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-6070C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455334 | ||||||
| chr16:455398
|
C | T | 2 | a0001c0002t0009g0081a0006c0010t0005g0080 | 2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.715-6006C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455398 | ||||||
| chr16:455432
|
C | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.715-5972C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455432 | ||||||
| chr16:455472
|
CA | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0228a0001c0001t0002g0176others(4): Show | 7 | HG01071.hp1 HG02896.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-5916delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 455472 | |||||
| chr16:455501
|
G | A | 1 | a0001c0001t0010g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.715-5903G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455501 | ||||||
| chr16:455605
|
T | C | 48 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-5799T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455605 | ||||||
| chr16:455609
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.715-5795T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455609 | ||||||
| chr16:455612
|
T | G | 57 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(54): Show | 57 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.715-5792T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455612 | ||||||
| chr16:455642
|
G | A | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.715-5762G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455642 | ||||||
| chr16:455656
|
C | T | 2 | a0001c0001t0014g0142a0001c0001t0014g0143 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.715-5748C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455656 | ||||||
| chr16:455669
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.715-5735C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455669 | ||||||
| chr16:455672
|
T | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-5732T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455672 | ||||||
| chr16:455791
|
A | T | 1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.715-5613A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455791 | ||||||
| chr16:455819
|
G | A | 1 | a0001c0001t0041g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.715-5585G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455819 | ||||||
| chr16:455882
|
T | C | 1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.715-5522T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455882 | ||||||
| chr16:455954
|
C | T | 4 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025others(1): Show | 4 | HG03579.hp1 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-5450C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455954 | ||||||
| chr16:455998
|
A | G | 2 | a0001c0001t0020g0247a0007c0015t0020g0199 | 2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.715-5406A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 455998 | ||||||
| chr16:456060
|
G | A | 1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.715-5344G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456060 | ||||||
| chr16:456407
|
C | T | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-4997C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456407 | ||||||
| chr16:456435
|
G | T | 1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.715-4969G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456435 | ||||||
| chr16:456439
|
C | CA | 9 | a0001c0001t0005g0013a0001c0001t0011g0110a0001c0001t0012g0104others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-4952dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 456439 | |||||
| chr16:456510
|
A | G | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.715-4894A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456510 | ||||||
| chr16:456512
|
T | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-4892T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456512 | ||||||
| chr16:456535
|
C | T | 1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-4869C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456535 | ||||||
| chr16:456612
|
A | G | 182 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.715-4792A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456612 | ||||||
| chr16:456699
|
G | A | 1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.715-4705G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456699 | ||||||
| chr16:456783
|
A | C | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.715-4621A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456783 | ||||||
| chr16:456786
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.715-4618C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 456786 | ||||||
| chr16:457131
|
G | A | 1 | a0001c0001t0017g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.715-4273G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457131 | ||||||
| chr16:457139
|
G | A | 1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.715-4265G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457139 | ||||||
| chr16:457168
|
T | C | 10 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103others(7): Show | 10 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.715-4236T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457168 | ||||||
| chr16:457283
|
T | A | 1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.715-4121T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457283 | ||||||
| chr16:457290
|
T | C | 12 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-4114T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457290 | ||||||
| chr16:457511
|
C | CT | 73 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0162others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-3878dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 457511 | |||||
| chr16:457621
|
G | C | 11 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-3783G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457621 | ||||||
| chr16:457724
|
G | A | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-3680G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457724 | ||||||
| chr16:457795
|
G | A | 1 | a0001c0001t0006g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.715-3609G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457795 | ||||||
| chr16:457816
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-3588C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457816 | ||||||
| chr16:457904
|
T | C | 12 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-3500T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457904 | ||||||
| chr16:457983
|
C | G | 2 | a0002c0003t0002g0093a0002c0003t0002g0094 | 2 | NA18947.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.715-3421C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 457983 | ||||||
| chr16:458103
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.715-3301C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458103 | ||||||
| chr16:458119
|
G | A | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-3285G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458119 | ||||||
| chr16:458159
|
A | T | 1 | a0001c0001t0013g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.715-3245A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458159 | ||||||
| chr16:458195
|
G | C | 1 | a0001c0004t0003g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.715-3209G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458195 | ||||||
| chr16:458217
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.715-3187G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458217 | ||||||
| chr16:458264
|
C | T | 4 | a0001c0001t0008g0294a0001c0001t0042g0085a0001c0006t0058g0111others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-3140C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458264 | ||||||
| chr16:458285
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-3119T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458285 | ||||||
| chr16:458304
|
G | A | 30 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(27): Show | 30 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.715-3100G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458304 | ||||||
| chr16:458395
|
A | AGGGGGCC others(70): Show |
1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.715-2966_715-2965i others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
A | AGGGGGCC others(71): Show |
10 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(7): Show | 10 | HG01261.hp2 HG02717.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2864_715-2787d others(80): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
A | AGGGGGCC others(539): Show |
2 | a0001c0001t0012g0030a0001c0001t0012g0031 | 2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
A | AGGGGGCC others(539): Show |
2 | a0001c0001t0010g0032a0001c0001t0010g0046 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.715-2784_715-2783i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
A | AGGGGGCC others(773): Show |
1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.715-2784_715-2783i others(782): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
A | AGGGGGCC others(539): Show |
2 | a0001c0001t0008g0068a0001c0001t0011g0179 | 2 | NA18967.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.715-2904_715-2903i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
AGGGGGCC others(32): Show |
A | 4 | a0001c0001t0010g0222a0001c0002t0019g0106a0001c0002t0053g0271others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2825_715-2787d others(41): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458395
|
AGGGGGCC others(71): Show |
A | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.715-2864_715-2787d others(80): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458395 | |||||
| chr16:458405
|
C | CCTCGGGT others(305): Show |
1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.715-2911_715-2910i others(314): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458405 | |||||
| chr16:458423
|
C | CCACAGGG others(539): Show |
1 | a0001c0001t0003g0060 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.715-2872_715-2871i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458423 | |||||
| chr16:458423
|
C | CCACAGGG others(1124): Show |
1 | a0001c0001t0017g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.715-2872_715-2871i others(1133): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458423 | |||||
| chr16:458423
|
C | CCACAGGG others(695): Show |
1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715-2911_715-2910i others(704): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458423 | |||||
| chr16:458423
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-2981C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458423 | ||||||
| chr16:458447
|
C | T | 1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-2957C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458447 | ||||||
| chr16:458462
|
C | CCACAGGG others(227): Show |
6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-2784_715-2783i others(236): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458462 | |||||
| chr16:458462
|
C | CCACAGGG others(812): Show |
1 | a0001c0001t0004g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.715-2872_715-2871i others(821): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458462 | |||||
| chr16:458462
|
C | CCACAGGG others(695): Show |
1 | a0001c0001t0051g0064 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.715-2904_715-2903i others(704): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458462 | |||||
| chr16:458462
|
C | CCACAGGG others(3464): Show |
1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.715-2911_715-2910i others(3473): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458462 | |||||
| chr16:458462
|
C | CCACCAGG others(228): Show |
1 | a0001c0001t0008g0063 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.715-2939_715-2938i others(237): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458462 | |||||
| chr16:458501
|
C | CCACAGGG others(226): Show |
1 | a0001c0001t0023g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-2888_715-2887i others(235): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(187): Show |
1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.715-2849_715-2848i others(196): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(1943): Show |
1 | a0001c0001t0060g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1952): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(1163): Show |
1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(500): Show |
1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.715-2871_715-2870i others(509): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(812): Show |
1 | a0001c0001t0055g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.715-2872_715-2871i others(821): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | CCACAGGG others(695): Show |
2 | a0001c0001t0003g0180a0001c0001t0003g0213 | 2 | NA18939.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.715-2872_715-2871i others(704): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458501 | |||||
| chr16:458501
|
C | T | 7 | a0001c0001t0008g0065a0001c0001t0008g0068a0001c0001t0011g0179others(4): Show | 7 | HG00323.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-2903C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458501 | ||||||
| chr16:458526
|
G | A | 1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-2878G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458526 | ||||||
| chr16:458528
|
G | A | 1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-2876G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458528 | ||||||
| chr16:458528
|
G | GTTCAGTG others(851): Show |
1 | a0001c0001t0017g0087 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.715-2872_715-2871i others(860): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458528 | |||||
| chr16:458528
|
G | GTTCAGTG others(1748): Show |
1 | a0001c0001t0017g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.715-2872_715-2871i others(1757): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458528 | |||||
| chr16:458528
|
G | GTTCAGTG others(1670): Show |
1 | a0001c0001t0017g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.715-2872_715-2871i others(1679): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458528 | |||||
| chr16:458533
|
C | G | 3 | a0001c0001t0042g0085a0001c0006t0058g0111a0001c0008t0057g0113 | 3 | HG01109.hp2 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-2871C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458533 | ||||||
| chr16:458534
|
C | CGATGCCC others(344): Show |
1 | a0001c0001t0004g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(353): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458534 | |||||
| chr16:458534
|
C | T | 8 | a0001c0001t0017g0049a0001c0001t0017g0061a0001c0001t0017g0087others(5): Show | 8 | HG00323.hp2 HG01109.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-2870C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458534 | ||||||
| chr16:458540
|
C | CCACAGGG others(2450): Show |
1 | a0001c0001t0010g0004 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.715-2849_715-2848i others(2459): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(3387): Show |
1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.715-2849_715-2848i others(3396): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(2294): Show |
1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.715-2849_715-2848i others(2303): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(2684): Show |
1 | a0001c0001t0002g0002 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.715-2849_715-2848i others(2693): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(2762): Show |
1 | a0001c0001t0016g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.715-2849_715-2848i others(2771): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(226): Show |
1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.715-2849_715-2848i others(235): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(382): Show |
1 | a0001c0001t0015g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.715-2849_715-2848i others(391): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(265): Show |
5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0002t0009g0040others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-2849_715-2848i others(274): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(343): Show |
1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.715-2849_715-2848i others(352): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(890): Show |
1 | a0001c0001t0008g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.715-2840_715-2839i others(899): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(929): Show |
1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-2832_715-2831i others(938): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(1436): Show |
1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1445): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | CCACAGGG others(4205): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(4214): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458540 | |||||
| chr16:458540
|
C | T | 9 | a0001c0001t0003g0180a0001c0001t0003g0213a0001c0001t0017g0049others(6): Show | 9 | HG00323.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-2864C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458540 | ||||||
| chr16:458556
|
G | A | 31 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0010others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.715-2848G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458556 | ||||||
| chr16:458565
|
G | A | 8 | a0001c0001t0003g0060a0001c0001t0004g0055a0001c0001t0008g0068others(5): Show | 8 | HG01928.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-2839G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458565 | ||||||
| chr16:458567
|
G | A | 8 | a0001c0001t0003g0060a0001c0001t0004g0055a0001c0001t0008g0068others(5): Show | 8 | HG01928.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-2837G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458567 | ||||||
| chr16:458567
|
G | GTTCAGTG others(890): Show |
1 | a0001c0001t0004g0056 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(899): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(2099): Show |
1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(2108): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(968): Show |
1 | a0001c0002t0005g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(977): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1007): Show |
1 | a0001c0002t0005g0079 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1016): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1007): Show |
1 | a0001c0002t0005g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1016): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(2490): Show |
1 | a0001c0001t0008g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(2499): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1163): Show |
1 | a0001c0001t0001g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1748): Show |
1 | a0001c0001t0008g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1757): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(2099): Show |
1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(2108): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1241): Show |
1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1250): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1007): Show |
1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1016): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1475): Show |
1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1484): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(734): Show |
2 | a0001c0001t0004g0088a0001c0001t0004g0090 | 2 | HG02083.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.715-2833_715-2832i others(743): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(461): Show |
1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(470): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(499): Show |
1 | a0001c0001t0004g0054 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(508): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(929): Show |
1 | a0001c0001t0028g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(938): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(500): Show |
1 | a0001c0001t0004g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(509): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(539): Show |
1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(578): Show |
2 | a0001c0001t0004g0059a0001c0001t0007g0053 | 2 | HG00544.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.715-2833_715-2832i others(587): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1007): Show |
1 | a0001c0001t0004g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1016): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(4478): Show |
1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.715-2833_715-2832i others(4487): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458567
|
G | GTTCAGTG others(1943): Show |
1 | a0004c0007t0022g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.715-2833_715-2832i others(1952): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458567 | |||||
| chr16:458572
|
C | G | 2 | a0001c0001t0025g0021a0001c0002t0043g0025 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.715-2832C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458572 | ||||||
| chr16:458573
|
C | CGATGCCC others(383): Show |
1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(392): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458573 | |||||
| chr16:458573
|
C | CGATGCTC others(71): Show |
1 | a0001c0001t0008g0063 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.715-2826_715-2825i others(80): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458573 | |||||
| chr16:458573
|
C | T | 36 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(33): Show | 36 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.715-2831C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458573 | ||||||
| chr16:458578
|
C | T | 2 | a0001c0001t0025g0021a0001c0002t0043g0025 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.715-2826C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458578 | ||||||
| chr16:458579
|
C | CCACAGGG others(1865): Show |
1 | a0006c0010t0005g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.715-2801_715-2800i others(1874): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458579 | |||||
| chr16:458579
|
C | CCACAGGG others(929): Show |
1 | a0001c0001t0003g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(938): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458579 | |||||
| chr16:458579
|
C | CCACAGGG others(2918): Show |
1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2927): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458579 | |||||
| chr16:458579
|
C | CCACAGGG others(2177): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2186): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458579 | |||||
| chr16:458579
|
C | T | 61 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0002others(58): Show | 61 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.715-2825C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458579 | ||||||
| chr16:458604
|
G | A | 3 | a0001c0001t0025g0021a0001c0002t0043g0025a0005c0017t0037g0100 | 3 | HG02717.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.715-2800G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458604 | ||||||
| chr16:458604
|
G | GGGTTCAC others(929): Show |
1 | a0001c0001t0003g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(938): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2528): Show |
2 | a0001c0001t0002g0017a0001c0011t0002g0019 | 2 | NA18950.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(2537): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1943): Show |
1 | a0001c0001t0005g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1952): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1553): Show |
2 | a0001c0001t0004g0018a0001c0001t0007g0016 | 2 | NA18990.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1562): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2372): Show |
1 | a0001c0001t0033g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2381): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2255): Show |
1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2264): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2840): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2849): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2333): Show |
1 | a0001c0001t0056g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2342): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1904): Show |
1 | a0001c0001t0041g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1913): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2255): Show |
1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2264): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(968): Show |
1 | a0001c0001t0003g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(977): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(929): Show |
1 | a0001c0001t0003g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(938): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1787): Show |
1 | a0001c0001t0002g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1796): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2157): Show |
1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2166): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(383): Show |
1 | a0001c0001t0002g0015 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(392): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(422): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(431): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(227): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(236): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1163): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1592): Show |
1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1601): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1904): Show |
1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1913): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1475): Show |
1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1484): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1709): Show |
1 | a0001c0002t0002g0152 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1718): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1358): Show |
1 | a0001c0001t0014g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1367): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1670): Show |
1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1679): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1710): Show |
1 | a0001c0002t0002g0146 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1719): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(500): Show |
1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(509): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2723): Show |
1 | a0001c0002t0002g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2732): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2762): Show |
1 | a0001c0002t0002g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2771): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2801): Show |
1 | a0001c0002t0016g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2810): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2762): Show |
1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2771): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(3386): Show |
1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(3395): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2489): Show |
1 | a0001c0002t0002g0153 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2498): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2489): Show |
1 | a0001c0002t0002g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2498): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2567): Show |
1 | a0001c0002t0030g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2576): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2528): Show |
1 | a0001c0002t0016g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2537): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2762): Show |
1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2771): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2528): Show |
1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2537): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2645): Show |
1 | a0001c0001t0002g0176 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2654): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2372): Show |
1 | a0001c0001t0002g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2381): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(3425): Show |
1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(3434): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2294): Show |
1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2303): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2021): Show |
1 | a0001c0002t0002g0167 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2030): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2060): Show |
1 | a0001c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2069): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1319): Show |
1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1328): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2060): Show |
1 | a0001c0002t0002g0255 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2069): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(3347): Show |
1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(3356): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2021): Show |
1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2030): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1631): Show |
1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1640): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(2574): Show |
1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(2583): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(734): Show |
1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(743): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(539): Show |
1 | a0001c0001t0015g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(578): Show |
1 | a0001c0001t0015g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(587): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1163): Show |
5 | a0001c0001t0003g0216a0001c0001t0011g0132a0001c0001t0045g0138others(2): Show | 5 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1202): Show |
1 | a0001c0001t0001g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1211): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1202): Show |
5 | a0001c0001t0003g0125a0001c0001t0003g0235a0001c0001t0007g0047others(2): Show | 5 | HG00544.hp2 HG02074.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1211): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1046): Show |
1 | a0001c0001t0047g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1055): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1241): Show |
1 | a0001c0001t0003g0133 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1250): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1241): Show |
1 | a0001c0001t0003g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1250): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1163): Show |
2 | a0001c0001t0003g0135a0001c0001t0007g0134 | 2 | HG02165.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1280): Show |
1 | a0001c0001t0003g0211 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1289): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1163): Show |
3 | a0001c0001t0003g0210a0001c0001t0003g0261a0001c0001t0034g0208 | 3 | NA18977.hp1 NA18983.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1163): Show |
2 | a0002c0003t0007g0095a0002c0003t0007g0096 | 2 | NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1203): Show |
1 | a0001c0001t0007g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1212): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(773): Show |
1 | a0001c0001t0023g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(782): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1865): Show |
1 | a0001c0001t0011g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1874): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(1982): Show |
1 | a0001c0001t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.715-2787_715-2786i others(1991): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(110): Show |
1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(119): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(656): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-2787_715-2786i others(665): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAC others(539): Show |
2 | a0001c0001t0015g0184a0001c0001t0024g0185 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.715-2787_715-2786i others(548): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAG others(1007): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.715-2794_715-2793i others(1016): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458604
|
G | GGGTTCAG others(1397): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.715-2794_715-2793i others(1406): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 458604 | |||||
| chr16:458642
|
C | T | 3 | a0001c0001t0011g0110a0001c0001t0012g0104a0001c0001t0023g0103 | 3 | HG01891.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.715-2762C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458642 | ||||||
| chr16:458674
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-2730A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458674 | ||||||
| chr16:458676
|
A | G | 88 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.715-2728A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458676 | ||||||
| chr16:458715
|
T | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-2689T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458715 | ||||||
| chr16:458771
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-2633C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458771 | ||||||
| chr16:458789
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.715-2615C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458789 | ||||||
| chr16:458950
|
G | T | 1 | a0001c0001t0021g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.715-2454G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 458950 | ||||||
| chr16:459086
|
A | T | 10 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2318A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459086 | ||||||
| chr16:459087
|
G | T | 10 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2317G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459087 | ||||||
| chr16:459124
|
C | CT | 6 | a0001c0001t0001g0259a0001c0001t0003g0260a0001c0001t0005g0014others(3): Show | 6 | HG02080.hp1 HG02738.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-2261dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 459124 | |||||
| chr16:459124
|
CT | C | 23 | a0001c0001t0006g0187a0001c0001t0011g0110a0001c0001t0012g0104others(20): Show | 23 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.715-2261delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 459124 | |||||
| chr16:459353
|
G | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-2051G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459353 | ||||||
| chr16:459377
|
C | T | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.715-2027C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459377 | ||||||
| chr16:459381
|
C | T | 1 | a0001c0002t0002g0167 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.715-2023C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459381 | ||||||
| chr16:459431
|
C | CT | 12 | a0001c0001t0008g0294a0001c0001t0013g0027a0001c0001t0025g0021others(9): Show | 12 | HG01106.hp1 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-1952dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 459431 | |||||
| chr16:459431
|
CT | C | 60 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0224others(57): Show | 60 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.715-1952delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 459431 | |||||
| chr16:459463
|
T | G | 60 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(57): Show | 60 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.715-1941T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459463 | ||||||
| chr16:459501
|
A | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-1903A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459501 | ||||||
| chr16:459557
|
C | G | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.715-1847C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459557 | ||||||
| chr16:459671
|
C | T | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.715-1733C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459671 | ||||||
| chr16:459759
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.715-1645G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459759 | ||||||
| chr16:459825
|
A | G | 1 | a0001c0001t0020g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.715-1579A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459825 | ||||||
| chr16:459875
|
C | CT | 16 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0003g0135others(13): Show | 16 | HG01175.hp2 HG01261.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.715-1509dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 459875 | |||||
| chr16:459934
|
A | G | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.715-1470A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459934 | ||||||
| chr16:459982
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.715-1422A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 459982 | ||||||
| chr16:460036
|
C | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.715-1368C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460036 | ||||||
| chr16:460096
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.715-1308G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460096 | ||||||
| chr16:460149
|
A | T | 1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.715-1255A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460149 | ||||||
| chr16:460417
|
C | T | 37 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.715-987C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460417 | ||||||
| chr16:460443
|
T | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-961T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460443 | ||||||
| chr16:460460
|
C | G | 2 | a0001c0001t0002g0017a0001c0011t0002g0019 | 2 | NA18950.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.715-944C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460460 | ||||||
| chr16:460550
|
C | T | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-854C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460550 | ||||||
| chr16:460634
|
G | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-770G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460634 | ||||||
| chr16:460679
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.715-725G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460679 | ||||||
| chr16:460703
|
A | G | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.715-701A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460703 | ||||||
| chr16:460873
|
G | A | 6 | a0001c0001t0015g0122a0001c0001t0015g0136a0001c0001t0033g0128others(3): Show | 6 | HG02572.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-531G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460873 | ||||||
| chr16:460876
|
C | CTGTGGCT others(96): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-516_715-515ins others(103): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 460876 | |||||
| chr16:460889
|
C | T | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-515C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460889 | ||||||
| chr16:460929
|
G | A | 9 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(6): Show | 9 | HG01261.hp2 HG02717.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-475G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460929 | ||||||
| chr16:460961
|
G | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.715-443G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 460961 | ||||||
| chr16:460961
|
G | GCCCCTGT others(96): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-424_715-423ins others(103): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 460961 | |||||
| chr16:461080
|
C | T | 65 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.715-324C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 461080 | ||||||
| chr16:461094
|
C | T | 15 | a0001c0001t0001g0268a0001c0001t0008g0265a0001c0001t0010g0032others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-310C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 461094 | ||||||
| chr16:461103
|
C | T | 35 | a0001c0001t0001g0140a0001c0001t0002g0015a0001c0001t0002g0017others(32): Show | 35 | HG00544.hp2 HG00609.hp1 HG01981.hp1 others(32): Show |
intron_variant | MODIFIER | c.715-301C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 461103 | ||||||
| chr16:461183
|
G | T | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-221G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 461183 | ||||||
| chr16:461337
|
G | C | 18 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0118others(15): Show | 18 | HG00438.hp2 HG00597.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.715-67G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 1/13 | chr16 | 461337 | ||||||
| chr16:461535
|
C | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.808+38C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 461535 | ||||||
| chr16:461763
|
A | C | 15 | a0001c0001t0001g0268a0001c0001t0008g0265a0001c0001t0010g0032others(12): Show | 15 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+266A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 461763 | ||||||
| chr16:461936
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+439T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 461936 | ||||||
| chr16:461967
|
C | T | 13 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(10): Show | 13 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.808+470C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 461967 | ||||||
| chr16:462031
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.808+534C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462031 | ||||||
| chr16:462095
|
A | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+598A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462095 | ||||||
| chr16:462096
|
G | A | 1 | a0001c0002t0053g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.808+599G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462096 | ||||||
| chr16:462375
|
C | T | 2 | a0001c0001t0008g0065a0001c0001t0051g0064 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.808+878C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462375 | ||||||
| chr16:462443
|
G | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.808+946G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462443 | ||||||
| chr16:462575
|
C | T | 1 | a0001c0001t0056g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808+1078C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462575 | ||||||
| chr16:462584
|
T | TTTCTCCT others(12): Show |
1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.808+1090_808+1091i others(21): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462584 | |||||
| chr16:462589
|
T | C | 1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.808+1092T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462589 | ||||||
| chr16:462589
|
T | TCAGCACG others(10): Show |
166 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.808+1116_808+1132d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462589 | |||||
| chr16:462613
|
GATCCCTT others(10): Show |
G | 9 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(6): Show | 9 | HG01261.hp2 HG02717.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+1143_808+1159d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462613 | |||||
| chr16:462630
|
C | G | 3 | a0001c0001t0003g0125a0001c0006t0058g0111a0001c0008t0057g0113 | 3 | HG02257.hp2 HG03041.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.808+1133C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462630 | ||||||
| chr16:462646
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1149C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462646 | ||||||
| chr16:462647
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1150C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462647 | ||||||
| chr16:462657
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1160G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462657 | ||||||
| chr16:462659
|
AGCACCGT others(10): Show |
A | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.808+1179_808+1195d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462659 | |||||
| chr16:462665
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1168G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462665 | ||||||
| chr16:462674
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1177C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462674 | ||||||
| chr16:462675
|
C | T | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.808+1178C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462675 | ||||||
| chr16:462676
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1179G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462676 | ||||||
| chr16:462700
|
C | T | 86 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.808+1203C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462700 | ||||||
| chr16:462753
|
G | A | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+1256G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462753 | ||||||
| chr16:462758
|
A | ATCCCTTC others(10): Show |
1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.808+1278_808+1294d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462758 | |||||
| chr16:462792
|
A | G | 2 | a0001c0001t0010g0195a0001c0002t0038g0038 | 2 | HG01243.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.808+1295A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462792 | ||||||
| chr16:462825
|
GATCCCTT others(10): Show |
G | 1 | a0001c0002t0038g0038 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.808+1355_808+1371d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462825 | |||||
| chr16:462869
|
TCAGCACA others(10): Show |
T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1396_808+1412d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462869 | |||||
| chr16:462918
|
T | TCCCAGCA others(10): Show |
2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1434_808+1435i others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 462918 | |||||
| chr16:462995
|
C | G | 176 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(173): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.808+1498C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 462995 | ||||||
| chr16:463091
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1594T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463091 | ||||||
| chr16:463130
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.808+1633G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463130 | ||||||
| chr16:463177
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1680A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463177 | ||||||
| chr16:463210
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.808+1713C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463210 | ||||||
| chr16:463295
|
G | A | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+1798G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463295 | ||||||
| chr16:463324
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+1827T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463324 | ||||||
| chr16:463409
|
C | A | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.808+1912C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463409 | ||||||
| chr16:463430
|
G | GT | 46 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0118others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.808+1958dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 463430 | |||||
| chr16:463430
|
G | T | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+1933G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463430 | ||||||
| chr16:463430
|
GT | G | 67 | a0001c0001t0001g0072a0001c0001t0001g0140a0001c0001t0002g0002others(64): Show | 68 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.808+1958delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 463430 | |||||
| chr16:463430
|
GTT | G | 61 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0017others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.808+1957_808+1958d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 463430 | |||||
| chr16:463430
|
GTTTTTTT others(2): Show |
G | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+1950_808+1958d others(11): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 463430 | |||||
| chr16:463596
|
G | A | 3 | a0003c0005t0014g0022a0003c0005t0014g0023a0003c0005t0014g0024 | 3 | HG03453.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.808+2099G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463596 | ||||||
| chr16:463746
|
A | G | 2 | a0001c0002t0019g0037a0001c0002t0019g0285 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.808+2249A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463746 | ||||||
| chr16:463770
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.808+2273C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 463770 | ||||||
| chr16:464010
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+2513T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464010 | ||||||
| chr16:464200
|
A | G | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.808+2703A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464200 | ||||||
| chr16:464344
|
A | G | 2 | a0001c0001t0003g0133a0001c0001t0003g0135 | 2 | NA18944.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.808+2847A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464344 | ||||||
| chr16:464346
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0242 | 3 | HG01175.hp2 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.808+2849C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464346 | ||||||
| chr16:464407
|
A | C | 168 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.808+2910A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464407 | ||||||
| chr16:464522
|
G | T | 1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.808+3025G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464522 | ||||||
| chr16:464631
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.808+3134C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464631 | ||||||
| chr16:464820
|
G | A | 9 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0023g0036others(6): Show | 9 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+3323G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464820 | ||||||
| chr16:464927
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.808+3430A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464927 | ||||||
| chr16:464934
|
T | C | 1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.808+3437T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464934 | ||||||
| chr16:464954
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.808+3457C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 464954 | ||||||
| chr16:465020
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+3523G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465020 | ||||||
| chr16:465054
|
T | C | 1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.808+3557T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465054 | ||||||
| chr16:465094
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+3597G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465094 | ||||||
| chr16:465154
|
G | A | 1 | a0009c0009t0003g0130 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.808+3657G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465154 | ||||||
| chr16:465221
|
A | T | 37 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(34): Show | 37 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.808+3724A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465221 | ||||||
| chr16:465267
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.808+3770C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465267 | ||||||
| chr16:465322
|
C | T | 39 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(36): Show | 39 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.808+3825C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465322 | ||||||
| chr16:465329
|
A | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+3832A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465329 | ||||||
| chr16:465346
|
A | G | 8 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0004g0018others(5): Show | 8 | HG03669.hp1 NA18950.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.808+3849A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465346 | ||||||
| chr16:465558
|
C | T | 1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.808+4061C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465558 | ||||||
| chr16:465572
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.808+4075A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465572 | ||||||
| chr16:465653
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.808+4156A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465653 | ||||||
| chr16:465699
|
T | C | 1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.808+4202T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465699 | ||||||
| chr16:465812
|
C | T | 2 | a0002c0003t0002g0093a0002c0003t0002g0094 | 2 | NA18947.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.808+4315C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465812 | ||||||
| chr16:465894
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+4397C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 465894 | ||||||
| chr16:466044
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.808+4547C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466044 | ||||||
| chr16:466127
|
T | C | 1 | a0001c0001t0003g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.808+4630T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466127 | ||||||
| chr16:466251
|
C | T | 20 | a0001c0001t0001g0140a0001c0001t0003g0125a0001c0001t0003g0133others(17): Show | 20 | HG00609.hp1 HG01981.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.808+4754C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466251 | ||||||
| chr16:466378
|
G | A | 1 | a0001c0001t0060g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.808+4881G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466378 | ||||||
| chr16:466389
|
G | A | 1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.808+4892G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466389 | ||||||
| chr16:466599
|
C | T | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-4696C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466599 | ||||||
| chr16:466713
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.809-4582C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466713 | ||||||
| chr16:466769
|
T | C | 3 | a0001c0006t0058g0111a0001c0008t0057g0113a0001c0014t0039g0112 | 3 | HG02257.hp2 HG03041.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.809-4526T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466769 | ||||||
| chr16:466909
|
T | C | 4 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025others(1): Show | 4 | HG03579.hp1 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-4386T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466909 | ||||||
| chr16:466922
|
T | G | 163 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.809-4373T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 466922 | ||||||
| chr16:467183
|
T | C | 46 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.809-4112T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467183 | ||||||
| chr16:467328
|
C | T | 6 | a0001c0001t0015g0122a0001c0001t0015g0136a0001c0001t0033g0128others(3): Show | 6 | HG02572.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3967C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467328 | ||||||
| chr16:467398
|
G | GGGAGGAG others(101): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.809-3816_809-3815i others(110): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467398 | |||||
| chr16:467408
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3887G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467408 | ||||||
| chr16:467460
|
C | CTCAGGGA others(783): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-3816_809-3815i others(792): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467460 | |||||
| chr16:467476
|
T | G | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809-3819T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467476 | ||||||
| chr16:467480
|
A | G | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809-3815A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467480 | ||||||
| chr16:467481
|
C | CGTCAGGG others(15): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3794_809-3793i others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467481 | |||||
| chr16:467498
|
A | AGGGGCGT others(15): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.809-3775_809-3754d others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467498 | |||||
| chr16:467498
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0040g0083a0001c0002t0019g0037 | 3 | HG02280.hp2 NA18971.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.809-3797A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467498 | ||||||
| chr16:467502
|
G | GCCTCAGG others(609): Show |
1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809-3792_809-3791i others(618): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467502 | |||||
| chr16:467504
|
G | C | 2 | a0001c0002t0019g0037a0001c0008t0057g0113 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.809-3791G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467504 | ||||||
| chr16:467520
|
G | A | 3 | a0001c0006t0058g0111a0001c0008t0057g0113a0001c0014t0039g0112 | 3 | HG02257.hp2 HG03041.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.809-3775G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467520 | ||||||
| chr16:467520
|
G | GGGGGCGT others(719): Show |
1 | a0001c0001t0004g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.809-3754_809-3753i others(728): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(697): Show |
1 | a0001c0001t0003g0060 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(706): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(587): Show |
6 | a0001c0001t0003g0180a0001c0001t0007g0053a0001c0001t0017g0061others(3): Show | 6 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3754_809-3753i others(596): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(697): Show |
10 | a0001c0001t0003g0213a0001c0001t0004g0051a0001c0001t0004g0054others(7): Show | 10 | HG00673.hp2 HG01975.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-3754_809-3753i others(706): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(983): Show |
1 | a0001c0001t0004g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(992): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(675): Show |
1 | a0001c0001t0017g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(684): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(698): Show |
1 | a0001c0001t0004g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(707): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(719): Show |
1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(728): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | GGGGGCGT others(125): Show |
1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3754_809-3753i others(134): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467520 | |||||
| chr16:467520
|
G | T | 2 | a0001c0001t0040g0083a0001c0002t0019g0037 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.809-3775G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467520 | ||||||
| chr16:467524
|
G | A | 1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-3771G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467524 | ||||||
| chr16:467524
|
G | GCGTCAGG others(631): Show |
2 | a0001c0002t0009g0081a0006c0010t0005g0080 | 2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.809-3754_809-3753i others(640): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467524 | |||||
| chr16:467524
|
G | GCGTCAGG others(169): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3754_809-3753i others(178): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467524 | |||||
| chr16:467525
|
C | CGTCAGGG others(15): Show |
2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3750_809-3749i others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467525 | |||||
| chr16:467526
|
G | C | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809-3769G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467526 | ||||||
| chr16:467526
|
G | GTCAGGGA others(653): Show |
1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.809-3754_809-3753i others(662): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467526 | |||||
| chr16:467526
|
G | GTCAGGGA others(653): Show |
1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.809-3754_809-3753i others(662): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467526 | |||||
| chr16:467526
|
G | GTCAGGGA others(719): Show |
2 | a0001c0001t0008g0065a0001c0001t0051g0064 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.809-3754_809-3753i others(728): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467526 | |||||
| chr16:467526
|
G | GTCAGGGA others(654): Show |
1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.809-3754_809-3753i others(663): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467526 | |||||
| chr16:467542
|
A | AGGGGCCT others(103): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809-3688_809-3687i others(112): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467542 | |||||
| chr16:467542
|
A | G | 20 | a0001c0001t0007g0082a0001c0001t0010g0032a0001c0001t0010g0046others(17): Show | 20 | HG01106.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.809-3753A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467542 | ||||||
| chr16:467542
|
A | T | 28 | a0001c0001t0003g0060a0001c0001t0003g0213a0001c0001t0004g0051others(25): Show | 28 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.809-3753A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467542 | ||||||
| chr16:467548
|
C | CTCAGGGA others(609): Show |
1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.809-3728_809-3727i others(618): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467548 | |||||
| chr16:467548
|
C | CTCAGGGA others(653): Show |
1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.809-3728_809-3727i others(662): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467548 | |||||
| chr16:467548
|
C | G | 4 | a0001c0002t0019g0037a0001c0002t0043g0025a0001c0006t0058g0111others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3747C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467548 | ||||||
| chr16:467560
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3735G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467560 | ||||||
| chr16:467564
|
T | G | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3731T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467564 | ||||||
| chr16:467564
|
T | TCGGACGT others(81): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3731_809-3730i others(90): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467564 | ||||||
| chr16:467564
|
T | TGGGGCCT others(565): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.809-3728_809-3727i others(574): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467564 | |||||
| chr16:467568
|
A | ACGTCAGG others(15): Show |
43 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(40): Show | 43 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.809-3710_809-3709i others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467568 | |||||
| chr16:467568
|
A | ACGTCAGG others(433): Show |
2 | a0001c0001t0011g0084a0004c0007t0022g0186 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.809-3710_809-3709i others(442): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467568 | |||||
| chr16:467568
|
A | ACGTCAGG others(169): Show |
1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.809-3688_809-3687i others(178): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467568 | |||||
| chr16:467568
|
A | ACGTCAGG others(125): Show |
1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.809-3688_809-3687i others(134): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467568 | |||||
| chr16:467568
|
A | G | 31 | a0001c0001t0003g0060a0001c0001t0003g0213a0001c0001t0004g0051others(28): Show | 31 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.809-3727A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467568 | ||||||
| chr16:467569
|
C | T | 1 | a0001c0001t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.809-3726C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467569 | ||||||
| chr16:467570
|
G | C | 4 | a0001c0001t0007g0082a0001c0001t0011g0179a0001c0001t0048g0050others(1): Show | 4 | HG02886.hp1 NA18942.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3725G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467570 | ||||||
| chr16:467584
|
G | C | 20 | a0001c0001t0003g0060a0001c0001t0003g0213a0001c0001t0004g0051others(17): Show | 20 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.809-3711G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467584 | ||||||
| chr16:467586
|
T | A | 6 | a0001c0001t0008g0148a0001c0001t0025g0021a0001c0001t0029g0020others(3): Show | 6 | HG01070.hp2 HG01109.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-3709T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467586 | ||||||
| chr16:467586
|
T | G | 44 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(41): Show | 44 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.809-3709T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467586 | ||||||
| chr16:467590
|
G | A | 3 | a0001c0001t0007g0082a0001c0001t0011g0179a0001c0002t0043g0025 | 3 | HG02886.hp1 NA19012.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.809-3705G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467590 | ||||||
| chr16:467592
|
C | CTCAGGGA others(543): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.809-3684_809-3683i others(552): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467592 | |||||
| chr16:467592
|
C | G | 52 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(49): Show | 52 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.809-3703C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467592 | ||||||
| chr16:467603
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.809-3692G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467603 | ||||||
| chr16:467608
|
T | A | 22 | a0001c0001t0003g0060a0001c0001t0003g0213a0001c0001t0004g0051others(19): Show | 22 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.809-3687T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467608 | ||||||
| chr16:467608
|
T | G | 47 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(44): Show | 47 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.809-3687T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467608 | ||||||
| chr16:467608
|
T | TGGGACGT others(37): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.809-3684_809-3683i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467608 | |||||
| chr16:467612
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3683G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467612 | ||||||
| chr16:467614
|
G | C | 21 | a0001c0001t0003g0180a0001c0001t0005g0066a0001c0001t0006g0151others(18): Show | 21 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.809-3681G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467614 | ||||||
| chr16:467614
|
GTCAGGGA others(15): Show |
G | 11 | a0001c0001t0001g0162a0001c0001t0001g0203a0001c0001t0010g0032others(8): Show | 12 | HG01069.hp1 HG01071.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-3643_809-3622d others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467614 | |||||
| chr16:467630
|
T | A | 20 | a0001c0001t0003g0060a0001c0001t0003g0213a0001c0001t0004g0051others(17): Show | 20 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.809-3665T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467630 | ||||||
| chr16:467630
|
T | G | 6 | a0001c0001t0008g0148a0001c0001t0008g0294a0001c0001t0011g0179others(3): Show | 6 | HG01070.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-3665T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467630 | ||||||
| chr16:467630
|
T | TGGGGCGT others(59): Show |
2 | a0001c0001t0011g0084a0004c0007t0022g0186 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.809-3660_809-3659i others(68): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467630 | |||||
| chr16:467634
|
G | A | 47 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(44): Show | 47 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.809-3661G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467634 | ||||||
| chr16:467636
|
C | CTCAGGGA others(81): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.809-3638_809-3637i others(90): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467636 | |||||
| chr16:467636
|
C | G | 89 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(86): Show | 89 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.809-3659C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467636 | ||||||
| chr16:467650
|
G | C | 3 | a0001c0001t0005g0066a0001c0001t0008g0068a0001c0001t0048g0050 | 3 | HG00558.hp1 NA18942.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.809-3645G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467650 | ||||||
| chr16:467650
|
G | CCTGGGGC others(59): Show |
5 | a0001c0001t0040g0083a0001c0002t0009g0081a0001c0002t0009g0269others(2): Show | 5 | HG00323.hp2 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-3646_809-3645i others(68): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467650 | ||||||
| chr16:467652
|
T | A | 2 | a0001c0001t0015g0122a0001c0014t0039g0112 | 2 | HG02895.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.809-3643T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467652 | ||||||
| chr16:467656
|
G | A | 4 | a0001c0001t0008g0148a0001c0001t0029g0020a0001c0001t0034g0208others(1): Show | 4 | HG01070.hp2 HG03669.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3639G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467656 | ||||||
| chr16:467658
|
C | G | 12 | a0001c0001t0008g0148a0001c0001t0015g0122a0001c0001t0029g0020others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-3637C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467658 | ||||||
| chr16:467674
|
A | AGGGGCCT others(147): Show |
1 | a0001c0001t0011g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.809-3616_809-3615i others(156): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467674 | |||||
| chr16:467674
|
A | T | 54 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.809-3621A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467674 | ||||||
| chr16:467680
|
G | C | 4 | a0001c0001t0008g0148a0001c0001t0011g0179a0001c0001t0029g0020others(1): Show | 4 | HG01070.hp2 HG03669.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3615G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467680 | ||||||
| chr16:467680
|
G | GTCAGGGA others(81): Show |
6 | a0001c0001t0003g0180a0001c0001t0007g0053a0001c0001t0017g0061others(3): Show | 6 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3602_809-3601i others(90): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467680 | |||||
| chr16:467680
|
G | GTCAGGGA others(81): Show |
1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.809-3600_809-3599i others(90): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467680 | |||||
| chr16:467694
|
G | C | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.809-3601G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467694 | ||||||
| chr16:467696
|
A | AGGGGCGT others(37): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.809-3572_809-3571i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467696 | |||||
| chr16:467696
|
A | G | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3599A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467696 | ||||||
| chr16:467696
|
A | T | 49 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(46): Show | 49 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.809-3599A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467696 | ||||||
| chr16:467700
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3595G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467700 | ||||||
| chr16:467701
|
C | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3594C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467701 | ||||||
| chr16:467702
|
G | C | 43 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(40): Show | 43 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.809-3593G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467702 | ||||||
| chr16:467718
|
T | A | 7 | a0001c0001t0003g0180a0001c0001t0007g0053a0001c0001t0017g0061others(4): Show | 7 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-3577T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467718 | ||||||
| chr16:467718
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.809-3577T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467718 | ||||||
| chr16:467722
|
G | A | 2 | a0001c0001t0015g0122a0001c0002t0043g0025 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.809-3573G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467722 | ||||||
| chr16:467724
|
C | CTCAGGGA others(235): Show |
1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.809-3550_809-3549i others(244): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467724 | |||||
| chr16:467724
|
C | CTCAGGGA others(455): Show |
1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-3556_809-3555i others(464): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467724 | |||||
| chr16:467724
|
C | CTCAGGGA others(169): Show |
1 | a0001c0001t0008g0063 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.809-3556_809-3555i others(178): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467724 | |||||
| chr16:467724
|
C | G | 11 | a0001c0001t0003g0180a0001c0001t0007g0053a0001c0001t0015g0122others(8): Show | 11 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.809-3571C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467724 | ||||||
| chr16:467738
|
G | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-3557G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467738 | ||||||
| chr16:467740
|
A | AGGGGCGT others(37): Show |
2 | a0001c0001t0005g0066a0001c0001t0048g0050 | 2 | HG00558.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.809-3550_809-3549i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467740 | |||||
| chr16:467740
|
A | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.809-3555A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467740 | ||||||
| chr16:467744
|
G | A | 68 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.809-3551G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467744 | ||||||
| chr16:467746
|
C | CTCAGGGA others(15): Show |
4 | a0001c0001t0003g0180a0001c0001t0005g0066a0001c0001t0028g0091others(1): Show | 4 | HG00558.hp1 HG01109.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3533_809-3512d others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467746 | |||||
| chr16:467746
|
C | CTCAGGGA others(125): Show |
1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.809-3534_809-3533i others(134): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467746 | |||||
| chr16:467746
|
C | G | 160 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.809-3549C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467746 | ||||||
| chr16:467759
|
T | A | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-3536T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467759 | ||||||
| chr16:467762
|
A | AGGGGCGT others(235): Show |
5 | a0001c0001t0007g0053a0001c0001t0017g0061a0001c0001t0017g0087others(2): Show | 5 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-3512_809-3511i others(244): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467762 | |||||
| chr16:467762
|
A | T | 6 | a0001c0001t0008g0065a0001c0001t0015g0122a0001c0001t0051g0064others(3): Show | 6 | HG02257.hp2 HG02895.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3533A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467762 | ||||||
| chr16:467766
|
G | A | 2 | a0001c0001t0008g0065a0001c0001t0051g0064 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.809-3529G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467766 | ||||||
| chr16:467768
|
G | C | 69 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.809-3527G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467768 | ||||||
| chr16:467768
|
G | GTTGGAGG others(57): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3526_809-3525i others(66): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467768 | |||||
| chr16:467784
|
T | A | 8 | a0001c0001t0007g0053a0001c0001t0008g0065a0001c0001t0017g0061others(5): Show | 8 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.809-3511T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467784 | ||||||
| chr16:467788
|
G | A | 1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.809-3507G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467788 | ||||||
| chr16:467790
|
C | G | 4 | a0001c0001t0015g0122a0001c0002t0043g0025a0001c0006t0058g0111others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3505C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467790 | ||||||
| chr16:467806
|
T | A | 4 | a0001c0001t0015g0122a0001c0001t0025g0021a0001c0012t0059g0107others(1): Show | 4 | HG02895.hp2 HG03579.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3489T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467806 | ||||||
| chr16:467810
|
A | G | 6 | a0001c0001t0015g0122a0001c0001t0025g0021a0001c0002t0043g0025others(3): Show | 6 | HG02257.hp2 HG02895.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3485A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467810 | ||||||
| chr16:467812
|
G | C | 2 | a0001c0001t0015g0122a0001c0002t0043g0025 | 2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.809-3483G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467812 | ||||||
| chr16:467828
|
A | T | 5 | a0001c0001t0007g0053a0001c0001t0017g0061a0001c0001t0017g0087others(2): Show | 5 | HG00544.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-3467A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467828 | ||||||
| chr16:467834
|
C | CTCAGGGA others(409): Show |
7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-3446_809-3445i others(418): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467834 | |||||
| chr16:467834
|
C | G | 4 | a0001c0001t0015g0122a0001c0001t0025g0021a0001c0002t0043g0025others(1): Show | 4 | HG02895.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3461C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467834 | ||||||
| chr16:467850
|
T | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.809-3445T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467850 | ||||||
| chr16:467854
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3441G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467854 | ||||||
| chr16:467856
|
C | G | 74 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.809-3439C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467856 | ||||||
| chr16:467870
|
G | A | 1 | a0001c0001t0004g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.809-3425G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467870 | ||||||
| chr16:467872
|
T | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.809-3423T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467872 | ||||||
| chr16:467876
|
A | G | 72 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.809-3419A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467876 | ||||||
| chr16:467877
|
C | A | 9 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-3418C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467877 | ||||||
| chr16:467878
|
G | C | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3417G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467878 | ||||||
| chr16:467894
|
A | AGGGAAGT others(345): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-3398_809-3397i others(354): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467894 | |||||
| chr16:467894
|
A | AGGGGCGT others(235): Show |
1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.809-3396_809-3395i others(244): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467894 | |||||
| chr16:467894
|
A | T | 67 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.809-3401A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467894 | ||||||
| chr16:467900
|
C | G | 103 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.809-3395C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467900 | ||||||
| chr16:467913
|
T | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-3382T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467913 | ||||||
| chr16:467916
|
A | AGGGAAGT others(367): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.809-3376_809-3375i others(376): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467916 | |||||
| chr16:467916
|
A | T | 67 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.809-3379A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467916 | ||||||
| chr16:467921
|
C | CCTCAGGG others(35): Show |
61 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.809-3374_809-3373i others(44): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467921 | ||||||
| chr16:467921
|
C | CGTTGGAG others(13): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.809-3372_809-3371i others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467921 | |||||
| chr16:467922
|
G | C | 6 | a0001c0001t0007g0053a0001c0001t0017g0061a0001c0001t0017g0087others(3): Show | 6 | HG00544.hp1 HG01109.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3373G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467922 | ||||||
| chr16:467922
|
G | GTCAGGGA others(191): Show |
3 | a0001c0001t0003g0180a0001c0001t0003g0213a0001c0001t0004g0054 | 3 | NA18939.hp1 NA18954.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.809-3352_809-3351i others(200): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467922 | |||||
| chr16:467922
|
G | GTCAGGGA others(213): Show |
17 | a0001c0001t0003g0060a0001c0001t0004g0051a0001c0001t0004g0055others(14): Show | 17 | HG00609.hp2 HG00673.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.809-3352_809-3351i others(222): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467922 | |||||
| chr16:467922
|
G | GTCAGGGA others(191): Show |
6 | a0001c0001t0004g0059a0001c0001t0004g0178a0001c0001t0028g0091others(3): Show | 6 | HG00323.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-3352_809-3351i others(200): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467922 | |||||
| chr16:467922
|
G | GTCAGGGA others(213): Show |
1 | a0001c0001t0004g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.809-3352_809-3351i others(222): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467922 | |||||
| chr16:467922
|
G | GTCAGGGA others(37): Show |
1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3330_809-3329i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467922 | |||||
| chr16:467938
|
A | T | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3357A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467938 | ||||||
| chr16:467942
|
G | A | 9 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-3353G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467942 | ||||||
| chr16:467943
|
C | A | 9 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-3352C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467943 | ||||||
| chr16:467943
|
C | CCTCAGGG others(147): Show |
2 | a0001c0002t0019g0037a0001c0002t0019g0285 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.809-3352_809-3351i others(156): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467943 | ||||||
| chr16:467943
|
C | CGTCAGGG others(255): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3336_809-3335i others(264): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467943 | |||||
| chr16:467944
|
G | C | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3351G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467944 | ||||||
| chr16:467960
|
T | A | 45 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(42): Show | 45 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.809-3335T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467960 | ||||||
| chr16:467960
|
T | TGGGGCCT others(389): Show |
2 | a0001c0001t0008g0065a0001c0001t0051g0064 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.809-3330_809-3329i others(398): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467960 | |||||
| chr16:467960
|
T | TGGGGCGT others(191): Show |
1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.809-3314_809-3313i others(200): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467960 | |||||
| chr16:467960
|
T | TGGGGCGT others(939): Show |
1 | a0001c0001t0011g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.809-3314_809-3313i others(948): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 467960 | |||||
| chr16:467964
|
G | A | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3331G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467964 | ||||||
| chr16:467966
|
G | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.809-3329G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467966 | ||||||
| chr16:467980
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3315G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467980 | ||||||
| chr16:467982
|
T | A | 66 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.809-3313T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467982 | ||||||
| chr16:467988
|
C | G | 4 | a0001c0001t0025g0021a0001c0006t0058g0111a0001c0008t0057g0113others(1): Show | 4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3307C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 467988 | ||||||
| chr16:468009
|
C | T | 2 | a0001c0001t0008g0068a0002c0003t0011g0102 | 2 | NA18967.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.809-3286C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468009 | ||||||
| chr16:468011
|
T | TCA | 66 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.809-3284_809-3283i others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468011 | ||||||
| chr16:468011
|
T | TCAGGGAG others(61): Show |
2 | a0001c0001t0025g0021a0001c0012t0059g0107 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.809-3284_809-3283i others(70): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468011 | ||||||
| chr16:468012
|
T | G | 68 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.809-3283T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468012 | ||||||
| chr16:468028
|
A | G | 4 | a0001c0001t0025g0021a0001c0006t0058g0111a0001c0008t0057g0113others(1): Show | 4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3267A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468028 | ||||||
| chr16:468029
|
A | C | 4 | a0001c0001t0025g0021a0001c0006t0058g0111a0001c0008t0057g0113others(1): Show | 4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3266A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468029 | ||||||
| chr16:468030
|
G | C | 2 | a0001c0001t0025g0021a0001c0012t0059g0107 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.809-3265G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468030 | ||||||
| chr16:468030
|
G | GTCAGGGA others(37): Show |
7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-3242_809-3241i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468030 | |||||
| chr16:468030
|
G | GTCAGGGA others(499): Show |
34 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(31): Show | 34 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.809-3250_809-3249i others(508): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468030 | |||||
| chr16:468030
|
G | GTCAGGGA others(719): Show |
2 | a0001c0002t0019g0037a0001c0002t0019g0285 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.809-3250_809-3249i others(728): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468030 | |||||
| chr16:468030
|
G | GTCAGGGA others(477): Show |
2 | a0001c0001t0011g0084a0004c0007t0022g0186 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.809-3250_809-3249i others(486): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468030 | |||||
| chr16:468030
|
G | GTCAGGGA others(499): Show |
1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.809-3250_809-3249i others(508): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468030 | |||||
| chr16:468046
|
A | T | 62 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.809-3249A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468046 | ||||||
| chr16:468053
|
T | TCA | 68 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.809-3242_809-3241i others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468053 | ||||||
| chr16:468053
|
T | TCAGGGAG others(237): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3242_809-3241i others(246): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468053 | ||||||
| chr16:468053
|
T | TCAGGGAG others(105): Show |
47 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(44): Show | 47 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.809-3242_809-3241i others(114): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468053 | ||||||
| chr16:468054
|
T | G | 116 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.809-3241T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468054 | ||||||
| chr16:468066
|
A | T | 3 | a0001c0001t0025g0109a0001c0006t0058g0111a0001c0008t0057g0113 | 3 | HG02257.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.809-3229A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468066 | ||||||
| chr16:468070
|
A | G | 3 | a0001c0002t0043g0025a0001c0006t0058g0111a0001c0008t0057g0113 | 3 | HG02257.hp2 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.809-3225A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468070 | ||||||
| chr16:468071
|
A | C | 4 | a0001c0001t0025g0109a0001c0002t0043g0025a0001c0006t0058g0111others(1): Show | 4 | HG02257.hp2 HG03041.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-3224A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468071 | ||||||
| chr16:468074
|
G | C | 185 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(182): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.809-3221G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468074 | ||||||
| chr16:468086
|
G | C | 1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3209G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468086 | ||||||
| chr16:468088
|
A | AGGGGCGT others(15): Show |
7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-3201_809-3180d others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468088 | |||||
| chr16:468088
|
A | T | 1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3207A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468088 | ||||||
| chr16:468089
|
G | T | 1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3206G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468089 | ||||||
| chr16:468108
|
G | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-3187G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468108 | ||||||
| chr16:468110
|
T | A | 2 | a0001c0001t0010g0194a0001c0014t0039g0112 | 2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.809-3185T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468110 | ||||||
| chr16:468110
|
T | TGGGACGT others(59): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.809-3182_809-3181i others(68): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468110 | |||||
| chr16:468110
|
T | TGGGGCCT others(15): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0165 | 2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.809-3135_809-3114d others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468110 | |||||
| chr16:468114
|
G | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3181G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468114 | ||||||
| chr16:468115
|
C | CGTCAGGG others(15): Show |
107 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.809-3180_809-3179i others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468115 | ||||||
| chr16:468116
|
C | CTCAGGGA others(77): Show |
1 | a0001c0001t0010g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.809-3158_809-3157i others(86): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468116 | |||||
| chr16:468116
|
C | G | 114 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.809-3179C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468116 | ||||||
| chr16:468128
|
G | A | 1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3167G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468128 | ||||||
| chr16:468130
|
G | C | 3 | a0001c0006t0058g0111a0001c0008t0057g0113a0001c0012t0059g0107 | 3 | HG02257.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.809-3165G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468130 | ||||||
| chr16:468132
|
A | AGGGGCCT others(363): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809-3136_809-3135i others(372): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468132 | |||||
| chr16:468132
|
A | AGGGGCGT others(15): Show |
1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3158_809-3157i others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468132 | |||||
| chr16:468132
|
A | AGGGGCGT others(57): Show |
39 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(36): Show | 39 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.809-3158_809-3157i others(66): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468132 | |||||
| chr16:468132
|
A | AGGGGCGT others(99): Show |
6 | a0001c0001t0010g0032a0001c0001t0011g0110a0001c0001t0012g0030others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3158_809-3157i others(108): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468132 | |||||
| chr16:468132
|
A | C | 1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3163A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468132 | ||||||
| chr16:468132
|
A | T | 3 | a0001c0006t0058g0111a0001c0008t0057g0113a0001c0012t0059g0107 | 3 | HG02257.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.809-3163A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468132 | ||||||
| chr16:468133
|
G | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3162G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468133 | ||||||
| chr16:468134
|
G | GGAAGTCA others(17): Show |
1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-3160_809-3159i others(26): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468134 | |||||
| chr16:468136
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.809-3159G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468136 | ||||||
| chr16:468137
|
C | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.809-3158C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468137 | ||||||
| chr16:468137
|
C | T | 55 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(52): Show | 55 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.809-3158C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468137 | ||||||
| chr16:468138
|
C | CTCAGGGA others(213): Show |
2 | a0001c0001t0008g0294a0005c0017t0037g0100 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.809-3136_809-3135i others(222): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468138 | |||||
| chr16:468138
|
C | CTCAGGGA others(213): Show |
6 | a0001c0001t0013g0027a0001c0001t0013g0028a0001c0001t0013g0029others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3136_809-3135i others(222): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468138 | |||||
| chr16:468138
|
C | G | 115 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.809-3157C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468138 | ||||||
| chr16:468152
|
G | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-3143G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468152 | ||||||
| chr16:468154
|
A | AGGGGCGT others(483): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-3136_809-3135i others(492): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468154 | |||||
| chr16:468154
|
A | AGGGGCGT others(40): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.809-3136_809-3135i others(49): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468154 | |||||
| chr16:468154
|
A | T | 3 | a0001c0001t0010g0046a0001c0008t0057g0113a0001c0012t0059g0107 | 3 | HG02257.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.809-3141A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468154 | ||||||
| chr16:468160
|
C | G | 10 | a0001c0001t0001g0193a0001c0001t0010g0194a0001c0001t0013g0026others(7): Show | 10 | HG00099.hp1 HG00099.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-3135C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468160 | ||||||
| chr16:468172
|
G | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3123G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468172 | ||||||
| chr16:468176
|
A | AAGGGCGT others(458): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.809-3119_809-3118i others(467): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468176 | ||||||
| chr16:468176
|
A | AGGGAAGT others(37): Show |
3 | a0001c0001t0001g0193a0001c0001t0010g0194a0001c0001t0013g0026 | 3 | HG00099.hp2 HG02683.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.809-3116_809-3115i others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468176 | |||||
| chr16:468176
|
A | C | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3119A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468176 | ||||||
| chr16:468182
|
G | C | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3113G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468182 | ||||||
| chr16:468196
|
G | C | 2 | a0001c0001t0025g0021a0001c0006t0058g0111 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.809-3099G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468196 | ||||||
| chr16:468196
|
G | GCTGGGGC others(65): Show |
1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.809-3098_809-3097i others(74): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468196 | |||||
| chr16:468198
|
A | AGGGGCGT others(480): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.809-3094_809-3093i others(489): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468198 | |||||
| chr16:468198
|
A | AGGGGCGT others(87): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-3094_809-3093i others(96): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468198 | |||||
| chr16:468198
|
A | T | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0006t0058g0111 | 3 | HG03041.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.809-3097A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468198 | ||||||
| chr16:468202
|
A | G | 6 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0002g0169others(3): Show | 6 | HG00099.hp1 HG02257.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3093A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468202 | ||||||
| chr16:468203
|
A | AGTCAGGG others(172): Show |
2 | a0001c0001t0008g0294a0005c0017t0037g0100 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.809-3076_809-3075i others(181): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468203 | |||||
| chr16:468203
|
A | AGTCAGGG others(285): Show |
1 | a0001c0002t0016g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.809-3076_809-3075i others(294): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468203 | |||||
| chr16:468203
|
A | AGTCAGGG others(241): Show |
1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-3076_809-3075i others(250): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468203 | |||||
| chr16:468203
|
A | C | 7 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0002g0169others(4): Show | 7 | HG00099.hp1 HG02257.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-3092A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468203 | ||||||
| chr16:468218
|
G | GCAGGGGC others(310): Show |
2 | a0001c0001t0013g0028a0001c0001t0013g0035 | 2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.809-3076_809-3075i others(319): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468218 | |||||
| chr16:468218
|
G | GCAGGGGC others(332): Show |
4 | a0001c0001t0013g0027a0001c0001t0013g0029a0001c0001t0013g0033others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-3076_809-3075i others(341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468218 | |||||
| chr16:468218
|
G | GCAGGGGC others(376): Show |
10 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0023g0036others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-3076_809-3075i others(385): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468218 | |||||
| chr16:468218
|
G | GCAGGGGC others(351): Show |
1 | a0001c0001t0018g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.809-3076_809-3075i others(360): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468218 | |||||
| chr16:468220
|
T | A | 100 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.809-3075T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468220 | ||||||
| chr16:468224
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.809-3071G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468224 | ||||||
| chr16:468225
|
C | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.809-3070C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468225 | ||||||
| chr16:468230
|
G | GGGAGGAG others(354): Show |
1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.809-3058_809-3057i others(363): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(332): Show |
1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.809-3058_809-3057i others(341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(332): Show |
3 | a0001c0001t0015g0136a0001c0002t0002g0183a0002c0003t0011g0102 | 3 | HG01192.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.809-3058_809-3057i others(341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(401): Show |
1 | a0001c0001t0003g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.809-3058_809-3057i others(410): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(401): Show |
2 | a0001c0002t0005g0070a0001c0002t0005g0075 | 2 | HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.809-3058_809-3057i others(410): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(421): Show |
1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-3058_809-3057i others(430): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(332): Show |
1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.809-3058_809-3057i others(341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(354): Show |
41 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(38): Show | 41 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.809-3058_809-3057i others(363): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(423): Show |
41 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(38): Show | 41 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.809-3058_809-3057i others(432): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(423): Show |
1 | a0001c0001t0047g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.809-3058_809-3057i others(432): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468230
|
G | GGGAGGAG others(376): Show |
1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.809-3058_809-3057i others(385): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468230 | |||||
| chr16:468237
|
G | A | 1 | a0001c0001t0003g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.809-3058G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468237 | ||||||
| chr16:468240
|
G | C | 48 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0008others(45): Show | 48 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.809-3055G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468240 | ||||||
| chr16:468240
|
G | GCAGGGGC others(376): Show |
1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.809-3054_809-3053i others(385): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468240 | |||||
| chr16:468240
|
G | GCTGGGAC others(354): Show |
2 | a0001c0002t0002g0146a0001c0002t0002g0152 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.809-3050_809-3049i others(363): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468240 | |||||
| chr16:468248
|
G | A | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.809-3047G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468248 | ||||||
| chr16:468264
|
A | T | 123 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.809-3031A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468264 | ||||||
| chr16:468268
|
A | G | 124 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(121): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-3027A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468268 | ||||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
1 | a0001c0001t0006g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.809-3004_809-3003i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(552): Show |
2 | a0001c0001t0001g0193a0001c0001t0010g0194 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(561): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(417): Show |
7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-2991_809-2990i others(426): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
1 | a0001c0001t0001g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(640): Show |
1 | a0001c0001t0001g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(649): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(596): Show |
6 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(3): Show | 6 | HG01261.hp2 NA18947.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-2991_809-2990i others(605): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
2 | a0001c0001t0001g0182a0002c0003t0018g0101 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(574): Show |
1 | a0001c0001t0011g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(583): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(596): Show |
1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(605): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(596): Show |
1 | a0001c0001t0001g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.809-2991_809-2990i others(605): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(596): Show |
2 | a0001c0001t0011g0257a0001c0001t0011g0258 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(605): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
92 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0118others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
1 | a0001c0006t0032g0270 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
2 | a0001c0001t0002g0086a0001c0001t0021g0001 | 3 | HG01069.hp1 HG01071.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(640): Show |
2 | a0001c0002t0053g0271a0001c0002t0054g0267 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(649): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(640): Show |
1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(649): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(618): Show |
2 | a0001c0001t0005g0105a0002c0003t0002g0293 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(627): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(615): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0165 | 2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.809-2991_809-2990i others(624): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | AGTCAGGG others(486): Show |
1 | a0001c0001t0013g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.809-3005_809-3004i others(495): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468269 | |||||
| chr16:468269
|
A | C | 124 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(121): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.809-3026A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468269 | ||||||
| chr16:468286
|
A | AGGGGCGT others(439): Show |
1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.809-2991_809-2990i others(448): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468286 | |||||
| chr16:468286
|
A | AGGGGCGT others(417): Show |
27 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(24): Show | 27 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.809-2991_809-2990i others(426): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468286 | |||||
| chr16:468286
|
A | AGGGGTGT others(395): Show |
3 | a0001c0001t0011g0084a0001c0001t0040g0083a0004c0007t0022g0186 | 3 | HG02976.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.809-3005_809-3004i others(404): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468286 | |||||
| chr16:468286
|
A | AGGGGTGT others(417): Show |
7 | a0001c0001t0007g0082a0001c0001t0042g0085a0001c0002t0009g0081others(4): Show | 7 | HG00323.hp2 HG01106.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-3005_809-3004i others(426): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468286 | |||||
| chr16:468286
|
A | AGGGGTGT others(417): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-3005_809-3004i others(426): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468286 | |||||
| chr16:468286
|
A | T | 6 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025others(3): Show | 6 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-3009A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468286 | ||||||
| chr16:468296
|
G | GGGAGGAG others(390): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.809-2991_809-2990i others(399): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 468296 | |||||
| chr16:468327
|
C | A | 165 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.809-2968C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468327 | ||||||
| chr16:468525
|
A | G | 64 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.809-2770A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468525 | ||||||
| chr16:468545
|
G | C | 3 | a0001c0001t0004g0088a0001c0001t0004g0090a0001c0001t0028g0091 | 3 | HG02083.hp1 NA18612.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.809-2750G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468545 | ||||||
| chr16:468689
|
T | A | 9 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(6): Show | 9 | HG01261.hp2 HG02717.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-2606T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468689 | ||||||
| chr16:468808
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-2487T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468808 | ||||||
| chr16:468828
|
G | A | 38 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.809-2467G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468828 | ||||||
| chr16:468891
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-2404C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468891 | ||||||
| chr16:468893
|
C | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-2402C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 468893 | ||||||
| chr16:469128
|
C | T | 1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.809-2167C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469128 | ||||||
| chr16:469274
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-2021C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469274 | ||||||
| chr16:469370
|
G | A | 1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.809-1925G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469370 | ||||||
| chr16:469394
|
G | T | 165 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.809-1901G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469394 | ||||||
| chr16:469399
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.809-1896A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469399 | ||||||
| chr16:469404
|
T | C | 103 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.809-1891T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469404 | ||||||
| chr16:469545
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.809-1750C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469545 | ||||||
| chr16:469632
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.809-1663C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469632 | ||||||
| chr16:469641
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.809-1654C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469641 | ||||||
| chr16:469686
|
G | A | 32 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(29): Show | 32 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.809-1609G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469686 | ||||||
| chr16:469712
|
T | C | 165 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.809-1583T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469712 | ||||||
| chr16:469725
|
A | G | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025 | 3 | NA19043.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.809-1570A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469725 | ||||||
| chr16:469788
|
G | A | 1 | a0001c0002t0054g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.809-1507G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469788 | ||||||
| chr16:469968
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-1327T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469968 | ||||||
| chr16:469989
|
C | T | 43 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0003g0213others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.809-1306C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 469989 | ||||||
| chr16:470034
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.809-1261G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470034 | ||||||
| chr16:470423
|
G | A | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.809-872G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470423 | ||||||
| chr16:470426
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.809-869C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470426 | ||||||
| chr16:470490
|
T | A | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-805T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470490 | ||||||
| chr16:470527
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.809-768G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470527 | ||||||
| chr16:470630
|
G | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.809-665G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470630 | ||||||
| chr16:470791
|
A | G | 9 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(6): Show | 9 | HG01261.hp2 HG02717.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-504A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470791 | ||||||
| chr16:470826
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.809-469G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 470826 | ||||||
| chr16:470979
|
C | CT | 62 | a0001c0001t0001g0268a0001c0001t0003g0060a0001c0001t0003g0180others(59): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.809-305dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 470979 | |||||
| chr16:470979
|
C | CTT | 85 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0002others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.809-306_809-305dup others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 470979 | |||||
| chr16:470979
|
C | CTTT | 29 | a0001c0001t0001g0140a0001c0001t0003g0125a0001c0001t0003g0133others(26): Show | 29 | HG00544.hp2 HG00609.hp1 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.809-307_809-305dup others(3): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 470979 | |||||
| chr16:471158
|
T | G | 1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.809-137T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 471158 | ||||||
| chr16:471170
|
A | C | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-125A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 471170 | ||||||
| chr16:471171
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-124G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 471171 | ||||||
| chr16:471238
|
G | T | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.809-57G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 471238 | ||||||
| chr16:471253
|
G | A | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-42G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 2/13 | chr16 | 471253 | ||||||
| chr16:471459
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+70G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 471459 | ||||||
| chr16:471473
|
C | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | HG02109.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+84C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 471473 | ||||||
| chr16:471535
|
G | A | 1 | a0001c0001t0018g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.903+146G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 471535 | ||||||
| chr16:471702
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.903+313G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 471702 | ||||||
| chr16:472139
|
C | T | 1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.903+750C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472139 | ||||||
| chr16:472209
|
T | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+820T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472209 | ||||||
| chr16:472306
|
G | A | 1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.903+917G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472306 | ||||||
| chr16:472476
|
G | A | 2 | a0001c0001t0002g0017a0001c0011t0002g0019 | 2 | NA18950.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.903+1087G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472476 | ||||||
| chr16:472552
|
T | G | 1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.903+1163T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472552 | ||||||
| chr16:472610
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+1221C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472610 | ||||||
| chr16:472671
|
C | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+1282C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472671 | ||||||
| chr16:472672
|
C | T | 82 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.903+1283C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472672 | ||||||
| chr16:472673
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+1284G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472673 | ||||||
| chr16:472726
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.903+1337T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472726 | ||||||
| chr16:472772
|
C | T | 1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.903+1383C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472772 | ||||||
| chr16:472856
|
C | T | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.903+1467C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472856 | ||||||
| chr16:472909
|
C | T | 6 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(3): Show | 6 | HG01261.hp2 NA18947.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+1520C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 472909 | ||||||
| chr16:473120
|
C | T | 56 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.903+1731C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473120 | ||||||
| chr16:473416
|
G | A | 1 | a0001c0002t0009g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.903+2027G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473416 | ||||||
| chr16:473433
|
A | G | 52 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.903+2044A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473433 | ||||||
| chr16:473610
|
AT | A | 163 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.903+2231delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 473610 | |||||
| chr16:473640
|
G | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.903+2251G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473640 | ||||||
| chr16:473747
|
T | C | 2 | a0001c0001t0006g0243a0001c0001t0012g0226 | 2 | HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.903+2358T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473747 | ||||||
| chr16:473803
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.903+2414G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473803 | ||||||
| chr16:473963
|
C | G | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.903+2574C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473963 | ||||||
| chr16:473985
|
C | T | 19 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(16): Show | 19 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.903+2596C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 473985 | ||||||
| chr16:474251
|
G | A | 1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.903+2862G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474251 | ||||||
| chr16:474297
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+2908C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474297 | ||||||
| chr16:474305
|
T | G | 59 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0268others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.903+2916T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474305 | ||||||
| chr16:474323
|
C | T | 11 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(8): Show | 11 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+2934C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474323 | ||||||
| chr16:474337
|
A | G | 3 | a0001c0002t0005g0070a0001c0002t0005g0075a0001c0002t0005g0079 | 3 | HG00323.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.903+2948A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474337 | ||||||
| chr16:474398
|
A | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+3009A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474398 | ||||||
| chr16:474446
|
T | C | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+3057T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474446 | ||||||
| chr16:474478
|
C | T | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0220others(3): Show | 6 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+3089C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474478 | ||||||
| chr16:474531
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.903+3142G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474531 | ||||||
| chr16:474531
|
G | T | 1 | a0002c0003t0005g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.903+3142G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474531 | ||||||
| chr16:474594
|
G | T | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.903+3205G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474594 | ||||||
| chr16:474612
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.903+3223G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474612 | ||||||
| chr16:474800
|
A | G | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.903+3411A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474800 | ||||||
| chr16:474961
|
CATT | C | 45 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(42): Show | 45 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.903+3573_903+3575d others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 474961 | ||||||
| chr16:475192
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+3803T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475192 | ||||||
| chr16:475293
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.903+3904C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475293 | ||||||
| chr16:475440
|
G | A | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+4051G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475440 | ||||||
| chr16:475463
|
C | G | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+4074C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475463 | ||||||
| chr16:475481
|
G | A | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+4092G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475481 | ||||||
| chr16:475519
|
T | C | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.903+4130T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475519 | ||||||
| chr16:475693
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.903+4304C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475693 | ||||||
| chr16:475699
|
C | A | 1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.903+4310C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475699 | ||||||
| chr16:475812
|
A | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(10): Show | 13 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+4423A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475812 | ||||||
| chr16:475814
|
C | G | 1 | a0001c0001t0061g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.903+4425C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475814 | ||||||
| chr16:475856
|
A | T | 7 | a0001c0001t0013g0027a0001c0001t0013g0028a0001c0001t0013g0029others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+4467A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475856 | ||||||
| chr16:475862
|
TAA | T | 7 | a0001c0001t0013g0027a0001c0001t0013g0028a0001c0001t0013g0029others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+4475_903+4476d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 475862 | |||||
| chr16:475863
|
A | T | 1 | a0001c0001t0013g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.903+4474A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475863 | ||||||
| chr16:475864
|
A | T | 1 | a0001c0001t0013g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.903+4475A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475864 | ||||||
| chr16:475865
|
A | T | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4476A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475865 | ||||||
| chr16:475868
|
G | T | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4479G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475868 | ||||||
| chr16:475879
|
T | C | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4490T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475879 | ||||||
| chr16:475888
|
A | G | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4499A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475888 | ||||||
| chr16:475894
|
T | C | 1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.903+4505T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475894 | ||||||
| chr16:475896
|
A | G | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4507A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 475896 | ||||||
| chr16:476003
|
C | T | 8 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+4614C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476003 | ||||||
| chr16:476082
|
C | T | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+4693C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476082 | ||||||
| chr16:476278
|
A | G | 1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.903+4889A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476278 | ||||||
| chr16:476377
|
G | A | 1 | a0001c0001t0056g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.903+4988G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476377 | ||||||
| chr16:476435
|
C | T | 60 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(57): Show | 60 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.903+5046C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476435 | ||||||
| chr16:476519
|
C | T | 2 | a0001c0002t0019g0037a0001c0002t0019g0285 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.903+5130C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476519 | ||||||
| chr16:476606
|
T | C | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.903+5217T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476606 | ||||||
| chr16:476694
|
T | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.903+5305T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476694 | ||||||
| chr16:476702
|
G | A | 1 | a0001c0001t0005g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.903+5313G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476702 | ||||||
| chr16:476776
|
C | CA | 6 | a0001c0001t0001g0278a0001c0001t0015g0184a0001c0001t0025g0021others(3): Show | 6 | HG01192.hp2 HG02055.hp1 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+5403dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 476776 | |||||
| chr16:476832
|
T | TGTAATCC others(13): Show |
1 | a0001c0001t0008g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.903+5445_903+5464d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 476832 | |||||
| chr16:476865
|
C | T | 82 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.903+5476C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476865 | ||||||
| chr16:476959
|
T | C | 14 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(11): Show | 14 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-5566T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476959 | ||||||
| chr16:476979
|
C | T | 1 | a0001c0001t0005g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.904-5546C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 476979 | ||||||
| chr16:477085
|
CA | C | 160 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.904-5421delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 477085 | |||||
| chr16:477085
|
CAA | C | 83 | a0001c0001t0001g0140a0001c0001t0001g0288a0001c0001t0002g0002others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.904-5422_904-5421d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 477085 | |||||
| chr16:477103
|
AATTAG | A | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(43): Show | 46 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.904-5421_904-5417d others(7): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477103 | ||||||
| chr16:477110
|
C | T | 46 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(43): Show | 46 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.904-5415C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477110 | ||||||
| chr16:477252
|
C | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.904-5273C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477252 | ||||||
| chr16:477280
|
T | C | 1 | a0001c0001t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.904-5245T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477280 | ||||||
| chr16:477334
|
C | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.904-5191C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477334 | ||||||
| chr16:477448
|
G | C | 3 | a0003c0005t0014g0022a0003c0005t0014g0023a0003c0005t0014g0024 | 3 | HG03453.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.904-5077G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477448 | ||||||
| chr16:477453
|
G | A | 1 | a0001c0001t0021g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.904-5072G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477453 | ||||||
| chr16:477457
|
C | G | 85 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.904-5068C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477457 | ||||||
| chr16:477485
|
G | A | 44 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(41): Show | 44 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.904-5040G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477485 | ||||||
| chr16:477803
|
C | T | 1 | a0001c0001t0013g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.904-4722C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477803 | ||||||
| chr16:477858
|
C | T | 1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.904-4667C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477858 | ||||||
| chr16:477961
|
A | G | 81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.904-4564A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 477961 | ||||||
| chr16:478095
|
C | T | 1 | a0001c0001t0002g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.904-4430C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 478095 | ||||||
| chr16:478195
|
C | CT | 9 | a0001c0001t0001g0206a0001c0001t0001g0259a0001c0001t0001g0288others(6): Show | 9 | HG02738.hp1 HG02897.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-4314dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 478195 | |||||
| chr16:478195
|
CT | C | 38 | a0001c0001t0001g0145a0001c0001t0003g0180a0001c0001t0010g0032others(35): Show | 38 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.904-4314delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 478195 | |||||
| chr16:478315
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.904-4210C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 478315 | ||||||
| chr16:478404
|
G | T | 1 | a0001c0001t0005g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.904-4121G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 478404 | ||||||
| chr16:478449
|
C | G | 2 | a0001c0001t0020g0247a0007c0015t0020g0199 | 2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.904-4076C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 478449 | ||||||
| chr16:478486
|
C | T | 1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904-4039C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 478486 | ||||||
| chr16:479331
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.904-3194G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 479331 | ||||||
| chr16:479448
|
G | T | 2 | a0001c0001t0003g0180a0001c0001t0003g0213 | 2 | NA18939.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.904-3077G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 479448 | ||||||
| chr16:479760
|
A | G | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.904-2765A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 479760 | ||||||
| chr16:479918
|
A | AAAC | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.904-2595_904-2593d others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 479918 | |||||
| chr16:479988
|
A | T | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-2537A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 479988 | ||||||
| chr16:480155
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.904-2370C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480155 | ||||||
| chr16:480156
|
G | C | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904-2369G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480156 | ||||||
| chr16:480157
|
C | T | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0008others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.904-2368C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480157 | ||||||
| chr16:480210
|
G | A | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904-2315G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480210 | ||||||
| chr16:480286
|
C | CAAAAA | 6 | a0001c0001t0002g0176a0001c0001t0003g0125a0001c0001t0003g0235others(3): Show | 6 | HG02572.hp2 HG02896.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-2223_904-2219d others(7): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAA | 52 | a0001c0001t0001g0140a0001c0001t0002g0008a0001c0001t0002g0010others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.904-2224_904-2219d others(8): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA | 11 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0003g0211others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.904-2225_904-2219d others(9): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0008g0294a0005c0017t0037g0100 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.904-2228_904-2219d others(12): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.904-2235_904-2219d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0015g0122a0001c0001t0041g0126 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.904-2236_904-2219d others(20): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0015g0184a0001c0001t0024g0129a0001c0001t0033g0128others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-2237_904-2219d others(21): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0015g0123a0001c0001t0024g0185 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.904-2238_904-2219d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0015g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.904-2219_904-2218i others(23): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.904-2231_904-2230i others(15): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(7): Show |
7 | a0001c0001t0003g0060a0001c0001t0003g0180a0001c0001t0004g0056others(4): Show | 7 | HG01975.hp2 HG02965.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-2231_904-2230i others(16): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(8): Show |
17 | a0001c0001t0003g0213a0001c0001t0004g0054a0001c0001t0004g0059others(14): Show | 17 | HG00544.hp1 HG00609.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.904-2231_904-2230i others(17): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(9): Show |
29 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(26): Show | 29 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.904-2231_904-2230i others(18): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
C | CAAAAAAA others(10): Show |
8 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(5): Show | 8 | HG01106.hp1 HG01109.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-2231_904-2230i others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480286
|
CA | C | 18 | a0001c0001t0001g0198a0001c0001t0001g0224a0001c0001t0001g0229others(15): Show | 18 | HG00408.hp2 HG01070.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.904-2219delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480286 | |||||
| chr16:480364
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.904-2161G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480364 | ||||||
| chr16:480386
|
A | G | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-2139A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480386 | ||||||
| chr16:480658
|
C | G | 63 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.904-1867C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480658 | ||||||
| chr16:480674
|
AT | A | 3 | a0001c0001t0015g0136a0001c0001t0041g0126a0001c0001t0056g0124 | 3 | HG02572.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.904-1846delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480674 | |||||
| chr16:480720
|
G | A | 50 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.904-1805G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480720 | ||||||
| chr16:480757
|
C | T | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-1768C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480757 | ||||||
| chr16:480776
|
GCGTGAGC others(304): Show |
G | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-1739_904-1429d others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480776 | |||||
| chr16:480815
|
A | AT | 64 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.904-1698dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 480815 | |||||
| chr16:480815
|
A | T | 1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.904-1710A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480815 | ||||||
| chr16:480967
|
A | G | 63 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.904-1558A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480967 | ||||||
| chr16:480970
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.904-1555C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 480970 | ||||||
| chr16:481056
|
G | A | 50 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(47): Show | 50 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.904-1469G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481056 | ||||||
| chr16:481060
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.904-1465C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481060 | ||||||
| chr16:481121
|
TTTAA | T | 63 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(60): Show | 63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.904-1393_904-1390d others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481121 | |||||
| chr16:481125
|
AT | A | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.904-1398delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481125 | |||||
| chr16:481243
|
G | C | 81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.904-1282G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481243 | ||||||
| chr16:481368
|
A | G | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-1157A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481368 | ||||||
| chr16:481521
|
C | A | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-1004C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481521 | ||||||
| chr16:481537
|
AGCAAGCT others(117): Show |
A | 1 | a0001c0001t0006g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.904-763_904-640del | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481537 | |||||
| chr16:481537
|
AGCAAGCT others(179): Show |
A | 4 | a0001c0001t0001g0239a0001c0001t0006g0196a0001c0001t0006g0238others(1): Show | 4 | HG01346.hp2 HG02027.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-825_904-640del | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481537 | |||||
| chr16:481687
|
G | C | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-838G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481687 | ||||||
| chr16:481749
|
G | C | 2 | a0001c0001t0015g0123a0001c0001t0015g0127 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.904-776G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481749 | ||||||
| chr16:481824
|
A | G | 2 | a0001c0001t0004g0054a0001c0001t0006g0207 | 2 | HG02132.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.904-701A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481824 | ||||||
| chr16:481830
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0006g0207 | 2 | HG02132.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.904-695A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481830 | ||||||
| chr16:481830
|
A | CGGTGCCA others(117): Show |
1 | a0001c0001t0004g0054 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.904-696_904-695ins others(124): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481830 | ||||||
| chr16:481839
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.904-686C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481839 | ||||||
| chr16:481840
|
A | G | 4 | a0001c0001t0004g0054a0001c0001t0006g0207a0001c0008t0057g0113others(1): Show | 4 | HG02132.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-685A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481840 | ||||||
| chr16:481860
|
G | A | 1 | a0001c0001t0049g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.904-665G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481860 | ||||||
| chr16:481860
|
G | GTCAGTCT others(117): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904-640_904-639ins others(124): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481860 | |||||
| chr16:481860
|
G | GTCAGTCT others(55): Show |
2 | a0001c0001t0003g0252a0001c0001t0034g0208 | 2 | NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.904-634_904-633ins others(62): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481860 | |||||
| chr16:481892
|
C | A | 95 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.904-633C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481892 | ||||||
| chr16:481892
|
C | CGGTGCCA others(55): Show |
4 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025others(1): Show | 4 | HG02109.hp1 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-479_904-418dup others(62): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481892 | |||||
| chr16:481892
|
C | CGGTGCCA others(179): Show |
1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.904-542_904-541ins others(186): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481892 | |||||
| chr16:481892
|
C | CGGTGCCA others(179): Show |
53 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.904-603_904-418dup others(186): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481892 | |||||
| chr16:481892
|
C | CGGTGCCA others(241): Show |
7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-572_904-571ins others(248): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481892 | |||||
| chr16:481909
|
G | A | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904-616G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481909 | ||||||
| chr16:481909
|
G | GGCAAGCT others(55): Show |
81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.904-604_904-603ins others(62): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 481909 | |||||
| chr16:481922
|
G | A | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-603G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481922 | ||||||
| chr16:481984
|
G | A | 29 | a0001c0001t0001g0268a0001c0001t0003g0133a0001c0001t0003g0135others(26): Show | 30 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.904-541G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 481984 | ||||||
| chr16:482046
|
G | T | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.904-479G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482046 | ||||||
| chr16:482072
|
G | A | 83 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.904-453G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482072 | ||||||
| chr16:482088
|
G | GCACCTGG others(179): Show |
1 | a0001c0001t0004g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.904-418_904-417ins others(186): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 482088 | |||||
| chr16:482108
|
A | G | 168 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.904-417A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482108 | ||||||
| chr16:482134
|
GCAGGCAG others(55): Show |
G | 1 | a0001c0002t0009g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.904-375_904-314del others(62): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 482134 | |||||
| chr16:482196
|
A | G | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.904-329A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482196 | ||||||
| chr16:482248
|
A | G | 150 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.904-277A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482248 | ||||||
| chr16:482279
|
C | G | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.904-246C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482279 | ||||||
| chr16:482305
|
C | T | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.904-220C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482305 | ||||||
| chr16:482306
|
G | A | 1 | a0001c0001t0012g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.904-219G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482306 | ||||||
| chr16:482374
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.904-151T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482374 | ||||||
| chr16:482453
|
CAGT | C | 4 | a0001c0001t0001g0268a0001c0001t0008g0265a0001c0001t0021g0001others(1): Show | 5 | HG01069.hp1 HG01071.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-71_904-69delAG others(1): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 3/13 | chr16 | 482453 | ||||||
| chr16:482968
|
CTG | C | 81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1115+235_1115+236d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 482968 | |||||
| chr16:483052
|
G | A | 52 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1115+316G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483052 | ||||||
| chr16:483121
|
G | A | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1115+385G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483121 | ||||||
| chr16:483264
|
G | A | 64 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1115+528G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483264 | ||||||
| chr16:483428
|
G | A | 1 | a0001c0001t0007g0016 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1115+692G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483428 | ||||||
| chr16:483465
|
C | G | 64 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1115+729C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483465 | ||||||
| chr16:483625
|
T | C | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1115+889T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483625 | ||||||
| chr16:483838
|
CT | C | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115+1105delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 483838 | |||||
| chr16:483882
|
T | G | 2 | a0001c0001t0015g0123a0001c0001t0015g0127 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1115+1146T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483882 | ||||||
| chr16:483918
|
G | A | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1115+1182G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 483918 | ||||||
| chr16:484033
|
A | C | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1115+1297A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484033 | ||||||
| chr16:484038
|
G | A | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1115+1302G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484038 | ||||||
| chr16:484163
|
G | T | 2 | a0001c0001t0015g0123a0001c0001t0015g0127 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1115+1427G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484163 | ||||||
| chr16:484271
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0004g0178 | 2 | NA18943.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1115+1535T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484271 | ||||||
| chr16:484356
|
A | AT | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1115+1633dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 484356 | |||||
| chr16:484500
|
C | T | 1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1115+1764C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484500 | ||||||
| chr16:484549
|
C | T | 1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1115+1813C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484549 | ||||||
| chr16:484570
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1115+1834C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484570 | ||||||
| chr16:484582
|
G | A | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1115+1846G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484582 | ||||||
| chr16:484613
|
G | A | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1115+1877G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484613 | ||||||
| chr16:484642
|
C | T | 40 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1115+1906C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484642 | ||||||
| chr16:484653
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1115+1917G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484653 | ||||||
| chr16:484674
|
C | T | 1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1115+1938C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484674 | ||||||
| chr16:484724
|
G | A | 11 | a0001c0001t0002g0086a0001c0001t0005g0105a0002c0003t0002g0093others(8): Show | 11 | HG02818.hp2 HG03130.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115+1988G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484724 | ||||||
| chr16:484747
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0004g0074others(1): Show | 4 | HG02074.hp2 NA18973.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+2011C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484747 | ||||||
| chr16:484765
|
C | T | 85 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1115+2029C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484765 | ||||||
| chr16:484849
|
C | T | 6 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(3): Show | 6 | HG00140.hp2 HG01192.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115+2113C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484849 | ||||||
| chr16:484858
|
G | A | 12 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(9): Show | 12 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1115+2122G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484858 | ||||||
| chr16:484954
|
A | G | 181 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1115+2218A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 484954 | ||||||
| chr16:485054
|
T | A | 1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1115+2318T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485054 | ||||||
| chr16:485087
|
T | C | 1 | a0001c0001t0028g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1115+2351T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485087 | ||||||
| chr16:485136
|
A | G | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1115+2400A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485136 | ||||||
| chr16:485138
|
C | A | 65 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1115+2402C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485138 | ||||||
| chr16:485160
|
C | T | 19 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(16): Show | 19 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1115+2424C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485160 | ||||||
| chr16:485193
|
G | A | 1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1115+2457G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485193 | ||||||
| chr16:485420
|
G | GT | 86 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1115+2691dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 485420 | |||||
| chr16:485598
|
A | T | 2 | a0001c0001t0015g0184a0001c0001t0024g0185 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1115+2862A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485598 | ||||||
| chr16:485610
|
A | G | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1115+2874A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485610 | ||||||
| chr16:485746
|
T | A | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1115+3010T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485746 | ||||||
| chr16:485766
|
T | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1115+3030T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 485766 | ||||||
| chr16:486090
|
G | C | 65 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1116-2761G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486090 | ||||||
| chr16:486111
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1116-2740C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486111 | ||||||
| chr16:486116
|
T | C | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1116-2735T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486116 | ||||||
| chr16:486252
|
G | T | 1 | a0001c0004t0003g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1116-2599G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486252 | ||||||
| chr16:486259
|
C | A | 86 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1116-2592C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486259 | ||||||
| chr16:486292
|
G | A | 1 | a0001c0001t0047g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1116-2559G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486292 | ||||||
| chr16:486323
|
C | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116-2528C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486323 | ||||||
| chr16:486351
|
G | A | 1 | a0001c0001t0010g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1116-2500G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486351 | ||||||
| chr16:486576
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0215 | 2 | HG01106.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1116-2275C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486576 | ||||||
| chr16:486577
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1116-2274G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486577 | ||||||
| chr16:486616
|
G | A | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1116-2235G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486616 | ||||||
| chr16:486631
|
G | A | 64 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1116-2220G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486631 | ||||||
| chr16:486653
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1116-2198C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486653 | ||||||
| chr16:486686
|
C | T | 40 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0009others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1116-2165C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486686 | ||||||
| chr16:486845
|
C | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1116-2006C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486845 | ||||||
| chr16:486945
|
C | G | 2 | a0001c0001t0007g0053a0001c0004t0003g0052 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1116-1906C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 486945 | ||||||
| chr16:487131
|
C | CT | 90 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1116-1703dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 487131 | |||||
| chr16:487131
|
CT | C | 98 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(95): Show | 99 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1116-1703delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 487131 | |||||
| chr16:487154
|
G | T | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1116-1697G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487154 | ||||||
| chr16:487221
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1116-1630C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487221 | ||||||
| chr16:487304
|
G | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1116-1547G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487304 | ||||||
| chr16:487321
|
A | G | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1116-1530A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487321 | ||||||
| chr16:487484
|
G | A | 1 | a0001c0001t0011g0257 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1116-1367G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487484 | ||||||
| chr16:487558
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1116-1293G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487558 | ||||||
| chr16:487559
|
C | T | 2 | a0001c0001t0002g0174a0001c0001t0002g0176 | 2 | HG01981.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1116-1292C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487559 | ||||||
| chr16:487562
|
G | A | 37 | a0001c0001t0001g0182a0001c0001t0001g0268a0001c0001t0002g0086others(34): Show | 38 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.1116-1289G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487562 | ||||||
| chr16:487595
|
C | T | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0002t0043g0025 | 3 | NA19043.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1116-1256C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487595 | ||||||
| chr16:487650
|
G | C | 187 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1116-1201G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487650 | ||||||
| chr16:487671
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1116-1180C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487671 | ||||||
| chr16:487810
|
G | T | 1 | a0001c0001t0049g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1116-1041G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487810 | ||||||
| chr16:487913
|
A | G | 150 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1116-938A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487913 | ||||||
| chr16:487979
|
T | C | 178 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(175): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1116-872T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 487979 | ||||||
| chr16:488023
|
AG | A | 15 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(12): Show | 15 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1116-826delG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488023 | |||||
| chr16:488094
|
A | G | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116-757A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488094 | ||||||
| chr16:488118
|
C | T | 2 | a0001c0002t0002g0255a0002c0003t0011g0102 | 2 | HG00140.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1116-733C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488118 | ||||||
| chr16:488119
|
G | A | 62 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(59): Show | 62 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1116-732G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488119 | ||||||
| chr16:488234
|
G | C | 1 | a0001c0001t0002g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1116-617G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488234 | ||||||
| chr16:488240
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1116-611C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488240 | ||||||
| chr16:488279
|
T | C | 206 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(203): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1116-572T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488279 | ||||||
| chr16:488331
|
T | G | 86 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1116-520T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488331 | ||||||
| chr16:488401
|
GATTT | G | 3 | a0001c0001t0013g0026a0001c0001t0013g0028a0001c0001t0013g0035 | 3 | HG02257.hp1 HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1116-437_1116-434d others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488401 | |||||
| chr16:488408
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1116-443T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488408 | ||||||
| chr16:488414
|
A | T | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0015g0039others(11): Show | 14 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1116-437A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488414 | ||||||
| chr16:488414
|
AT | A | 85 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1116-425delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488414 | |||||
| chr16:488418
|
T | A | 20 | a0001c0001t0001g0182a0001c0001t0001g0286a0001c0001t0001g0287others(17): Show | 21 | HG00544.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1116-433T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488418 | ||||||
| chr16:488419
|
T | A | 1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1116-432T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488419 | ||||||
| chr16:488565
|
T | C | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(148): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1116-286T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488565 | ||||||
| chr16:488585
|
G | GT | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116-260dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488585 | |||||
| chr16:488632
|
C | T | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1116-219C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488632 | ||||||
| chr16:488711
|
C | CT | 8 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(5): Show | 8 | HG01261.hp2 HG02257.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116-125dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488711 | |||||
| chr16:488711
|
C | CTT | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1116-126_1116-125d others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 488711 | |||||
| chr16:488720
|
T | TC | 66 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(63): Show | 66 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1116-131_1116-130i others(3): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488720 | ||||||
| chr16:488790
|
C | T | 12 | a0001c0001t0015g0039a0001c0001t0018g0043a0001c0001t0018g0044others(9): Show | 12 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116-61C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 4/13 | chr16 | 488790 | ||||||
| chr16:489047
|
G | A | 1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1265+47G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489047 | ||||||
| chr16:489088
|
T | TAA | 189 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(186): Show | 190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1265+88_1265+89ins others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489088 | ||||||
| chr16:489093
|
G | C | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1265+93G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489093 | ||||||
| chr16:489140
|
C | A | 176 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(173): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1265+140C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489140 | ||||||
| chr16:489266
|
C | T | 1 | a0001c0002t0054g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1265+266C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489266 | ||||||
| chr16:489429
|
A | G | 148 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1265+429A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489429 | ||||||
| chr16:489513
|
T | C | 3 | a0001c0001t0010g0217a0001c0001t0012g0189a0001c0001t0012g0280 | 3 | HG01074.hp1 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1265+513T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489513 | ||||||
| chr16:489527
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1265+527C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489527 | ||||||
| chr16:489547
|
G | C | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1265+547G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489547 | ||||||
| chr16:489578
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0014g0177 | 3 | HG01981.hp2 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1265+578G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489578 | ||||||
| chr16:489616
|
G | T | 1 | a0002c0003t0018g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1265+616G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489616 | ||||||
| chr16:489642
|
T | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+642T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489642 | ||||||
| chr16:489649
|
T | TAGGTTGT others(5): Show |
4 | a0001c0001t0004g0088a0001c0001t0004g0089a0001c0001t0004g0090others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265+651_1265+662d others(14): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 489649 | |||||
| chr16:489771
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1265+771T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489771 | ||||||
| chr16:489780
|
G | GGCTGTCC others(5): Show |
147 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1265+784_1265+785i others(14): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 489780 | |||||
| chr16:489793
|
G | A | 1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1265+793G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489793 | ||||||
| chr16:489813
|
T | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1265+813T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489813 | ||||||
| chr16:489882
|
A | G | 149 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1265+882A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489882 | ||||||
| chr16:489902
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1265+902G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 489902 | ||||||
| chr16:490137
|
T | C | 180 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(177): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1265+1137T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490137 | ||||||
| chr16:490221
|
G | A | 62 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1265+1221G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490221 | ||||||
| chr16:490223
|
C | T | 1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1265+1223C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490223 | ||||||
| chr16:490258
|
G | C | 64 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1265+1258G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490258 | ||||||
| chr16:490343
|
T | G | 150 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0140others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1265+1343T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490343 | ||||||
| chr16:490409
|
C | G | 5 | a0001c0001t0001g0239a0001c0001t0006g0196a0001c0001t0006g0207others(2): Show | 5 | HG01346.hp2 HG02027.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265+1409C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490409 | ||||||
| chr16:490421
|
G | T | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1265+1421G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490421 | ||||||
| chr16:490468
|
T | C | 76 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(73): Show | 76 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1265+1468T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490468 | ||||||
| chr16:490500
|
G | A | 84 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1265+1500G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490500 | ||||||
| chr16:490515
|
T | C | 49 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1265+1515T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490515 | ||||||
| chr16:490575
|
G | T | 2 | a0001c0006t0058g0111a0001c0008t0057g0113 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1265+1575G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490575 | ||||||
| chr16:490748
|
A | G | 1 | a0001c0001t0017g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1265+1748A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490748 | ||||||
| chr16:490877
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+1877C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490877 | ||||||
| chr16:490938
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1265+1938C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 490938 | ||||||
| chr16:491020
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1265+2020C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491020 | ||||||
| chr16:491067
|
C | T | 9 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1265+2067C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491067 | ||||||
| chr16:491068
|
G | T | 3 | a0001c0001t0008g0294a0004c0007t0022g0067a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1265+2068G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491068 | ||||||
| chr16:491082
|
A | G | 9 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1265+2082A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491082 | ||||||
| chr16:491091
|
C | T | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265+2091C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491091 | ||||||
| chr16:491107
|
C | A | 1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1265+2107C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491107 | ||||||
| chr16:491113
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+2113C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491113 | ||||||
| chr16:491114
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1265+2114G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491114 | ||||||
| chr16:491149
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1265+2149C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491149 | ||||||
| chr16:491251
|
TGATCTTG others(24): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1265+2252_1265+228 others(35): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491251 | ||||||
| chr16:491353
|
C | T | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265+2353C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491353 | ||||||
| chr16:491358
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1265+2358C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491358 | ||||||
| chr16:491380
|
C | T | 9 | a0001c0002t0009g0254a0001c0002t0009g0274a0001c0002t0009g0275others(6): Show | 9 | HG01261.hp2 HG02109.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1265+2380C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491380 | ||||||
| chr16:491493
|
T | C | 21 | a0001c0001t0001g0266a0001c0001t0010g0188a0001c0001t0013g0026others(18): Show | 21 | HG00738.hp2 HG01261.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1265+2493T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491493 | ||||||
| chr16:491598
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1265+2598A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491598 | ||||||
| chr16:491671
|
A | T | 85 | a0001c0001t0001g0140a0001c0001t0001g0268a0001c0001t0002g0002others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1265+2671A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491671 | ||||||
| chr16:491679
|
C | T | 81 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1265+2679C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491679 | ||||||
| chr16:491702
|
C | T | 26 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0003g0125others(23): Show | 26 | HG00544.hp2 HG00609.hp1 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.1265+2702C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491702 | ||||||
| chr16:491703
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1265+2703T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491703 | ||||||
| chr16:491752
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1265+2752A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491752 | ||||||
| chr16:491773
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0265a0001c0001t0021g0001others(3): Show | 7 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1265+2773G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491773 | ||||||
| chr16:491807
|
C | T | 1 | a0001c0001t0021g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1265+2807C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491807 | ||||||
| chr16:491818
|
C | T | 2 | a0004c0007t0022g0067a0005c0017t0037g0100 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1265+2818C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491818 | ||||||
| chr16:491821
|
T | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1265+2821T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491821 | ||||||
| chr16:491823
|
G | A | 1 | a0001c0002t0030g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1265+2823G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491823 | ||||||
| chr16:491873
|
C | T | 5 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265+2873C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491873 | ||||||
| chr16:491913
|
A | T | 1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1265+2913A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491913 | ||||||
| chr16:491972
|
C | T | 3 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0104 | 3 | HG02630.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1265+2972C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 491972 | ||||||
| chr16:492029
|
C | T | 289 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(286): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1265+3029C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492029 | ||||||
| chr16:492041
|
G | A | 1 | a0001c0001t0010g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1265+3041G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492041 | ||||||
| chr16:492047
|
A | C | 102 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0119others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1265+3047A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492047 | ||||||
| chr16:492070
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1265+3070T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492070 | ||||||
| chr16:492107
|
C | G | 1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1265+3107C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492107 | ||||||
| chr16:492111
|
C | T | 1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1265+3111C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492111 | ||||||
| chr16:492130
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1265+3130C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492130 | ||||||
| chr16:492148
|
G | A | 60 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1265+3148G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492148 | ||||||
| chr16:492258
|
A | C | 135 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0159others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1265+3258A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492258 | ||||||
| chr16:492277
|
G | A | 1 | a0002c0003t0005g0099 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1265+3277G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492277 | ||||||
| chr16:492289
|
T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1265+3289T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492289 | ||||||
| chr16:492296
|
C | T | 1 | a0001c0001t0012g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1265+3296C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492296 | ||||||
| chr16:492356
|
A | AGGCCCCT others(519): Show |
1 | a0001c0001t0006g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(530): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492356 | |||||
| chr16:492356
|
A | AGGCCCCT others(644): Show |
1 | a0001c0001t0005g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(655): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492356 | |||||
| chr16:492357
|
G | GGCCCCTC others(1187): Show |
1 | a0001c0001t0004g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(1198): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492357 | |||||
| chr16:492357
|
G | GGCCCCTC others(516): Show |
1 | a0001c0001t0001g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(527): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492357 | |||||
| chr16:492357
|
G | GGCCCCTC others(486): Show |
1 | a0001c0001t0012g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(497): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492357 | |||||
| chr16:492358
|
G | GCCCCTCC others(23): Show |
1 | a0001c0004t0008g0172 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1265+3358_1265+335 others(34): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492358 | ||||||
| chr16:492358
|
G | GGCCCTCC others(547): Show |
1 | a0001c0002t0044g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(558): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492358 | |||||
| chr16:492358
|
G | GGCCCTCC others(304): Show |
1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(315): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492358 | |||||
| chr16:492359
|
G | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0223others(9): Show | 12 | HG00438.hp1 HG02135.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.1265+3359G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GC | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0029others(4): Show | 7 | HG01261.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265+3359_1265+336 others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GCCCTCCC others(972): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(983): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GCCCTCCC others(525): Show |
1 | a0003c0005t0014g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(536): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GCCCTCCC others(805): Show |
1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(816): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GCTCTCCC others(1235): Show |
1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(1246): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492359
|
G | GCTCTCCC others(614): Show |
1 | a0001c0001t0023g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1265+3359_1265+336 others(625): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492359 | ||||||
| chr16:492360
|
T | C | 28 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0182others(25): Show | 28 | HG00438.hp1 HG01070.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1265+3360T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492360 | ||||||
| chr16:492360
|
T | TCCTCCCG others(487): Show |
1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(498): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(829): Show |
1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(840): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(1106): Show |
1 | a0001c0001t0010g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(1117): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(726): Show |
1 | a0001c0001t0010g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(737): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(456): Show |
1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(467): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(798): Show |
1 | a0001c0001t0010g0004 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(809): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(859): Show |
1 | a0001c0002t0002g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(870): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(2124): Show |
1 | a0001c0001t0001g0279 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(2135): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(759): Show |
1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(770): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(1036): Show |
1 | a0001c0002t0009g0275 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(1047): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(1106): Show |
1 | a0001c0001t0002g0015 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(1117): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(363): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0181 | 2 | NA18944.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1265+3361_1265+336 others(374): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(394): Show |
1 | a0001c0001t0001g0160 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(405): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(332): Show |
1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(343): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(425): Show |
1 | a0001c0001t0001g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(436): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(873): Show |
1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(884): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(941): Show |
1 | a0001c0002t0009g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(952): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(609): Show |
1 | a0001c0001t0005g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(620): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(3604): Show |
1 | a0001c0001t0012g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(3615): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(363): Show |
1 | a0001c0001t0001g0145 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(374): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(332): Show |
1 | a0001c0001t0001g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(343): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(1140): Show |
1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(1151): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(644): Show |
1 | a0001c0001t0023g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(655): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(86): Show |
1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(97): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(2534): Show |
1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(2545): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(864): Show |
1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(875): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCCTCCCG others(669): Show |
1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1265+3361_1265+336 others(680): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCTTCCCG others(1715): Show |
1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(1726): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCTTCCCG others(670): Show |
1 | a0004c0007t0022g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(681): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCTTCCCG others(670): Show |
1 | a0001c0001t0001g0291 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(681): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492360
|
T | TCTTCCCG others(672): Show |
2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1265+3382_1265+338 others(683): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492360 | |||||
| chr16:492362
|
T | C | 100 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0119others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1265+3362T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492362 | ||||||
| chr16:492362
|
T | TCCCGGGG others(997): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1265+3362_1265+336 others(1008): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492362 | ||||||
| chr16:492362
|
T | TTCCCGGG others(671): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1265+3382_1265+338 others(682): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492362 | |||||
| chr16:492362
|
T | TTCCCGGG others(763): Show |
1 | a0001c0001t0001g0288 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(774): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492362 | |||||
| chr16:492362
|
T | TTCCCGGG others(731): Show |
1 | a0001c0001t0001g0289 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(742): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492362 | |||||
| chr16:492362
|
TTCCCGGG others(147): Show |
T | 1 | a0001c0001t0017g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1265+3383_1265+353 others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492362 | |||||
| chr16:492363
|
T | C | 37 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0160others(34): Show | 37 | HG00423.hp2 HG01261.hp1 HG01261.hp2 others(34): Show |
intron_variant | MODIFIER | c.1265+3363T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492363 | ||||||
| chr16:492363
|
T | TCCCCGGG others(901): Show |
1 | a0001c0001t0041g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1265+3366_1265+336 others(912): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(1013): Show |
1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1265+3392_1265+339 others(1024): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(921): Show |
1 | a0001c0002t0038g0038 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(932): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(426): Show |
1 | a0001c0001t0006g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(437): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(613): Show |
1 | a0001c0001t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(624): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(302): Show |
1 | a0001c0001t0001g0218 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(313): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(459): Show |
1 | a0001c0001t0001g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(470): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(54): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(65): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(1012): Show |
1 | a0001c0001t0061g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(1023): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(480): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(491): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(301): Show |
1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(312): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(668): Show |
1 | a0001c0001t0001g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(679): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(487): Show |
1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(498): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(1246): Show |
1 | a0001c0001t0012g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(1257): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(738): Show |
1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(749): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(489): Show |
1 | a0001c0001t0002g0176 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(500): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(393): Show |
1 | a0001c0001t0055g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(404): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(551): Show |
1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(562): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGA others(586): Show |
1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(597): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGG others(1055): Show |
1 | a0001c0001t0001g0239 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1265+3369_1265+337 others(1066): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGG others(891): Show |
1 | a0001c0002t0009g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1265+3369_1265+337 others(902): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGG others(423): Show |
1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1265+3369_1265+337 others(434): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492363
|
T | TCCCGGGG others(394): Show |
1 | a0001c0002t0002g0121 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1265+3369_1265+337 others(405): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492363 | |||||
| chr16:492366
|
C | CGGGAGAC others(459): Show |
1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(470): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492366 | |||||
| chr16:492366
|
C | CGGGAGAC others(979): Show |
1 | a0003c0005t0014g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(990): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492366 | |||||
| chr16:492366
|
C | CGGGAGAC others(1167): Show |
1 | a0001c0004t0003g0175 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1265+3382_1265+338 others(1178): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492366 | |||||
| chr16:492366
|
C | CGGGGGAC others(336): Show |
1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1265+3369_1265+337 others(347): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492366 | |||||
| chr16:492370
|
A | G | 9 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0003g0235others(6): Show | 9 | HG01496.hp1 HG02257.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1265+3370A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492370 | ||||||
| chr16:492383
|
C | CCCAGAGC others(733): Show |
1 | a0001c0001t0001g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(744): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492383 | |||||
| chr16:492383
|
C | CCCAGAGC others(212): Show |
1 | a0001c0001t0060g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(223): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492383 | |||||
| chr16:492383
|
C | T | 36 | a0001c0001t0001g0118a0001c0001t0001g0140a0001c0001t0001g0161others(33): Show | 36 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1265+3383C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492383 | ||||||
| chr16:492387
|
G | GGGCCCTC others(607): Show |
1 | a0001c0001t0049g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(618): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492387 | ||||||
| chr16:492387
|
G | GGGCCCTT others(362): Show |
1 | a0001c0001t0001g0251 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1265+3387_1265+338 others(373): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492387 | ||||||
| chr16:492388
|
A | AGCCCCCC others(1246): Show |
1 | a0001c0001t0012g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1265+3392_1265+339 others(1257): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCCCC others(702): Show |
1 | a0003c0005t0014g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1265+3392_1265+339 others(713): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCCCC others(519): Show |
1 | a0001c0001t0021g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1265+3392_1265+339 others(530): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(673): Show |
1 | a0001c0001t0002g0017 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(684): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(642): Show |
1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(653): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(453): Show |
1 | a0001c0001t0001g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(464): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(515): Show |
1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1265+3444_1265+344 others(526): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(548): Show |
1 | a0001c0001t0001g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(559): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(425): Show |
1 | a0001c0001t0008g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(436): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(452): Show |
1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(463): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(863): Show |
1 | a0001c0004t0003g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(874): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1315): Show |
1 | a0001c0001t0017g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(1326): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1051): Show |
1 | a0001c0001t0027g0163 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(1062): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1407): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1418): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(332): Show |
1 | a0001c0001t0003g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(343): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1183): Show |
1 | a0001c0001t0015g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1194): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1535): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1546): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(425): Show |
1 | a0001c0001t0003g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(436): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(733): Show |
1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(744): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(332): Show |
1 | a0001c0002t0002g0255 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(343): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(357): Show |
1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(368): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1278): Show |
1 | a0001c0001t0015g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1289): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(827): Show |
1 | a0002c0003t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(838): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(363): Show |
1 | a0001c0001t0006g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(374): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(672): Show |
1 | a0001c0011t0002g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(683): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(640): Show |
1 | a0001c0002t0016g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(651): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(426): Show |
1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(437): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(643): Show |
1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(654): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(736): Show |
1 | a0001c0001t0016g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(747): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(860): Show |
1 | a0001c0002t0002g0153 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(871): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(673): Show |
2 | a0001c0002t0002g0146a0001c0002t0002g0152 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1265+3396_1265+339 others(684): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(301): Show |
1 | a0001c0001t0006g0227 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(312): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(117): Show |
1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(128): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(818): Show |
1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(829): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(302): Show |
1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(313): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1735): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1746): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(577): Show |
1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(588): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1724): Show |
1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1735): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1027): Show |
1 | a0001c0001t0010g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1038): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1168): Show |
1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1179): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTCC others(1604): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1615): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTTC others(2276): Show |
1 | a0001c0001t0011g0257 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(2287): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTTC others(1090): Show |
1 | a0001c0001t0010g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(1101): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTTC others(1216): Show |
1 | a0001c0001t0012g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(1227): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTTC others(519): Show |
1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(530): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | AGCCCTTC others(1944): Show |
1 | a0001c0001t0011g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(1955): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492388 | |||||
| chr16:492388
|
A | G | 116 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0144others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1265+3388A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492388 | ||||||
| chr16:492389
|
G | GCCCTCCC others(2423): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(2434): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492389 | |||||
| chr16:492392
|
C | CT | 5 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0029others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1265+3393dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492392 | |||||
| chr16:492392
|
C | CTTCCCGG others(3316): Show |
1 | a0001c0001t0013g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(3327): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492392 | |||||
| chr16:492393
|
T | TCCCGGGA others(3061): Show |
1 | a0001c0001t0003g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(3072): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492393 | |||||
| chr16:492393
|
T | TCCCGGGA others(973): Show |
1 | a0001c0002t0005g0079 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(984): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492393 | |||||
| chr16:492393
|
T | TTCCCGGG others(1750): Show |
1 | a0001c0001t0024g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(1761): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492393 | ||||||
| chr16:492393
|
T | TTCCCGGG others(2070): Show |
1 | a0001c0001t0003g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(2081): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492393 | ||||||
| chr16:492393
|
T | TTCCCGGG others(1588): Show |
1 | a0002c0003t0007g0095 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(1599): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492393 | ||||||
| chr16:492393
|
T | TTCCCGGG others(958): Show |
1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(969): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492393 | ||||||
| chr16:492393
|
T | TTCCCGGG others(2229): Show |
1 | a0002c0003t0007g0096 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1265+3393_1265+339 others(2240): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492393 | ||||||
| chr16:492393
|
TC | T | 25 | a0001c0001t0001g0198a0001c0001t0001g0223a0001c0001t0001g0228others(22): Show | 25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1265+3397delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492393 | |||||
| chr16:492394
|
C | CCCCGGGA others(461): Show |
1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(472): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCCGGGA others(298): Show |
1 | a0001c0001t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(309): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCCGGGA others(741): Show |
1 | a0001c0001t0001g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(752): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCCGGGA others(637): Show |
1 | a0001c0001t0001g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(648): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCCGGGA others(425): Show |
1 | a0001c0001t0050g0168 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(436): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(427): Show |
1 | a0001c0001t0001g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(438): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(1138): Show |
1 | a0001c0001t0051g0064 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1149): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(490): Show |
1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(501): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(2276): Show |
1 | a0001c0001t0011g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(2287): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(114): Show |
1 | a0001c0001t0010g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(125): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(1572): Show |
1 | a0001c0001t0018g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1583): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(1162): Show |
1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1173): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(2344): Show |
1 | a0001c0001t0011g0258 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(2355): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(115): Show |
1 | a0001c0001t0015g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(126): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(1442): Show |
1 | a0001c0001t0010g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(1453): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(486): Show |
1 | a0001c0001t0025g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(497): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGAG others(548): Show |
1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(559): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | CCCGGGGG others(578): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1265+3396_1265+339 others(589): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492394
|
C | T | 36 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0162others(33): Show | 36 | HG00408.hp2 HG00738.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1265+3394C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492394 | ||||||
| chr16:492394
|
CCCCGGGA others(116): Show |
C | 1 | a0001c0001t0002g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1265+3414_1265+353 others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492394 | |||||
| chr16:492397
|
C | CG | 10 | a0001c0001t0002g0002a0001c0001t0003g0125a0001c0001t0003g0210others(7): Show | 10 | HG02027.hp2 HG02129.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1265+3400dupG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | CGGGAGAC others(741): Show |
1 | a0001c0001t0010g0233 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(752): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | CGGGAGAC others(801): Show |
1 | a0001c0001t0001g0263 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(812): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | CGGGAGAC others(886): Show |
1 | a0001c0001t0007g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1265+3418_1265+341 others(897): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | CGGGAGAC others(1142): Show |
1 | a0001c0001t0007g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(1153): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | CGGGAGAC others(561): Show |
1 | a0001c0001t0003g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1265+3413_1265+341 others(572): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492397 | |||||
| chr16:492397
|
C | G | 12 | a0001c0001t0003g0135a0001c0001t0003g0209a0001c0001t0013g0026others(9): Show | 12 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1265+3397C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492397 | ||||||
| chr16:492401
|
A | G | 1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1265+3401A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492401 | ||||||
| chr16:492404
|
C | T | 3 | a0001c0001t0014g0143a0001c0002t0005g0070a0001c0002t0005g0075 | 3 | HG01175.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1265+3404C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492404 | ||||||
| chr16:492414
|
C | T | 17 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0286others(14): Show | 17 | HG00544.hp1 HG00642.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1265+3414C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492414 | ||||||
| chr16:492419
|
G | A | 58 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0160others(55): Show | 58 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1265+3419G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492419 | ||||||
| chr16:492419
|
G | GGCCCTCC others(210): Show |
1 | a0001c0001t0001g0230 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(221): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492419 | |||||
| chr16:492419
|
G | GGCCCTCC others(738): Show |
1 | a0001c0001t0020g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(749): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492419 | |||||
| chr16:492419
|
G | GGCCCTCC others(611): Show |
1 | a0001c0001t0003g0192 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1265+3444_1265+344 others(622): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492419 | |||||
| chr16:492421
|
C | T | 1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1265+3421C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492421 | ||||||
| chr16:492423
|
C | CT | 16 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0286others(13): Show | 16 | HG01074.hp1 HG02257.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1265+3424dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492423 | |||||
| chr16:492423
|
C | CTCCCGGG others(919): Show |
1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1265+3427_1265+342 others(930): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492423 | |||||
| chr16:492423
|
C | CTCCCGGG others(841): Show |
1 | a0001c0001t0001g0165 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1265+3427_1265+342 others(852): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492423 | |||||
| chr16:492424
|
T | C | 2 | a0001c0001t0033g0128a0001c0001t0040g0083 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1265+3424T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492424
|
T | TTCCCGGG others(366): Show |
1 | a0001c0001t0004g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(377): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492424
|
T | TTCCCGGG others(118): Show |
1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(129): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492424
|
T | TTCCCGGG others(952): Show |
1 | a0001c0001t0008g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(963): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492424
|
T | TTCCCGGG others(305): Show |
1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1265+3424_1265+342 others(316): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492424
|
TC | T | 6 | a0001c0001t0001g0215a0001c0002t0009g0081a0001c0002t0019g0037others(3): Show | 6 | HG00323.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1265+3428delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492424 | |||||
| chr16:492424
|
TCCCCGGG others(85): Show |
T | 2 | a0001c0001t0002g0005a0001c0001t0012g0189 | 2 | HG01074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1265+3425_1265+351 others(96): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492424 | ||||||
| chr16:492425
|
C | CCCCGGAG others(175): Show |
1 | a0001c0001t0006g0243 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1265+3430_1265+343 others(186): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492425 | |||||
| chr16:492425
|
C | CCCCGGGG others(670): Show |
1 | a0001c0001t0006g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1265+3431_1265+343 others(681): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492425 | |||||
| chr16:492425
|
C | CCCGGGAG others(479): Show |
1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1265+3427_1265+342 others(490): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492425 | |||||
| chr16:492425
|
C | T | 44 | a0001c0001t0001g0206a0001c0001t0001g0263a0001c0001t0001g0266others(41): Show | 44 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1265+3425C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492425 | ||||||
| chr16:492428
|
C | CG | 23 | a0001c0001t0002g0002a0001c0001t0003g0125a0001c0001t0003g0135others(20): Show | 23 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1265+3431dupG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | CGGGAGAC others(581): Show |
1 | a0001c0001t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1265+3449_1265+345 others(592): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | CGGGAGAC others(2900): Show |
1 | a0001c0001t0003g0133 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1265+3449_1265+345 others(2911): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | CGGGAGAC others(804): Show |
1 | a0001c0001t0001g0115 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(815): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | CGGGAGAC others(986): Show |
1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1265+3444_1265+344 others(997): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | CGGGAGAC others(727): Show |
1 | a0001c0001t0007g0237 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1265+3444_1265+344 others(738): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492428 | |||||
| chr16:492428
|
C | G | 20 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0165others(17): Show | 20 | HG01074.hp1 HG02080.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.1265+3428C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492428 | ||||||
| chr16:492432
|
A | G | 1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1265+3432A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492432 | ||||||
| chr16:492445
|
C | CCCAGGGC others(681): Show |
1 | a0001c0001t0001g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(692): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492445 | |||||
| chr16:492445
|
C | T | 34 | a0001c0001t0001g0182a0001c0001t0001g0206a0001c0001t0001g0286others(31): Show | 34 | HG00544.hp1 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1265+3445C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492445 | ||||||
| chr16:492450
|
G | A | 29 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0161others(26): Show | 29 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1265+3450G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492450 | ||||||
| chr16:492454
|
CT | C | 65 | a0001c0001t0001g0119a0001c0001t0001g0140a0001c0001t0001g0182others(62): Show | 66 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1265+3456delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492454 | |||||
| chr16:492455
|
T | C | 2 | a0001c0001t0025g0021a0001c0001t0042g0085 | 2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1265+3455T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(980): Show |
1 | a0001c0001t0010g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(991): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(892): Show |
1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(903): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(208): Show |
1 | a0001c0002t0002g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(219): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(581): Show |
1 | a0001c0002t0002g0167 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(592): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(705): Show |
1 | a0001c0001t0002g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(716): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(767): Show |
1 | a0001c0002t0002g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(778): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(860): Show |
3 | a0001c0001t0006g0207a0001c0002t0002g0250a0001c0006t0032g0270 | 3 | HG01261.hp1 HG02132.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1265+3455_1265+345 others(871): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(1046): Show |
1 | a0001c0002t0030g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(1057): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(1077): Show |
1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(1088): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(983): Show |
1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(994): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(950): Show |
1 | a0001c0002t0016g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(961): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(392): Show |
1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(403): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(733): Show |
1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(744): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCCGGG others(1013): Show |
1 | a0001c0001t0001g0198 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(1024): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCGGGA others(52): Show |
1 | a0001c0001t0012g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(63): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCGGGA others(921): Show |
1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(932): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCGGGA others(1075): Show |
1 | a0001c0002t0002g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(1086): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCGGGA others(578): Show |
1 | a0001c0001t0007g0016 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(589): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
T | TCCCGGGA others(331): Show |
1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1265+3455_1265+345 others(342): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492455
|
TTC | T | 3 | a0001c0001t0002g0086a0001c0002t0009g0081a0001c0013t0052g0069 | 3 | HG02145.hp2 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1265+3456_1265+345 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492455 | ||||||
| chr16:492456
|
T | C | 54 | a0001c0001t0001g0228a0001c0001t0001g0246a0001c0001t0001g0268others(51): Show | 54 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1265+3456T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492456 | ||||||
| chr16:492456
|
T | TCCGGGGA others(980): Show |
1 | a0001c0001t0004g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1265+3458_1265+345 others(991): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492456 | |||||
| chr16:492457
|
C | CCGGGAGA others(828): Show |
1 | a0001c0001t0001g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1265+3458_1265+345 others(839): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492457 | |||||
| chr16:492457
|
C | CCGGGAGA others(1476): Show |
1 | a0001c0001t0004g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1265+3458_1265+345 others(1487): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492457 | |||||
| chr16:492457
|
C | CCGGGAGA others(142): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1265+3458_1265+345 others(153): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492457 | |||||
| chr16:492459
|
CG | C | 32 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0004g0018others(29): Show | 32 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1265+3463delG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492459 | |||||
| chr16:492460
|
G | C | 94 | a0001c0001t0001g0119a0001c0001t0001g0140a0001c0001t0001g0161others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1265+3460G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492460 | ||||||
| chr16:492460
|
G | GGGAGACC others(2093): Show |
1 | a0001c0001t0004g0088 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2104): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2092): Show |
1 | a0001c0001t0004g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2103): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(3062): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(3073): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(801): Show |
1 | a0001c0001t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(812): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2246): Show |
1 | a0001c0001t0028g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2257): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1406): Show |
1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1417): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(173): Show |
1 | a0001c0001t0041g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(184): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2531): Show |
1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2542): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(393): Show |
1 | a0001c0001t0001g0278 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(404): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2404): Show |
1 | a0001c0001t0004g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2415): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2280): Show |
1 | a0001c0001t0004g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2291): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(209): Show |
1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(220): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(426): Show |
1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(437): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(3174): Show |
1 | a0001c0001t0004g0059 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(3185): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(513): Show |
1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(524): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1068): Show |
1 | a0001c0001t0014g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1079): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2090): Show |
1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2101): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(23): Show |
1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(34): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1353): Show |
1 | a0001c0001t0003g0060 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1364): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1161): Show |
1 | a0001c0002t0005g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1172): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(3130): Show |
1 | a0006c0010t0005g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(3141): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1764): Show |
1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1775): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(982): Show |
1 | a0001c0001t0001g0228 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(993): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(203): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(214): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(511): Show |
1 | a0001c0001t0056g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(522): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1536): Show |
1 | a0001c0001t0004g0054 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1547): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(330): Show |
1 | a0001c0002t0005g0079 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1421): Show |
1 | a0001c0001t0008g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1432): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1131): Show |
1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1142): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1192): Show |
1 | a0001c0002t0005g0075 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1203): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(1418): Show |
1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(1429): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(950): Show |
1 | a0001c0001t0008g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(961): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGAGACC others(2044): Show |
1 | a0001c0001t0033g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1265+3462_1265+346 others(2055): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492460
|
G | GGGGAGAC others(919): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1265+3476_1265+347 others(930): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492460 | |||||
| chr16:492477
|
C | CCCAGAGC others(916): Show |
1 | a0001c0002t0054g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(927): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(1168): Show |
1 | a0001c0001t0011g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(1179): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(2158): Show |
1 | a0001c0001t0007g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(2169): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(2622): Show |
1 | a0001c0001t0003g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(2633): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(2622): Show |
1 | a0001c0001t0003g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(2633): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(1289): Show |
1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(1300): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGAGC others(1294): Show |
1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1265+3481_1265+348 others(1305): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGGGC others(1446): Show |
1 | a0001c0001t0008g0063 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1457): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGGGC others(891): Show |
1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1265+3506_1265+350 others(902): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGGGC others(2561): Show |
1 | a0001c0001t0004g0056 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(2572): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGGGC others(1107): Show |
1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(1118): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | CCCAGGGC others(1100): Show |
1 | a0001c0002t0009g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(1111): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492477 | |||||
| chr16:492477
|
C | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1265+3477C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492477 | ||||||
| chr16:492482
|
G | A | 18 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0224others(15): Show | 18 | HG00558.hp1 HG00642.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1265+3482G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492482 | ||||||
| chr16:492482
|
G | GGCCCTTC others(149): Show |
1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(160): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492482 | |||||
| chr16:492486
|
C | CCCCGGGA others(829): Show |
1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+3486_1265+348 others(840): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492486 | ||||||
| chr16:492486
|
C | CT | 30 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(27): Show | 30 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1265+3487dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(552): Show |
1 | a0002c0003t0005g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(563): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(211): Show |
1 | a0002c0003t0005g0099 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(222): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(1698): Show |
1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1709): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(117): Show |
1 | a0001c0001t0010g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(128): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(305): Show |
1 | a0002c0003t0002g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(316): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(1325): Show |
1 | a0001c0001t0018g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1336): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTCCCCGG others(426): Show |
1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(437): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTTCCCGG others(1679): Show |
1 | a0002c0003t0018g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(1690): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTTCCCGG others(982): Show |
1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(993): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTTCCCGG others(679): Show |
1 | a0002c0003t0002g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(690): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTTCCCGG others(118): Show |
1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(129): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492486
|
C | CTTCCCGG others(87): Show |
1 | a0001c0001t0010g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(98): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492486 | |||||
| chr16:492487
|
T | C | 7 | a0001c0001t0003g0180a0001c0001t0003g0213a0001c0001t0007g0053others(4): Show | 7 | HG00323.hp2 HG00544.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265+3487T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TC | 74 | a0001c0001t0001g0119a0001c0001t0001g0161a0001c0001t0001g0182others(71): Show | 75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.1265+3490dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492487 | |||||
| chr16:492487
|
T | TCCCCGGG others(989): Show |
1 | a0002c0003t0002g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1000): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492487 | |||||
| chr16:492487
|
T | TCCCGGGA others(861): Show |
1 | a0001c0001t0001g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(872): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492487 | |||||
| chr16:492487
|
T | TCCCGGGA others(894): Show |
1 | a0001c0001t0001g0221 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(905): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492487 | |||||
| chr16:492487
|
T | TCCCGGGA others(363): Show |
1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1265+3520_1265+352 others(374): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492487 | |||||
| chr16:492487
|
T | TTC | 7 | a0001c0001t0001g0291a0001c0001t0002g0010a0001c0001t0006g0243others(4): Show | 7 | HG00735.hp2 HG01496.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265+3487_1265+348 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(395): Show |
1 | a0001c0001t0017g0087 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(406): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(333): Show |
1 | a0001c0001t0017g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(344): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(767): Show |
1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(778): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(1354): Show |
1 | a0001c0001t0015g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(1365): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(2075): Show |
1 | a0001c0001t0013g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(2086): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(2843): Show |
1 | a0001c0001t0013g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(2854): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(4379): Show |
1 | a0001c0001t0013g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(4390): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(4443): Show |
1 | a0001c0001t0013g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(4454): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(4507): Show |
1 | a0001c0001t0013g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(4518): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
T | TTCCCGGG others(303): Show |
1 | a0001c0001t0001g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1265+3487_1265+348 others(314): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492487
|
TCCCGGGA others(22): Show |
T | 1 | a0001c0001t0007g0137 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1265+3488_1265+351 others(33): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492487 | ||||||
| chr16:492488
|
C | T | 1 | a0001c0002t0044g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1265+3488C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492488 | ||||||
| chr16:492490
|
C | CCG | 11 | a0001c0001t0003g0133a0001c0001t0003g0135a0001c0001t0003g0209others(8): Show | 11 | HG00544.hp2 HG00609.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1265+3490_1265+349 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGAGA others(830): Show |
1 | a0001c0001t0020g0247 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(841): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGAGA others(830): Show |
1 | a0007c0015t0020g0199 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(841): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGAGA others(494): Show |
1 | a0001c0001t0001g0204 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(505): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGAGA others(306): Show |
1 | a0001c0001t0001g0240 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(317): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(923): Show |
1 | a0001c0001t0003g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(934): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1019): Show |
1 | a0001c0001t0011g0132 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1030): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1275): Show |
1 | a0001c0001t0034g0208 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1286): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1307): Show |
1 | a0001c0001t0003g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1318): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1371): Show |
1 | a0001c0001t0003g0235 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1382): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1723): Show |
4 | a0001c0001t0002g0002a0001c0001t0003g0210a0001c0001t0003g0211others(1): Show | 4 | NA18977.hp1 NA18981.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265+3490_1265+349 others(1734): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1787): Show |
1 | a0001c0001t0003g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1798): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1819): Show |
1 | a0001c0001t0047g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1830): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(2330): Show |
1 | a0001c0004t0008g0172 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(2341): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(2331): Show |
1 | a0001c0001t0007g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(2342): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(2523): Show |
1 | a0001c0001t0046g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(2534): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(2907): Show |
1 | a0001c0001t0045g0138 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(2918): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(1019): Show |
1 | a0001c0004t0003g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(1030): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CCGGGGAG others(731): Show |
1 | a0009c0009t0003g0130 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1265+3490_1265+349 others(742): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492490
|
C | CGGGAGAC others(56): Show |
1 | a0001c0001t0001g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(67): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492490 | |||||
| chr16:492490
|
C | G | 12 | a0001c0001t0001g0291a0001c0001t0002g0010a0001c0001t0006g0243others(9): Show | 12 | HG00735.hp2 HG01496.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1265+3490C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492490 | ||||||
| chr16:492494
|
A | G | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1265+3494A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492494 | ||||||
| chr16:492507
|
C | CCCAGAGC others(486): Show |
1 | a0001c0013t0052g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(497): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(1475): Show |
1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(1486): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(1155): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(1166): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(913): Show |
1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(924): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(2854): Show |
1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(2865): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(1702): Show |
1 | a0001c0001t0015g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(1713): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(712): Show |
2 | a0001c0002t0009g0040a0001c0002t0038g0038 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1265+3511_1265+351 others(723): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGAGC others(1278): Show |
1 | a0001c0002t0044g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1265+3511_1265+351 others(1289): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(1799): Show |
1 | a0001c0002t0009g0274 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1265+3520_1265+352 others(1810): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(1197): Show |
1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1265+3520_1265+352 others(1208): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(24): Show |
5 | a0001c0001t0001g0197a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG00642.hp1 HG01071.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265+3520_1265+352 others(35): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(475): Show |
1 | a0001c0002t0053g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1265+3520_1265+352 others(486): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(641): Show |
1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(652): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(641): Show |
1 | a0001c0001t0001g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(652): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(862): Show |
1 | a0001c0002t0009g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(873): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(1315): Show |
1 | a0001c0002t0009g0275 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(1326): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(1319): Show |
1 | a0001c0002t0026g0170 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(1330): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | CCCAGGGC others(2203): Show |
1 | a0001c0002t0009g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(2214): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492507 | |||||
| chr16:492507
|
C | T | 145 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(142): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1265+3507C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492507 | ||||||
| chr16:492512
|
G | A | 9 | a0001c0001t0001g0266a0001c0001t0005g0066a0001c0001t0008g0294others(6): Show | 9 | HG00558.hp1 HG00738.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1265+3512G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492512 | ||||||
| chr16:492516
|
C | CT | 89 | a0001c0001t0001g0119a0001c0001t0001g0205a0001c0001t0001g0206others(86): Show | 89 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1265+3517dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492516 | |||||
| chr16:492516
|
C | CTCCCCGG others(180): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1265+3520_1265+352 others(191): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492516 | |||||
| chr16:492516
|
C | CTTCCCGG others(1922): Show |
1 | a0001c0001t0060g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1265+3517_1265+351 others(1933): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492516 | |||||
| chr16:492516
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1265+3516C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492516 | ||||||
| chr16:492517
|
T | C | 2 | a0001c0001t0021g0001a0001c0001t0025g0021 | 3 | HG01069.hp1 HG01071.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1265+3517T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492517 | ||||||
| chr16:492517
|
T | TC | 18 | a0001c0001t0001g0283a0001c0001t0002g0015a0001c0001t0002g0264others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.1265+3520dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492517 | |||||
| chr16:492520
|
C | CGGGAGAC others(117): Show |
1 | a0001c0001t0010g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1265+3542_1265+354 others(128): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 492520 | |||||
| chr16:492520
|
C | G | 1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1265+3520C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492520 | ||||||
| chr16:492524
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0008g0265 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1265+3524A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492524 | ||||||
| chr16:492530
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+3530G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492530 | ||||||
| chr16:492536
|
G | A | 1 | a0001c0001t0012g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1265+3536G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492536 | ||||||
| chr16:492537
|
T | C | 4 | a0001c0001t0006g0227a0001c0001t0006g0243a0001c0001t0025g0021others(1): Show | 4 | HG01496.hp1 HG02735.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265+3537T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492537 | ||||||
| chr16:492610
|
C | T | 1 | a0001c0001t0012g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1265+3610C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492610 | ||||||
| chr16:492622
|
C | G | 1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1265+3622C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492622 | ||||||
| chr16:492642
|
T | C | 1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1265+3642T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492642 | ||||||
| chr16:492645
|
G | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1265+3645G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492645 | ||||||
| chr16:492724
|
G | C | 48 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0078others(45): Show | 49 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1265+3724G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492724 | ||||||
| chr16:492727
|
A | G | 162 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0119others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1265+3727A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492727 | ||||||
| chr16:492733
|
G | A | 16 | a0001c0001t0001g0159a0001c0001t0001g0197a0001c0001t0001g0198others(13): Show | 16 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1265+3733G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492733 | ||||||
| chr16:492738
|
T | C | 1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1265+3738T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492738 | ||||||
| chr16:492768
|
C | G | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265+3768C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492768 | ||||||
| chr16:492768
|
C | T | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0220others(3): Show | 6 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265+3768C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492768 | ||||||
| chr16:492772
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0015g0122 | 3 | HG01981.hp2 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1265+3772C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492772 | ||||||
| chr16:492845
|
G | A | 19 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(16): Show | 19 | HG01243.hp1 HG01261.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1265+3845G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492845 | ||||||
| chr16:492862
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1265+3862T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492862 | ||||||
| chr16:492863
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1265+3863G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492863 | ||||||
| chr16:492924
|
G | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266-3900G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492924 | ||||||
| chr16:492965
|
G | A | 1 | a0001c0001t0049g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1266-3859G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 492965 | ||||||
| chr16:493011
|
G | A | 16 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(13): Show | 16 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1266-3813G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493011 | ||||||
| chr16:493072
|
G | A | 2 | a0001c0006t0058g0111a0004c0007t0022g0067 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1266-3752G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493072 | ||||||
| chr16:493079
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1266-3745T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493079 | ||||||
| chr16:493251
|
C | CA | 7 | a0001c0001t0001g0182a0001c0001t0001g0218a0001c0001t0003g0180others(4): Show | 7 | HG01952.hp2 HG02080.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1266-3553dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493251 | |||||
| chr16:493251
|
CA | C | 21 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0214others(18): Show | 21 | HG00280.hp1 HG01070.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1266-3553delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493251 | |||||
| chr16:493251
|
CAA | C | 90 | a0001c0001t0001g0119a0001c0001t0001g0283a0001c0001t0002g0002others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1266-3554_1266-355 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493251 | |||||
| chr16:493251
|
CAAAAAAA | C | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-3559_1266-355 others(11): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493251 | |||||
| chr16:493312
|
A | G | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266-3512A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493312 | ||||||
| chr16:493357
|
T | C | 116 | a0001c0001t0001g0119a0001c0001t0001g0283a0001c0001t0002g0002others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1266-3467T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493357 | ||||||
| chr16:493399
|
T | G | 1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1266-3425T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493399 | ||||||
| chr16:493490
|
G | A | 2 | a0001c0001t0001g0205a0001c0019t0002g0012 | 2 | HG01192.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1266-3334G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493490 | ||||||
| chr16:493641
|
T | C | 2 | a0001c0001t0010g0217a0001c0001t0010g0222 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1266-3183T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493641 | ||||||
| chr16:493662
|
A | AGTGGTGC others(290): Show |
2 | a0001c0001t0001g0248a0001c0001t0020g0236 | 2 | HG00438.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1266-3028_1266-273 others(301): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493662 | |||||
| chr16:493667
|
T | C | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-3157T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493667 | ||||||
| chr16:493675
|
C | T | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1266-3149C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493675 | ||||||
| chr16:493687
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1266-3137A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493687 | ||||||
| chr16:493752
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1266-3072G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493752 | ||||||
| chr16:493793
|
C | G | 2 | a0001c0001t0001g0006a0002c0003t0011g0102 | 2 | HG01106.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1266-3031C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493793 | ||||||
| chr16:493796
|
G | A | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266-3028G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493796 | ||||||
| chr16:493796
|
GGGGTTTC others(290): Show |
G | 15 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0160others(12): Show | 15 | HG01074.hp2 HG02132.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.1266-2981_1266-268 others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 493796 | |||||
| chr16:493808
|
T | C | 1 | a0001c0001t0042g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1266-3016T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493808 | ||||||
| chr16:493834
|
C | T | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1266-2990C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493834 | ||||||
| chr16:493843
|
T | C | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1266-2981T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493843 | ||||||
| chr16:493845
|
A | G | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1266-2979A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493845 | ||||||
| chr16:493848
|
C | T | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1266-2976C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493848 | ||||||
| chr16:493871
|
C | G | 1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266-2953C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493871 | ||||||
| chr16:493880
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266-2944T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493880 | ||||||
| chr16:493902
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1266-2922A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493902 | ||||||
| chr16:493957
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1266-2867G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493957 | ||||||
| chr16:493996
|
C | A | 7 | a0001c0001t0021g0001a0001c0001t0025g0021a0001c0001t0025g0109others(4): Show | 8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266-2828C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 493996 | ||||||
| chr16:494025
|
T | TCCCGAGT others(291): Show |
1 | a0002c0003t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1266-2732_1266-273 others(302): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494025 | |||||
| chr16:494027
|
C | T | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2797C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494027 | ||||||
| chr16:494053
|
A | G | 153 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(150): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1266-2771A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494053 | ||||||
| chr16:494054
|
T | C | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2770T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494054 | ||||||
| chr16:494057
|
C | T | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2767C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494057 | ||||||
| chr16:494058
|
C | A | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2766C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494058 | ||||||
| chr16:494061
|
A | G | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2763A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494061 | ||||||
| chr16:494064
|
T | C | 156 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1266-2760T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494064 | ||||||
| chr16:494070
|
A | AT | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2754_1266-275 others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494070 | ||||||
| chr16:494071
|
C | T | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2753C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494071 | ||||||
| chr16:494084
|
A | G | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2740A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494084 | ||||||
| chr16:494090
|
C | G | 157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2734C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494090 | ||||||
| chr16:494093
|
A | G | 117 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(114): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1266-2731A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494093 | ||||||
| chr16:494105
|
T | TGTTAGCC others(6): Show |
157 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0010others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1266-2717_1266-271 others(17): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494105 | |||||
| chr16:494118
|
G | GGACCTCG others(601): Show |
1 | a0001c0001t0005g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1266-2685_1266-268 others(612): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494118 | |||||
| chr16:494118
|
G | GGACCTCG others(304): Show |
1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1266-2685_1266-268 others(315): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494118 | |||||
| chr16:494118
|
G | GGACCTCG others(304): Show |
9 | a0001c0001t0001g0119a0001c0001t0002g0002a0001c0001t0002g0015others(6): Show | 9 | HG01258.hp2 HG01261.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266-2685_1266-268 others(315): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494118 | |||||
| chr16:494118
|
G | T | 158 | a0001c0001t0001g0283a0001c0001t0002g0005a0001c0001t0002g0009others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1266-2706G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494118 | ||||||
| chr16:494250
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1266-2574G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494250 | ||||||
| chr16:494479
|
G | A | 71 | a0001c0001t0001g0119a0001c0001t0001g0283a0001c0001t0002g0005others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.1266-2345G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494479 | ||||||
| chr16:494664
|
G | A | 194 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0283others(191): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1266-2160G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494664 | ||||||
| chr16:494745
|
G | A | 2 | a0001c0001t0018g0043a0001c0014t0039g0112 | 2 | HG02280.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1266-2079G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494745 | ||||||
| chr16:494745
|
G | C | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1266-2079G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494745 | ||||||
| chr16:494762
|
T | TGAGGTGG others(2166): Show |
1 | a0001c0001t0008g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(2177): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(977): Show |
23 | a0001c0001t0002g0078a0001c0001t0003g0060a0001c0001t0003g0076others(20): Show | 23 | HG00544.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1266-1998_1266-199 others(988): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(977): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(988): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(2822): Show |
2 | a0001c0001t0025g0021a0001c0001t0025g0109 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1266-1998_1266-199 others(2833): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(936): Show |
2 | a0001c0001t0003g0180a0001c0001t0004g0201 | 2 | NA18939.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1266-1998_1266-199 others(947): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(977): Show |
9 | a0001c0001t0004g0051a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 9 | HG00609.hp2 HG00673.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266-1998_1266-199 others(988): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(2904): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(2915): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(4257): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(4268): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(2658): Show |
2 | a0001c0002t0019g0285a0001c0002t0043g0025 | 2 | HG01106.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1266-1998_1266-199 others(2669): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(731): Show |
1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(742): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494762
|
T | TGAGGTGG others(1305): Show |
2 | a0001c0002t0009g0274a0001c0002t0009g0284 | 2 | NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1266-2031_1266-203 others(1316): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494762 | |||||
| chr16:494794
|
C | T | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-2030C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494794 | ||||||
| chr16:494799
|
C | CTGCAGAG others(34): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(45): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494799 | |||||
| chr16:494799
|
C | T | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1266-2025C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494799 | ||||||
| chr16:494803
|
A | AGAGGTGG others(444): Show |
1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(455): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494803 | |||||
| chr16:494803
|
A | AGAGGTGG others(75): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(86): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494803 | |||||
| chr16:494803
|
A | AGAGGTGG others(813): Show |
1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1266-1998_1266-199 others(824): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494803 | |||||
| chr16:494811
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1266-2013G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494811 | ||||||
| chr16:494824
|
G | T | 3 | a0001c0001t0001g0242a0001c0002t0009g0274a0001c0002t0009g0284 | 3 | HG01175.hp2 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1266-2000G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494824 | ||||||
| chr16:494827
|
T | A | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-1997T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494827 | ||||||
| chr16:494827
|
T | G | 111 | a0001c0001t0002g0002a0001c0001t0002g0078a0001c0001t0003g0060others(108): Show | 112 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1266-1997T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494827 | ||||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0012g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0004t0008g0172 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1633): Show |
1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1644): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2453): Show |
5 | a0001c0001t0001g0193a0001c0001t0001g0218a0001c0001t0001g0232others(2): Show | 5 | HG00099.hp2 HG01069.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2464): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2781): Show |
1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2792): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2781): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0203others(3): Show | 6 | HG01106.hp2 HG01516.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2792): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1633): Show |
2 | a0003c0005t0014g0022a0003c0005t0014g0024 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(1644): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2698): Show |
1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2709): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(1): Show | 4 | HG00438.hp2 HG00597.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1182): Show |
1 | a0001c0001t0002g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1193): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1182): Show |
2 | a0001c0001t0005g0105a0002c0003t0002g0293 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(1193): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1633): Show |
47 | a0001c0001t0001g0182a0001c0001t0001g0266a0001c0001t0001g0268others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(1644): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
5 | a0001c0001t0001g0159a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02165.hp2 NA18957.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0144 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0020g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0006g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
51 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0161others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0061g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0010g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1223): Show |
9 | a0001c0001t0010g0004a0001c0001t0016g0003a0001c0001t0017g0049others(6): Show | 9 | HG00423.hp2 HG01258.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(1234): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0165 | 2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2002): Show |
1 | a0001c0001t0002g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2013): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2002): Show |
1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2013): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2699): Show |
1 | a0001c0001t0001g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2710): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1100): Show |
1 | a0001c0002t0002g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1111): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2822): Show |
1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2833): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1756): Show |
2 | a0001c0001t0002g0017a0001c0011t0002g0019 | 2 | NA18950.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1266-1973_1266-197 others(1767): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1223): Show |
1 | a0001c0002t0005g0079 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1234): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(2863): Show |
1 | a0001c0004t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(2874): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1633): Show |
1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1644): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1223): Show |
1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1234): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494827
|
T | TGGGAGGT others(1592): Show |
1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1266-1973_1266-197 others(1603): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 494827 | |||||
| chr16:494840
|
C | T | 67 | a0001c0001t0002g0002a0001c0001t0003g0125a0001c0001t0003g0133others(64): Show | 67 | HG00544.hp2 HG00609.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.1266-1984C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494840 | ||||||
| chr16:494844
|
A | T | 7 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258others(4): Show | 7 | HG02717.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1266-1980A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494844 | ||||||
| chr16:494852
|
G | C | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1266-1972G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494852 | ||||||
| chr16:494865
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1266-1959G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494865 | ||||||
| chr16:494868
|
G | A | 151 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0115others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1266-1956G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494868 | ||||||
| chr16:494868
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1266-1956G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494868 | ||||||
| chr16:494885
|
A | T | 71 | a0001c0001t0002g0002a0001c0001t0003g0125a0001c0001t0003g0133others(68): Show | 72 | HG00544.hp2 HG00609.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.1266-1939A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494885 | ||||||
| chr16:494909
|
G | A | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-1915G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494909 | ||||||
| chr16:494909
|
G | T | 3 | a0001c0001t0002g0086a0001c0001t0005g0105a0002c0003t0002g0293 | 3 | HG02818.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1266-1915G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494909 | ||||||
| chr16:494917
|
C | G | 3 | a0001c0001t0001g0182a0001c0001t0010g0188a0001c0001t0031g0166 | 3 | HG02886.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1266-1907C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494917 | ||||||
| chr16:494926
|
T | A | 289 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1266-1898T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494926 | ||||||
| chr16:494935
|
A | G | 2 | a0001c0002t0009g0274a0001c0002t0009g0284 | 2 | NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1266-1889A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494935 | ||||||
| chr16:494948
|
C | G | 1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266-1876C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494948 | ||||||
| chr16:494950
|
G | T | 206 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1266-1874G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494950 | ||||||
| chr16:494967
|
T | A | 87 | a0001c0001t0001g0290a0001c0001t0001g0292a0001c0001t0002g0002others(84): Show | 88 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1266-1857T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494967 | ||||||
| chr16:494984
|
A | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266-1840A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494984 | ||||||
| chr16:494991
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1266-1833G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 494991 | ||||||
| chr16:495008
|
A | T | 208 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1266-1816A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495008 | ||||||
| chr16:495014
|
G | C | 205 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1266-1810G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495014 | ||||||
| chr16:495014
|
G | GGCAGGAT others(1633): Show |
2 | a0001c0001t0001g0290a0001c0001t0001g0292 | 2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1266-1809_1266-180 others(1644): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2289): Show |
3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(2300): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2248): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2259): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
1 | a0001c0001t0033g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
1 | a0001c0001t0060g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2289): Show |
3 | a0004c0007t0022g0067a0004c0007t0022g0186a0005c0017t0037g0100 | 3 | HG02717.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(2300): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2289): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2300): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(1715): Show |
1 | a0001c0001t0003g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(1726): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
29 | a0001c0001t0002g0002a0001c0001t0003g0125a0001c0001t0003g0133others(26): Show | 29 | HG00544.hp2 HG00609.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
3 | a0001c0001t0015g0136a0001c0001t0041g0126a0001c0001t0056g0124 | 3 | HG02572.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(690): Show |
4 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(701): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(690): Show |
2 | a0001c0001t0013g0029a0001c0001t0013g0033 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(701): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(1674): Show |
2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(1685): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(9218): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(9229): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2494): Show |
1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2505): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(895): Show |
1 | a0001c0001t0035g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(906): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(2207): Show |
1 | a0001c0001t0003g0261 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(2218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(1305): Show |
4 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0023g0103others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(1316): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(1756): Show |
7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1266-1780_1266-177 others(1767): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(895): Show |
1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1266-1793_1266-179 others(906): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495014
|
G | GGGAGGAT others(894): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1266-1793_1266-179 others(905): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495014 | |||||
| chr16:495015
|
G | A | 1 | a0001c0002t0002g0255 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1266-1809G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495015 | ||||||
| chr16:495018
|
G | GGATCACA others(1428): Show |
3 | a0001c0002t0019g0106a0001c0002t0053g0271a0001c0002t0054g0267 | 3 | HG02109.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(1439): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1345): Show |
1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(1356): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1428): Show |
1 | a0001c0001t0015g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(1439): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1428): Show |
8 | a0001c0002t0009g0040a0001c0002t0009g0081a0001c0002t0009g0253others(5): Show | 8 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(1439): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1428): Show |
1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(1439): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1223): Show |
1 | a0001c0002t0044g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1266-1774_1266-177 others(1234): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(116): Show |
2 | a0001c0002t0009g0274a0001c0002t0009g0284 | 2 | NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1266-1774_1266-177 others(127): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495018
|
G | GGATCACA others(1305): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1266-1796_1266-179 others(1316): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 495018 | |||||
| chr16:495209
|
A | T | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1266-1615A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495209 | ||||||
| chr16:495267
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1266-1557C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495267 | ||||||
| chr16:495274
|
G | A | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1266-1550G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495274 | ||||||
| chr16:495293
|
A | G | 2 | a0001c0001t0005g0105a0002c0003t0002g0293 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266-1531A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495293 | ||||||
| chr16:495313
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1266-1511C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495313 | ||||||
| chr16:495339
|
C | G | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266-1485C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495339 | ||||||
| chr16:495379
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0242 | 3 | HG01175.hp2 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1266-1445A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495379 | ||||||
| chr16:495389
|
T | C | 2 | a0001c0002t0009g0040a0001c0002t0038g0038 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1266-1435T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495389 | ||||||
| chr16:495454
|
C | G | 3 | a0001c0004t0003g0116a0001c0004t0008g0172a0009c0009t0003g0130 | 3 | HG02129.hp1 NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1266-1370C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495454 | ||||||
| chr16:495465
|
G | A | 18 | a0001c0001t0002g0005a0001c0001t0015g0039a0001c0002t0009g0040others(15): Show | 18 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266-1359G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495465 | ||||||
| chr16:495523
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1266-1301G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495523 | ||||||
| chr16:495713
|
G | A | 2 | a0001c0002t0002g0149a0001c0002t0002g0167 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1266-1111G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495713 | ||||||
| chr16:495786
|
T | C | 17 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(14): Show | 17 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1266-1038T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495786 | ||||||
| chr16:495900
|
G | A | 1 | a0001c0001t0012g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1266-924G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495900 | ||||||
| chr16:495923
|
A | T | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266-901A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495923 | ||||||
| chr16:495944
|
T | G | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266-880T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495944 | ||||||
| chr16:495952
|
G | A | 1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1266-872G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495952 | ||||||
| chr16:495996
|
C | T | 52 | a0001c0001t0002g0078a0001c0001t0003g0060a0001c0001t0003g0076others(49): Show | 52 | HG00544.hp1 HG00609.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1266-828C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 495996 | ||||||
| chr16:496045
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0232a0001c0001t0001g0281 | 3 | HG01928.hp1 HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1266-779C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496045 | ||||||
| chr16:496148
|
C | T | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1266-676C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496148 | ||||||
| chr16:496269
|
C | G | 1 | a0001c0001t0010g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1266-555C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496269 | ||||||
| chr16:496279
|
A | C | 1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1266-545A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496279 | ||||||
| chr16:496280
|
C | A | 1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1266-544C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496280 | ||||||
| chr16:496321
|
T | C | 21 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(18): Show | 21 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1266-503T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496321 | ||||||
| chr16:496418
|
G | A | 4 | a0001c0001t0008g0294a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG02717.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266-406G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496418 | ||||||
| chr16:496426
|
C | G | 53 | a0001c0001t0001g0006a0001c0001t0002g0002a0001c0001t0002g0078others(50): Show | 53 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1266-398C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496426 | ||||||
| chr16:496430
|
T | G | 1 | a0001c0001t0021g0001 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1266-394T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496430 | ||||||
| chr16:496439
|
G | A | 5 | a0002c0003t0002g0093a0002c0003t0002g0094a0002c0003t0002g0097others(2): Show | 5 | NA18947.hp1 NA18977.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266-385G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496439 | ||||||
| chr16:496688
|
C | T | 16 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(13): Show | 16 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1266-136C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496688 | ||||||
| chr16:496693
|
G | T | 8 | a0001c0001t0001g0268a0001c0001t0001g0286a0001c0001t0001g0287others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1266-131G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496693 | ||||||
| chr16:496726
|
C | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1266-98C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 5/13 | chr16 | 496726 | ||||||
| chr16:496884
|
G | A | 1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1301+25G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 496884 | ||||||
| chr16:496934
|
T | TAA | 3 | a0001c0001t0015g0122a0001c0001t0033g0128a0001c0001t0060g0108 | 3 | HG02895.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1301+78_1301+79dup others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 496934 | |||||
| chr16:497010
|
A | G | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+151A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497010 | ||||||
| chr16:497108
|
G | A | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1301+249G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497108 | ||||||
| chr16:497185
|
G | A | 1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1301+326G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497185 | ||||||
| chr16:497207
|
C | T | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1301+348C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497207 | ||||||
| chr16:497209
|
G | T | 2 | a0001c0001t0005g0105a0002c0003t0002g0293 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1301+350G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497209 | ||||||
| chr16:497297
|
T | C | 60 | a0001c0001t0002g0002a0001c0001t0003g0060a0001c0001t0003g0125others(57): Show | 60 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1301+438T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497297 | ||||||
| chr16:497458
|
T | C | 21 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(18): Show | 21 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+599T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497458 | ||||||
| chr16:497530
|
C | T | 57 | a0001c0001t0002g0002a0001c0001t0003g0060a0001c0001t0003g0125others(54): Show | 57 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1301+671C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497530 | ||||||
| chr16:497541
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1301+682C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497541 | ||||||
| chr16:497572
|
T | C | 3 | a0001c0002t0019g0037a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1301+713T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497572 | ||||||
| chr16:497939
|
C | CA | 6 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0004g0074others(3): Show | 6 | HG00738.hp2 HG01243.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1301+1096dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 497939 | |||||
| chr16:497939
|
C | CAA | 16 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(13): Show | 16 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1301+1095_1301+109 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 497939 | |||||
| chr16:497956
|
T | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1301+1097T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 497956 | ||||||
| chr16:497971
|
TA | T | 7 | a0001c0001t0001g0229a0001c0001t0003g0180a0001c0001t0008g0148others(4): Show | 7 | HG01070.hp2 HG01261.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1301+1124delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 497971 | |||||
| chr16:498364
|
G | A | 8 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0011g0110others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301+1505G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498364 | ||||||
| chr16:498377
|
G | A | 1 | a0001c0002t0002g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1301+1518G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498377 | ||||||
| chr16:498441
|
C | T | 1 | a0001c0001t0011g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1301+1582C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498441 | ||||||
| chr16:498573
|
C | G | 22 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(19): Show | 22 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1301+1714C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498573 | ||||||
| chr16:498633
|
C | T | 17 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(14): Show | 17 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1301+1774C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498633 | ||||||
| chr16:498643
|
C | G | 1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1301+1784C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498643 | ||||||
| chr16:498663
|
C | T | 5 | a0001c0001t0015g0122a0001c0001t0015g0136a0001c0001t0041g0126others(2): Show | 5 | HG02572.hp1 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1301+1804C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498663 | ||||||
| chr16:498794
|
C | T | 2 | a0001c0006t0058g0111a0001c0012t0059g0107 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1301+1935C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498794 | ||||||
| chr16:498826
|
T | TTAGGGGC | 3 | a0001c0002t0019g0037a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1301+1985_1301+199 others(11): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 498826 | |||||
| chr16:498826
|
T | TTAGGGGC others(7): Show |
16 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(13): Show | 16 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1301+1978_1301+199 others(18): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 498826 | |||||
| chr16:498829
|
G | GGGGCTAG others(6): Show |
1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1301+1974_1301+198 others(17): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 498829 | |||||
| chr16:498895
|
T | G | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1301+2036T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498895 | ||||||
| chr16:498908
|
C | G | 7 | a0001c0001t0021g0001a0001c0001t0025g0021a0001c0001t0025g0109others(4): Show | 8 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1301+2049C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498908 | ||||||
| chr16:498937
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1301+2078G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 498937 | ||||||
| chr16:498938
|
T | TA | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1301+2080dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 498938 | |||||
| chr16:499144
|
G | A | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1301+2285G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499144 | ||||||
| chr16:499161
|
G | A | 22 | a0001c0001t0008g0294a0001c0001t0013g0026a0001c0001t0013g0027others(19): Show | 22 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1301+2302G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499161 | ||||||
| chr16:499254
|
G | A | 1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1301+2395G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499254 | ||||||
| chr16:499310
|
G | A | 294 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1301+2451G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499310 | ||||||
| chr16:499404
|
C | T | 2 | a0001c0006t0058g0111a0001c0012t0059g0107 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1301+2545C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499404 | ||||||
| chr16:499405
|
T | C | 2 | a0001c0006t0058g0111a0001c0012t0059g0107 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1301+2546T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499405 | ||||||
| chr16:499415
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1301+2556C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499415 | ||||||
| chr16:499429
|
G | C | 1 | a0001c0001t0006g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1301+2570G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499429 | ||||||
| chr16:499520
|
G | A | 1 | a0001c0002t0009g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1301+2661G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499520 | ||||||
| chr16:499578
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0203a0001c0001t0001g0215 | 3 | HG01106.hp2 HG01516.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1301+2719A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499578 | ||||||
| chr16:499605
|
G | C | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1301+2746G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499605 | ||||||
| chr16:499754
|
C | T | 59 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1301+2895C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499754 | ||||||
| chr16:499795
|
C | CA | 32 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0214others(29): Show | 32 | HG00408.hp2 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1301+2958dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 499795 | |||||
| chr16:499795
|
CA | C | 78 | a0001c0001t0001g0160a0001c0001t0001g0232a0001c0001t0001g0234others(75): Show | 78 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1301+2958delA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 499795 | |||||
| chr16:499907
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1301+3048G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 499907 | ||||||
| chr16:500126
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1302-2878C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500126 | ||||||
| chr16:500169
|
G | A | 2 | a0001c0001t0001g0115a0001c0014t0039g0112 | 2 | HG03654.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1302-2835G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500169 | ||||||
| chr16:500337
|
T | C | 19 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(16): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302-2667T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500337 | ||||||
| chr16:500405
|
G | A | 7 | a0001c0001t0004g0074a0001c0001t0008g0063a0001c0001t0008g0065others(4): Show | 7 | HG02074.hp2 NA18967.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302-2599G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500405 | ||||||
| chr16:500613
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1302-2391G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500613 | ||||||
| chr16:500687
|
C | CA | 148 | a0001c0001t0001g0072a0001c0001t0001g0115a0001c0001t0001g0117others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1302-2288dupA | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 500687 | |||||
| chr16:500687
|
C | CAA | 65 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0120others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1302-2289_1302-228 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 500687 | |||||
| chr16:500687
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1302-2299_1302-228 others(16): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 500687 | |||||
| chr16:500721
|
A | T | 1 | a0001c0001t0001g0221 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1302-2283A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500721 | ||||||
| chr16:500756
|
T | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1302-2248T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500756 | ||||||
| chr16:500887
|
G | A | 2 | a0001c0001t0006g0196a0001c0001t0006g0238 | 2 | HG02027.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1302-2117G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500887 | ||||||
| chr16:500975
|
G | A | 3 | a0001c0001t0002g0078a0001c0001t0014g0142a0001c0001t0014g0143 | 3 | HG00642.hp2 HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1302-2029G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 500975 | ||||||
| chr16:501226
|
C | T | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-1778C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501226 | ||||||
| chr16:501251
|
C | T | 1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1302-1753C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501251 | ||||||
| chr16:501302
|
G | C | 8 | a0001c0001t0001g0268a0001c0001t0001g0286a0001c0001t0001g0287others(5): Show | 8 | HG02895.hp1 HG02897.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302-1702G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501302 | ||||||
| chr16:501342
|
ACTCGGAG others(172): Show |
A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1302-1644_1302-146 others(4): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 501342 | |||||
| chr16:501361
|
A | C | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-1643A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501361 | ||||||
| chr16:501684
|
T | C | 1 | a0001c0001t0014g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1302-1320T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501684 | ||||||
| chr16:501767
|
G | A | 1 | a0001c0001t0012g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1302-1237G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501767 | ||||||
| chr16:501844
|
G | A | 1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1302-1160G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501844 | ||||||
| chr16:501892
|
T | C | 19 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(16): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302-1112T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 501892 | ||||||
| chr16:502060
|
C | T | 3 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0014g0177 | 3 | HG01981.hp2 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1302-944C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502060 | ||||||
| chr16:502123
|
C | T | 6 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(3): Show | 6 | HG01243.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302-881C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502123 | ||||||
| chr16:502128
|
C | T | 1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1302-876C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502128 | ||||||
| chr16:502147
|
G | C | 6 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(3): Show | 6 | HG01243.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302-857G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502147 | ||||||
| chr16:502150
|
C | T | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-854C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502150 | ||||||
| chr16:502164
|
G | C | 1 | a0001c0001t0049g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1302-840G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502164 | ||||||
| chr16:502197
|
C | T | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302-807C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502197 | ||||||
| chr16:502207
|
A | G | 19 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(16): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302-797A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502207 | ||||||
| chr16:502231
|
C | A | 3 | a0001c0001t0015g0123a0001c0001t0015g0184a0001c0001t0024g0185 | 3 | HG01891.hp2 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1302-773C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502231 | ||||||
| chr16:502344
|
C | T | 26 | a0001c0001t0003g0125a0001c0001t0003g0133a0001c0001t0003g0135others(23): Show | 26 | HG00544.hp2 HG00609.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1302-660C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502344 | ||||||
| chr16:502423
|
G | A | 1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1302-581G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502423 | ||||||
| chr16:502448
|
G | A | 32 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(29): Show | 32 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1302-556G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502448 | ||||||
| chr16:502452
|
G | A | 1 | a0001c0001t0004g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1302-552G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502452 | ||||||
| chr16:502525
|
C | G | 1 | a0001c0001t0012g0189 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1302-479C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502525 | ||||||
| chr16:502621
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1302-383C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502621 | ||||||
| chr16:502621
|
C | T | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-383C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502621 | ||||||
| chr16:502712
|
G | A | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1302-292G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502712 | ||||||
| chr16:502731
|
A | G | 19 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(16): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1302-273A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502731 | ||||||
| chr16:502819
|
A | C | 1 | a0001c0001t0007g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1302-185A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502819 | ||||||
| chr16:502835
|
C | T | 3 | a0001c0001t0011g0256a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG02717.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1302-169C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502835 | ||||||
| chr16:502946
|
C | T | 1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1302-58C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | chr16 | 502946 | ||||||
| chr16:502981
|
CTGT | C | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1302-16_1302-14del others(3): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 502981 | |||||
| chr16:503116
|
G | A | 32 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(29): Show | 32 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1395+19G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503116 | ||||||
| chr16:503401
|
G | A | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395+304G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503401 | ||||||
| chr16:503442
|
G | A | 1 | a0001c0001t0005g0013 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1395+345G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503442 | ||||||
| chr16:503564
|
A | G | 4 | a0001c0001t0006g0196a0001c0001t0006g0207a0001c0001t0006g0238others(1): Show | 4 | HG01346.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+467A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503564 | ||||||
| chr16:503608
|
G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1395+511G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503608 | ||||||
| chr16:503945
|
G | A | 19 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(16): Show | 19 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1395+848G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503945 | ||||||
| chr16:503957
|
TCCTCCTG others(13): Show |
T | 228 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(225): Show | 229 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1395+899_1395+918d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 503957 | |||||
| chr16:503975
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1395+878C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503975 | ||||||
| chr16:503976
|
CACCTCCT others(33): Show |
C | 1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1395+899_1395+938d others(42): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 503976 | |||||
| chr16:503977
|
A | T | 1 | a0001c0002t0002g0255 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1395+880A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503977 | ||||||
| chr16:503996
|
C | T | 18 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(15): Show | 18 | HG01106.hp1 HG01361.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1395+899C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 503996 | ||||||
| chr16:503996
|
CACCTCCT others(13): Show |
C | 43 | a0001c0001t0001g0283a0001c0001t0002g0002a0001c0001t0002g0005others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1395+939_1395+958d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 503996 | |||||
| chr16:504007
|
CCCCCTCA others(12): Show |
C | 1 | a0001c0001t0007g0137 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1395+915_1395+933d others(21): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504007 | |||||
| chr16:504016
|
T | C | 2 | a0001c0002t0002g0255a0001c0014t0039g0112 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1395+919T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504016 | ||||||
| chr16:504017
|
A | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+920A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504017 | ||||||
| chr16:504032
|
T | TCACCTCC others(70): Show |
2 | a0001c0002t0019g0106a0001c0002t0043g0025 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1395+938_1395+939i others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504032 | |||||
| chr16:504032
|
T | TCACCTCC others(167): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1395+938_1395+939i others(176): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504032 | |||||
| chr16:504035
|
C | CCTCCTCC others(166): Show |
2 | a0001c0002t0002g0158a0001c0002t0002g0171 | 2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1395+938_1395+939i others(175): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504035 | ||||||
| chr16:504036
|
T | C | 20 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1395+939T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504036 | ||||||
| chr16:504037
|
A | T | 20 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1395+940A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504037 | ||||||
| chr16:504041
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+944C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504041 | ||||||
| chr16:504042
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+945C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504042 | ||||||
| chr16:504055
|
C | CCTCCTGT others(68): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+963_1395+964i others(77): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504055 | |||||
| chr16:504055
|
C | CCTCCTTG others(68): Show |
1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1395+963_1395+964i others(77): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504055 | |||||
| chr16:504055
|
C | CCTCCTTG others(88): Show |
8 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(5): Show | 8 | HG01167.hp2 HG01361.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+963_1395+964i others(97): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504055 | |||||
| chr16:504057
|
T | TCCTTGTG others(10): Show |
5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+963_1395+964i others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504057 | |||||
| chr16:504075
|
C | G | 1 | a0001c0002t0009g0041 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1395+978C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504075 | ||||||
| chr16:504085
|
T | C | 15 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(12): Show | 15 | HG01167.hp2 HG01361.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1395+988T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504085 | ||||||
| chr16:504123
|
A | ACCCCCTT others(86): Show |
1 | a0001c0001t0008g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1395+1031_1395+103 others(97): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504123 | |||||
| chr16:504129
|
C | CTTGCCTC others(88): Show |
1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1395+1032_1395+103 others(99): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504129 | ||||||
| chr16:504129
|
C | CTTGCCTC others(87): Show |
3 | a0001c0001t0008g0063a0001c0001t0011g0179a0001c0001t0051g0064 | 3 | NA19004.hp2 NA19012.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1395+1032_1395+103 others(98): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504129 | ||||||
| chr16:504129
|
C | T | 10 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(7): Show | 10 | HG01167.hp2 HG01361.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+1032C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504129 | ||||||
| chr16:504145
|
C | G | 2 | a0002c0003t0007g0095a0002c0003t0007g0096 | 2 | NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1395+1048C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504145 | ||||||
| chr16:504146
|
C | CG | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+1049_1395+105 others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504146 | ||||||
| chr16:504159
|
T | C | 16 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0251others(13): Show | 16 | HG01167.hp2 HG01361.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395+1062T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504159 | ||||||
| chr16:504172
|
T | TCCTCCTG others(167): Show |
2 | a0001c0002t0002g0158a0001c0002t0002g0171 | 2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1395+1098_1395+109 others(178): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504172 | |||||
| chr16:504190
|
C | G | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395+1093C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504190 | ||||||
| chr16:504200
|
C | T | 2 | a0001c0002t0009g0041a0001c0014t0039g0112 | 2 | HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1395+1103C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504200 | ||||||
| chr16:504201
|
AC | A | 10 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(7): Show | 10 | HG02630.hp1 HG03516.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+1109delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504201 | |||||
| chr16:504238
|
A | AC | 11 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(8): Show | 11 | HG02630.hp1 HG03041.hp1 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+1146dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504238 | |||||
| chr16:504249
|
T | TCCTCCTG others(48): Show |
1 | a0002c0003t0002g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1395+1159_1395+116 others(59): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(145): Show |
2 | a0001c0002t0002g0158a0001c0002t0002g0171 | 2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1395+1159_1395+116 others(156): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(47): Show |
9 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+1159_1395+116 others(58): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(68): Show |
1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(550): Show |
1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(561): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(68): Show |
2 | a0001c0001t0005g0066a0001c0001t0014g0177 | 2 | HG00558.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(852): Show |
3 | a0001c0002t0005g0070a0001c0002t0005g0075a0001c0002t0005g0079 | 3 | HG00323.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(863): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(525): Show |
1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(536): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(183): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(194): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(67): Show |
70 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(78): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(649): Show |
1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(660): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(182): Show |
1 | a0001c0002t0009g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(193): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(87): Show |
3 | a0001c0002t0019g0106a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1395+1186_1395+118 others(98): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCCTCCTG others(202): Show |
1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+1186_1395+118 others(213): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCTTCCTG others(141): Show |
2 | a0001c0001t0015g0123a0001c0001t0015g0127 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1395+1153_1395+115 others(152): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504249
|
T | TCTTCCTG others(68): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1395+1153_1395+115 others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504249 | |||||
| chr16:504258
|
A | AC | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+1166dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504258 | |||||
| chr16:504258
|
A | ACCCCCTC others(203): Show |
1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(214): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504258 | |||||
| chr16:504258
|
A | ACCCCCTC others(88): Show |
3 | a0001c0001t0003g0076a0001c0001t0008g0071a0001c0001t0008g0077 | 3 | HG02559.hp1 HG02738.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(99): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504258 | |||||
| chr16:504258
|
A | ACCCCCTC others(109): Show |
2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(120): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504258 | |||||
| chr16:504269
|
T | TCCTCCTG others(275): Show |
6 | a0001c0001t0015g0122a0001c0001t0015g0184a0001c0001t0024g0185others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(286): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(294): Show |
1 | a0001c0001t0010g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(305): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(179): Show |
1 | a0001c0001t0001g0259 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(190): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(178): Show |
12 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(9): Show | 12 | HG00673.hp1 HG01361.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(189): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(294): Show |
1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(305): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(237): Show |
9 | a0001c0001t0008g0294a0001c0001t0013g0026a0001c0001t0013g0027others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+1179_1395+118 others(248): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(352): Show |
1 | a0004c0007t0022g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(363): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(182): Show |
1 | a0001c0002t0009g0275 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(193): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504269
|
T | TCCTCCTG others(216): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1395+1179_1395+118 others(227): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504269 | |||||
| chr16:504277
|
T | C | 150 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1395+1180T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504277 | ||||||
| chr16:504279
|
C | CTCCCATC others(276): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(287): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(67): Show |
133 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1395+1182_1395+118 others(78): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(87): Show |
1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(98): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(950): Show |
1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(961): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(182): Show |
2 | a0001c0001t0006g0243a0001c0001t0012g0226 | 2 | HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1395+1182_1395+118 others(193): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(602): Show |
1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(613): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(508): Show |
1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(519): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(737): Show |
1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(748): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(831): Show |
1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(842): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(736): Show |
2 | a0001c0002t0002g0141a0001c0002t0016g0156 | 2 | HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1395+1182_1395+118 others(747): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(622): Show |
3 | a0001c0002t0002g0146a0001c0002t0002g0152a0006c0010t0005g0080 | 3 | HG00323.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1395+1182_1395+118 others(633): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(66): Show |
1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(77): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504279
|
C | CTCCCATC others(87): Show |
1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1395+1182_1395+118 others(98): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504279 | ||||||
| chr16:504280
|
C | T | 1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1395+1183C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504280 | ||||||
| chr16:504282
|
C | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1395+1185C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504282 | ||||||
| chr16:504288
|
C | T | 1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1395+1191C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504288 | ||||||
| chr16:504292
|
C | T | 7 | a0001c0001t0002g0002a0001c0001t0014g0177a0001c0002t0005g0070others(4): Show | 7 | HG00323.hp1 HG01258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+1195C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504292 | ||||||
| chr16:504297
|
G | A | 1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1395+1200G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504297 | ||||||
| chr16:504302
|
C | CG | 40 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(37): Show | 40 | HG00323.hp1 HG00673.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1395+1205_1395+120 others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504302 | ||||||
| chr16:504318
|
C | T | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1206C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504318 | ||||||
| chr16:504321
|
T | C | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1203T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504321 | ||||||
| chr16:504323
|
C | CCT | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1200_1396-119 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504323 | |||||
| chr16:504326
|
T | C | 5 | a0001c0001t0008g0063a0001c0001t0008g0065a0001c0001t0008g0068others(2): Show | 5 | NA18967.hp2 NA18984.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1198T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504326 | ||||||
| chr16:504344
|
T | C | 291 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1396-1180T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504344 | ||||||
| chr16:504346
|
C | G | 1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1396-1178C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504346 | ||||||
| chr16:504356
|
C | T | 1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1396-1168C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504356 | ||||||
| chr16:504357
|
A | AC | 23 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(20): Show | 23 | HG00673.hp1 HG01167.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1396-1163dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504357 | |||||
| chr16:504358
|
C | A | 1 | a0001c0001t0010g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1396-1166C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504358 | ||||||
| chr16:504362
|
T | C | 3 | a0001c0001t0025g0021a0001c0006t0058g0111a0001c0012t0059g0107 | 3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1396-1162T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504362 | ||||||
| chr16:504373
|
A | AC | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-1146dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504373 | |||||
| chr16:504378
|
C | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1396-1146C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504378 | ||||||
| chr16:504393
|
A | ACCCCCTC others(14): Show |
2 | a0001c0002t0009g0041a0001c0002t0009g0275 | 2 | HG06807.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1396-1126_1396-112 others(25): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504393 | |||||
| chr16:504393
|
AC | A | 19 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(16): Show | 19 | HG00323.hp1 HG00673.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1396-1125delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504393 | |||||
| chr16:504394
|
C | CCCCCCCA others(403): Show |
1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1396-1125_1396-112 others(414): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTC others(13): Show |
4 | a0001c0001t0008g0063a0001c0001t0008g0068a0001c0001t0011g0179others(1): Show | 4 | NA18967.hp2 NA19004.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1118_1396-111 others(24): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTC others(172): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1396-1118_1396-111 others(183): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTC others(51): Show |
1 | a0001c0001t0008g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1396-1118_1396-111 others(62): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTT others(493): Show |
1 | a0001c0001t0029g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1396-1124_1396-112 others(504): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTT others(333): Show |
1 | a0001c0001t0003g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1396-1124_1396-112 others(344): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCCTT others(492): Show |
2 | a0001c0001t0008g0071a0001c0001t0008g0077 | 2 | HG02738.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1396-1124_1396-112 others(503): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504394
|
C | CCCCCTCA others(27): Show |
3 | a0001c0001t0011g0110a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG01891.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1396-1126_1396-112 others(38): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504394 | |||||
| chr16:504397
|
C | CCCCTCAC others(126): Show |
1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1396-1125_1396-112 others(137): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504397 | |||||
| chr16:504397
|
C | CCCTCACC others(222): Show |
1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1396-1118_1396-111 others(233): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504397 | |||||
| chr16:504397
|
C | CCCTTGCC others(218): Show |
1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1396-1124_1396-112 others(229): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504397 | |||||
| chr16:504397
|
C | G | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-1127C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504397 | ||||||
| chr16:504407
|
T | C | 122 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(119): Show | 123 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-1117T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504407 | ||||||
| chr16:504407
|
T | TTCCTGTA others(8): Show |
1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(125): Show |
2 | a0001c0001t0001g0266a0001c0001t0018g0043 | 2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(136): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(14): Show |
39 | a0001c0001t0001g0234a0001c0001t0001g0283a0001c0001t0002g0005others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(25): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(228): Show |
1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(239): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(568): Show |
5 | a0001c0002t0002g0121a0001c0002t0002g0154a0001c0002t0002g0167others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(579): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(684): Show |
3 | a0001c0002t0002g0149a0001c0002t0030g0147a0008c0016t0002g0114 | 3 | HG01346.hp1 HG01978.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(695): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(796): Show |
1 | a0001c0002t0002g0153 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(807): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(460): Show |
1 | a0001c0001t0002g0002 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(471): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(458): Show |
1 | a0001c0019t0002g0012 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(469): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(130): Show |
2 | a0001c0002t0002g0146a0001c0002t0002g0152 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(141): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504407
|
T | TTCCTGTA others(129): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(140): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504407 | |||||
| chr16:504410
|
C | CTGTACCA others(28): Show |
1 | a0001c0001t0011g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(39): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504410 | |||||
| chr16:504410
|
C | T | 3 | a0001c0001t0011g0110a0001c0001t0011g0257a0001c0001t0011g0258 | 3 | HG01891.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1396-1114C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504410 | ||||||
| chr16:504412
|
G | GTACCACC others(222): Show |
1 | a0001c0001t0006g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(233): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(127): Show |
1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(138): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(186): Show |
1 | a0002c0003t0002g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(197): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(454): Show |
1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(465): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(282): Show |
4 | a0001c0001t0006g0196a0001c0001t0006g0207a0001c0001t0006g0238others(1): Show | 4 | HG01346.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(293): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(242): Show |
2 | a0001c0001t0025g0109a0001c0008t0057g0113 | 2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(253): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(202): Show |
1 | a0001c0001t0014g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(213): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(243): Show |
3 | a0001c0001t0018g0044a0001c0001t0035g0045a0002c0003t0018g0101 | 3 | HG02109.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(254): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(283): Show |
1 | a0001c0001t0033g0128 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(294): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(222): Show |
75 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(233): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(244): Show |
5 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0253others(2): Show | 5 | HG01243.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(255): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(551): Show |
1 | a0001c0001t0001g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(562): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCACC others(222): Show |
5 | a0001c0001t0001g0204a0001c0001t0001g0240a0001c0001t0001g0245others(2): Show | 5 | HG00423.hp1 HG00597.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(233): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCCGC others(470): Show |
1 | a0001c0001t0016g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(481): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCCTT others(249): Show |
1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(260): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCCTT others(248): Show |
5 | a0001c0002t0009g0081a0001c0002t0009g0254a0001c0002t0009g0269others(2): Show | 5 | HG01261.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-1112_1396-111 others(259): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504412
|
G | GTACCCTT others(246): Show |
1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1396-1112_1396-111 others(257): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504412 | ||||||
| chr16:504413
|
C | T | 98 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(95): Show | 99 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1396-1111C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504413 | ||||||
| chr16:504414
|
A | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1396-1110A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504414 | ||||||
| chr16:504416
|
T | C | 211 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(208): Show | 212 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1396-1108T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504416 | ||||||
| chr16:504417
|
C | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1396-1107C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504417 | ||||||
| chr16:504418
|
C | CCCTCACC others(57): Show |
7 | a0001c0001t0008g0294a0001c0001t0015g0123a0001c0001t0015g0127others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(68): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCCTCACC others(57): Show |
4 | a0001c0001t0015g0122a0001c0001t0041g0126a0001c0001t0056g0124others(1): Show | 4 | HG02895.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(68): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCCTCACC others(16): Show |
1 | a0005c0017t0037g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(27): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCCTCACC others(639): Show |
1 | a0001c0002t0043g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(650): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCCTCACC others(659): Show |
1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(670): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCCTCACC others(639): Show |
1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(650): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCT | 18 | a0001c0001t0001g0159a0001c0001t0001g0200a0001c0001t0001g0203others(15): Show | 18 | HG00673.hp1 HG01167.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(6): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(617): Show |
1 | a0001c0001t0024g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(628): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(357): Show |
2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(368): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(337): Show |
2 | a0001c0001t0006g0225a0001c0001t0010g0194 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(348): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(253): Show |
1 | a0001c0001t0003g0211 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(264): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(15): Show |
1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(26): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(252): Show |
1 | a0001c0001t0003g0213 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(263): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(75): Show |
1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(86): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(133): Show |
1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(144): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(251): Show |
1 | a0001c0001t0003g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(262): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(271): Show |
34 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0235others(31): Show | 34 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(282): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(291): Show |
3 | a0001c0001t0011g0084a0001c0001t0040g0083a0001c0001t0042g0085 | 3 | HG01109.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(302): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(311): Show |
1 | a0001c0001t0004g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(322): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(113): Show |
1 | a0001c0001t0003g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(124): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(601): Show |
1 | a0001c0001t0003g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(612): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(581): Show |
1 | a0001c0001t0003g0260 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(592): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(600): Show |
1 | a0001c0001t0003g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(611): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(231): Show |
1 | a0001c0001t0046g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1396-1105_1396-110 others(242): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(251): Show |
7 | a0001c0001t0003g0133a0001c0001t0003g0135a0001c0001t0003g0209others(4): Show | 7 | HG02735.hp2 NA18943.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(262): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | CCTCACCT others(602): Show |
3 | a0001c0001t0003g0216a0001c0001t0007g0134a0001c0001t0011g0132 | 3 | HG02027.hp2 HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1396-1105_1396-110 others(613): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504418 | |||||
| chr16:504418
|
C | T | 109 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1396-1106C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504418 | ||||||
| chr16:504420
|
A | C | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1104A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504420 | ||||||
| chr16:504421
|
T | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(205): Show | 209 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1396-1103T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504421 | ||||||
| chr16:504422
|
C | T | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1102C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504422 | ||||||
| chr16:504423
|
T | G | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1101T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504423 | ||||||
| chr16:504439
|
C | T | 9 | a0001c0001t0003g0076a0001c0001t0008g0063a0001c0001t0008g0065others(6): Show | 9 | HG02559.hp1 HG02738.hp2 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-1085C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504439 | ||||||
| chr16:504446
|
T | TCCTGTAC others(205): Show |
1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1396-1078_1396-107 others(216): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504446 | ||||||
| chr16:504447
|
T | C | 1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1396-1077T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504447 | ||||||
| chr16:504448
|
G | C | 1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1396-1076G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504448 | ||||||
| chr16:504450
|
G | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1396-1074G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504450 | ||||||
| chr16:504451
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1396-1073C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504451 | ||||||
| chr16:504452
|
A | AC | 9 | a0001c0001t0004g0074a0001c0001t0006g0272a0001c0001t0007g0082others(6): Show | 9 | HG01891.hp1 HG02074.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-1068dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504452 | |||||
| chr16:504452
|
A | ACCCCCTC others(91): Show |
1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1396-1068_1396-106 others(102): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504452 | |||||
| chr16:504453
|
C | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1396-1071C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504453 | ||||||
| chr16:504453
|
C | CCCCCTCA others(609): Show |
1 | a0001c0002t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1396-1068_1396-106 others(620): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504453 | |||||
| chr16:504453
|
C | CCCCTCAC others(547): Show |
1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1396-1031_1396-103 others(558): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504453 | |||||
| chr16:504459
|
A | ACCTCCTG others(213): Show |
1 | a0001c0001t0018g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1396-1023_1396-102 others(224): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504459 | |||||
| chr16:504459
|
A | ACCTCCTG others(130): Show |
1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1396-1031_1396-103 others(141): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504459 | |||||
| chr16:504461
|
C | CTCCTGTA others(74): Show |
1 | a0001c0001t0008g0068 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1396-1031_1396-103 others(85): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504461 | |||||
| chr16:504468
|
A | ACCCCCTC others(35): Show |
1 | a0001c0002t0019g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1396-1031_1396-103 others(46): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504468 | |||||
| chr16:504477
|
C | CCTCCTCC others(429): Show |
1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1396-1023_1396-102 others(440): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504477 | |||||
| chr16:504488
|
AC | A | 6 | a0001c0001t0001g0278a0001c0001t0008g0065a0001c0002t0019g0037others(3): Show | 6 | HG01106.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-1030delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504488 | |||||
| chr16:504489
|
C | T | 1 | a0001c0001t0005g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1396-1035C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504489 | ||||||
| chr16:504502
|
T | C | 229 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(226): Show | 230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1396-1022T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504502 | ||||||
| chr16:504502
|
T | TTCCTGTA others(317): Show |
1 | a0002c0003t0002g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1396-1013_1396-101 others(328): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(320): Show |
1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1396-1013_1396-101 others(331): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(417): Show |
1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1396-1013_1396-101 others(428): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(377): Show |
21 | a0001c0002t0002g0121a0001c0002t0002g0141a0001c0002t0002g0146others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1396-1013_1396-101 others(388): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(317): Show |
25 | a0001c0001t0001g0234a0001c0001t0002g0005a0001c0001t0002g0008others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.1396-1013_1396-101 others(328): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(569): Show |
2 | a0001c0001t0014g0142a0001c0001t0014g0143 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1396-1013_1396-101 others(580): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(663): Show |
1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1396-1013_1396-101 others(674): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(317): Show |
1 | a0002c0003t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1396-1013_1396-101 others(328): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(297): Show |
2 | a0001c0001t0002g0174a0001c0001t0002g0176 | 2 | HG01981.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1396-1013_1396-101 others(308): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504502
|
T | TTCCTGTA others(493): Show |
1 | a0001c0002t0002g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1396-1012_1396-101 others(504): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504502 | |||||
| chr16:504504
|
C | T | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1020C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504504 | ||||||
| chr16:504509
|
A | ACCCCCCT others(370): Show |
6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-1010_1396-100 others(381): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504509 | |||||
| chr16:504509
|
A | ACCCCCCT others(97): Show |
1 | a0001c0001t0015g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1396-1010_1396-100 others(108): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504509 | |||||
| chr16:504509
|
A | ACCCCCTC others(35): Show |
1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1396-997_1396-996i others(44): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504509 | |||||
| chr16:504509
|
A | ACCCCCTC others(96): Show |
8 | a0001c0001t0003g0076a0001c0001t0008g0063a0001c0001t0008g0065others(5): Show | 8 | HG02559.hp1 HG02738.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-997_1396-996i others(105): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504509 | |||||
| chr16:504511
|
C | T | 2 | a0001c0002t0053g0271a0001c0002t0054g0267 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1396-1013C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504511 | ||||||
| chr16:504554
|
C | T | 292 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1396-970C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504554 | ||||||
| chr16:504567
|
ACCCCTCA others(10): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1396-943_1396-927d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504567 | |||||
| chr16:504569
|
C | A | 5 | a0001c0001t0001g0214a0001c0001t0001g0230a0001c0001t0001g0262others(2): Show | 5 | HG00408.hp2 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-955C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504569 | ||||||
| chr16:504574
|
A | ACCTCCTG others(13): Show |
7 | a0001c0002t0009g0081a0001c0002t0009g0254a0001c0002t0009g0269others(4): Show | 7 | HG01261.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1396-935_1396-916d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504574 | |||||
| chr16:504574
|
A | ACCTCCTG others(71): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0165 | 2 | NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1396-916_1396-915i others(80): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504574 | |||||
| chr16:504588
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1396-936C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504588 | ||||||
| chr16:504603
|
A | ACCCCCTC others(14): Show |
1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1396-916_1396-915i others(23): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504603 | |||||
| chr16:504617
|
TTCCTGTA others(70): Show |
T | 2 | a0001c0001t0011g0257a0001c0001t0011g0258 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1396-897_1396-821d others(79): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504617 | |||||
| chr16:504624
|
A | AC | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-897dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504624 | |||||
| chr16:504628
|
T | C | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-896T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504628 | ||||||
| chr16:504633
|
T | C | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-891T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504633 | ||||||
| chr16:504634
|
T | G | 1 | a0001c0002t0002g0167 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1396-890T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504634 | ||||||
| chr16:504634
|
TCCTCCTG others(31): Show |
T | 2 | a0001c0001t0011g0110a0001c0001t0011g0256 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1396-862_1396-825d others(40): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504634 | |||||
| chr16:504643
|
A | AC | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-876dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504643 | |||||
| chr16:504662
|
C | T | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-862C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504662 | ||||||
| chr16:504663
|
AC | A | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-855delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504663 | |||||
| chr16:504671
|
T | C | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-853T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504671 | ||||||
| chr16:504672
|
ACCTCCTG others(13): Show |
A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1396-840_1396-821d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504672 | |||||
| chr16:504674
|
C | CTCT | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-848_1396-847i others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504674 | |||||
| chr16:504684
|
CCCTCACC others(13): Show |
C | 3 | a0001c0001t0001g0200a0001c0001t0001g0251a0001c0001t0015g0136 | 3 | HG01361.hp2 HG02572.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1396-825_1396-806d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504684 | |||||
| chr16:504692
|
T | TCCTCCTG others(188): Show |
1 | a0001c0001t0015g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1396-821_1396-820i others(197): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504692 | |||||
| chr16:504692
|
T | TCCTCCTG others(405): Show |
1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1396-821_1396-820i others(414): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504692 | |||||
| chr16:504692
|
T | TCCTCCTG others(187): Show |
7 | a0001c0001t0015g0123a0001c0001t0015g0127a0001c0001t0024g0129others(4): Show | 7 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1396-821_1396-820i others(196): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504692 | |||||
| chr16:504699
|
GTACCGCC others(13): Show |
G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1396-820_1396-801d others(22): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504699 | |||||
| chr16:504703
|
C | CGCCTCAC others(406): Show |
1 | a0001c0001t0001g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1396-709_1396-708i others(415): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504703 | |||||
| chr16:504703
|
C | T | 52 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(49): Show | 52 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1396-821C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504703 | ||||||
| chr16:504704
|
G | C | 9 | a0001c0001t0015g0122a0001c0001t0015g0123a0001c0001t0015g0127others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1396-820G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504704 | ||||||
| chr16:504713
|
C | T | 5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0033g0128others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-811C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504713 | ||||||
| chr16:504759
|
G | A | 1 | a0001c0004t0003g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1396-765G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504759 | ||||||
| chr16:504781
|
C | T | 2 | a0001c0001t0020g0247a0007c0015t0020g0199 | 2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1396-743C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 504781 | ||||||
| chr16:504810
|
CCTCCTGT others(10): Show |
C | 1 | a0002c0003t0002g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1396-699_1396-683d others(19): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 504810 | |||||
| chr16:505030
|
C | G | 5 | a0001c0001t0008g0294a0002c0003t0011g0102a0004c0007t0022g0067others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-494C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 505030 | ||||||
| chr16:505159
|
A | G | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1396-365A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 505159 | ||||||
| chr16:505345
|
C | T | 2 | a0001c0002t0002g0149a0001c0002t0002g0167 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1396-179C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 505345 | ||||||
| chr16:505505
|
G | T | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1396-19G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 7/13 | chr16 | 505505 | ||||||
| chr16:505708
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1499+81C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 505708 | ||||||
| chr16:505734
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1499+107G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 505734 | ||||||
| chr16:505795
|
G | A | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1499+168G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 505795 | ||||||
| chr16:505801
|
T | A | 1 | a0001c0002t0009g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1499+174T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 505801 | ||||||
| chr16:505816
|
C | T | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1499+189C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 505816 | ||||||
| chr16:506000
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1499+373G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506000 | ||||||
| chr16:506202
|
C | T | 5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0033g0128others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499+575C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506202 | ||||||
| chr16:506298
|
G | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0160others(3): Show | 6 | NA18944.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+671G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506298 | ||||||
| chr16:506375
|
G | A | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1499+748G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506375 | ||||||
| chr16:506532
|
C | T | 1 | a0001c0002t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1499+905C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506532 | ||||||
| chr16:506589
|
A | C | 1 | a0001c0001t0007g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1499+962A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506589 | ||||||
| chr16:506787
|
G | A | 2 | a0001c0001t0014g0142a0001c0001t0014g0143 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1499+1160G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506787 | ||||||
| chr16:506801
|
T | C | 69 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(66): Show | 70 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1499+1174T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506801 | ||||||
| chr16:506881
|
G | A | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1499+1254G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 506881 | ||||||
| chr16:507112
|
C | CT | 19 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0277others(16): Show | 19 | HG00323.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1499+1503dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 507112 | |||||
| chr16:507112
|
CT | C | 25 | a0001c0001t0003g0133a0001c0001t0003g0135a0001c0001t0003g0202others(22): Show | 25 | HG00609.hp1 HG01074.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1499+1503delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 507112 | |||||
| chr16:507134
|
AC | A | 3 | a0003c0005t0014g0022a0003c0005t0014g0023a0003c0005t0014g0024 | 3 | HG03453.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1499+1508delC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507134 | ||||||
| chr16:507188
|
C | T | 107 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0159others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1499+1561C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507188 | ||||||
| chr16:507269
|
C | T | 2 | a0001c0002t0053g0271a0001c0002t0054g0267 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1499+1642C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507269 | ||||||
| chr16:507399
|
C | T | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1499+1772C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507399 | ||||||
| chr16:507407
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499+1780G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507407 | ||||||
| chr16:507527
|
G | T | 25 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0159others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1499+1900G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507527 | ||||||
| chr16:507641
|
G | A | 1 | a0001c0002t0019g0106 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1499+2014G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507641 | ||||||
| chr16:507738
|
C | CACGTTTC others(74): Show |
56 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(53): Show | 56 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1499+2179_1499+218 others(85): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 507738 | |||||
| chr16:507738
|
CACGTTTC others(74): Show |
C | 1 | a0001c0001t0005g0007 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1499+2246_1499+232 others(85): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 507738 | |||||
| chr16:507985
|
G | A | 1 | a0001c0001t0047g0139 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1499+2358G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 507985 | ||||||
| chr16:508009
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1499+2382C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508009 | ||||||
| chr16:508021
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1499+2394G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508021 | ||||||
| chr16:508449
|
C | T | 15 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(12): Show | 15 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1500-2211C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508449 | ||||||
| chr16:508669
|
T | C | 18 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1500-1991T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508669 | ||||||
| chr16:508685
|
C | T | 2 | a0001c0002t0002g0157a0001c0002t0002g0250 | 2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1500-1975C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508685 | ||||||
| chr16:508788
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1500-1872C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508788 | ||||||
| chr16:508793
|
G | A | 1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1500-1867G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508793 | ||||||
| chr16:508822
|
A | T | 1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1500-1838A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 508822 | ||||||
| chr16:508907
|
C | CT | 6 | a0001c0001t0003g0213a0001c0001t0004g0074a0001c0001t0010g0004others(3): Show | 7 | HG00423.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1500-1739dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 508907 | |||||
| chr16:509087
|
A | G | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-1573A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509087 | ||||||
| chr16:509201
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1500-1459A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509201 | ||||||
| chr16:509214
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1500-1446A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509214 | ||||||
| chr16:509312
|
G | A | 4 | a0001c0001t0011g0110a0001c0001t0011g0256a0001c0001t0011g0257others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-1348G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509312 | ||||||
| chr16:509505
|
G | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0213 | 2 | NA18939.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1500-1155G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509505 | ||||||
| chr16:509626
|
T | G | 1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1500-1034T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509626 | ||||||
| chr16:509720
|
C | A | 4 | a0001c0001t0001g0182a0001c0001t0006g0187a0001c0001t0010g0188others(1): Show | 4 | HG02886.hp2 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-940C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509720 | ||||||
| chr16:509746
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1500-914G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509746 | ||||||
| chr16:509750
|
G | GC | 49 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(46): Show | 49 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1500-900dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 509750 | |||||
| chr16:509760
|
C | A | 9 | a0001c0001t0002g0002a0001c0001t0010g0004a0001c0001t0016g0003others(6): Show | 9 | HG00423.hp2 HG01928.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1500-900C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509760 | ||||||
| chr16:509760
|
C | G | 2 | a0001c0001t0006g0243a0001c0001t0012g0226 | 2 | HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1500-900C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509760 | ||||||
| chr16:509791
|
G | A | 1 | a0001c0001t0048g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1500-869G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509791 | ||||||
| chr16:509796
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1500-864T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509796 | ||||||
| chr16:509859
|
C | T | 1 | a0001c0001t0011g0179 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1500-801C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 509859 | ||||||
| chr16:510001
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1500-659C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510001 | ||||||
| chr16:510037
|
C | CCCGTGCC others(209): Show |
4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(1): Show | 4 | HG00438.hp2 HG00597.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-580_1500-365d others(218): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 510037 | |||||
| chr16:510063
|
GCGTTGTG others(65): Show |
G | 21 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(18): Show | 21 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1500-525_1500-454d others(74): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 510063 | |||||
| chr16:510099
|
G | A | 26 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(23): Show | 26 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1500-561G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510099 | ||||||
| chr16:510111
|
C | T | 1 | a0001c0001t0011g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1500-549C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510111 | ||||||
| chr16:510181
|
CCCGTGCC others(65): Show |
C | 1 | a0001c0001t0007g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1500-436_1500-365d others(74): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 510181 | |||||
| chr16:510202
|
C | T | 1 | a0001c0001t0061g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1500-458C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510202 | ||||||
| chr16:510231
|
C | T | 3 | a0001c0002t0019g0106a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1500-429C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510231 | ||||||
| chr16:510253
|
T | C | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1500-407T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510253 | ||||||
| chr16:510274
|
C | T | 20 | a0001c0001t0015g0039a0001c0002t0009g0040a0001c0002t0009g0041others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1500-386C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510274 | ||||||
| chr16:510441
|
C | T | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1500-219C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510441 | ||||||
| chr16:510495
|
G | A | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1500-165G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510495 | ||||||
| chr16:510525
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0010g0195 | 2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1500-135G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510525 | ||||||
| chr16:510652
|
C | T | 1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.1500-8C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 8/13 | chr16 | 510652 | ||||||
| chr16:510824
|
C | T | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1640+24C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 510824 | ||||||
| chr16:510962
|
A | C | 125 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(122): Show | 126 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1640+162A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 510962 | ||||||
| chr16:510965
|
T | C | 125 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(122): Show | 126 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1640+165T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 510965 | ||||||
| chr16:511017
|
G | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640+217G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511017 | ||||||
| chr16:511035
|
CGGCCAGG others(42): Show |
C | 15 | a0001c0001t0008g0294a0001c0001t0015g0039a0001c0001t0015g0122others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1640+348_1640+396d others(51): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511035 | |||||
| chr16:511039
|
C | CAGGTAGG others(380): Show |
11 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(8): Show | 11 | HG01070.hp2 HG02074.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1640+347_1640+348i others(389): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511039 | |||||
| chr16:511076
|
G | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1640+276G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511076 | ||||||
| chr16:511190
|
T | C | 1 | a0001c0004t0003g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1640+390T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511190 | ||||||
| chr16:511255
|
A | G | 4 | a0001c0002t0002g0146a0001c0002t0002g0152a0001c0014t0039g0112others(1): Show | 4 | HG00323.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640+455A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511255 | ||||||
| chr16:511259
|
T | C | 3 | a0001c0001t0025g0021a0001c0001t0025g0109a0001c0008t0057g0113 | 3 | HG02257.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1640+459T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511259 | ||||||
| chr16:511351
|
G | GGCCCGCC others(41): Show |
16 | a0001c0002t0009g0040a0001c0002t0009g0041a0001c0002t0009g0081others(13): Show | 16 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1640+559_1640+606d others(50): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511351 | |||||
| chr16:511351
|
G | GGCCCGCC others(233): Show |
3 | a0001c0002t0019g0106a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1640+606_1640+607i others(242): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511351 | |||||
| chr16:511399
|
A | G | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1640+599A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511399 | ||||||
| chr16:511447
|
C | A | 1 | a0001c0008t0057g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1640+647C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511447 | ||||||
| chr16:511452
|
C | T | 1 | a0001c0001t0008g0148 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1640+652C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511452 | ||||||
| chr16:511453
|
G | T | 3 | a0001c0002t0005g0070a0001c0002t0005g0075a0001c0002t0005g0079 | 3 | HG00323.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1640+653G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511453 | ||||||
| chr16:511457
|
A | C | 1 | a0001c0002t0009g0284 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1640+657A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511457 | ||||||
| chr16:511471
|
C | A | 1 | a0001c0001t0002g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1640+671C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511471 | ||||||
| chr16:511475
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1640+675T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511475 | ||||||
| chr16:511475
|
TAGGTAGG others(42): Show |
T | 2 | a0001c0001t0004g0089a0001c0012t0059g0107 | 2 | HG00609.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1640+784_1640+832d others(51): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511475 | |||||
| chr16:511523
|
C | G | 12 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(9): Show | 13 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640+723C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511523 | ||||||
| chr16:511571
|
G | A | 1 | a0001c0001t0016g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1640+771G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511571 | ||||||
| chr16:511572
|
C | G | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640+772C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511572 | ||||||
| chr16:511592
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1640+792G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511592 | ||||||
| chr16:511599
|
C | T | 2 | a0001c0001t0011g0084a0001c0001t0041g0126 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1640+799C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511599 | ||||||
| chr16:511626
|
T | TAGGAGAG others(41): Show |
1 | a0001c0001t0002g0176 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1640+843_1640+890d others(50): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511626 | |||||
| chr16:511642
|
C | A | 1 | a0001c0004t0003g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1640+842C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511642 | ||||||
| chr16:511714
|
A | C | 1 | a0001c0001t0036g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1640+914A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511714 | ||||||
| chr16:511734
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1640+934T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511734 | ||||||
| chr16:511741
|
A | C | 125 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(122): Show | 126 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1640+941A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511741 | ||||||
| chr16:511930
|
G | A | 4 | a0001c0001t0015g0122a0001c0001t0015g0136a0001c0001t0056g0124others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1640+1130G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511930 | ||||||
| chr16:511933
|
G | GGCCCGCC others(137): Show |
1 | a0001c0001t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1640+1140_1640+114 others(148): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 511933 | |||||
| chr16:511938
|
G | A | 1 | a0001c0001t0034g0208 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1640+1138G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 511938 | ||||||
| chr16:512304
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1640+1504G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512304 | ||||||
| chr16:512353
|
G | A | 5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0033g0128others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+1553G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512353 | ||||||
| chr16:512365
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1640+1565C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512365 | ||||||
| chr16:512383
|
G | C | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640+1583G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512383 | ||||||
| chr16:512417
|
A | T | 132 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(129): Show | 133 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1640+1617A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512417 | ||||||
| chr16:512481
|
C | T | 3 | a0001c0002t0002g0183a0001c0002t0002g0190a0001c0002t0002g0255 | 3 | HG00140.hp2 HG01192.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1640+1681C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512481 | ||||||
| chr16:512485
|
C | G | 1 | a0001c0001t0010g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1640+1685C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512485 | ||||||
| chr16:512539
|
C | CT | 19 | a0001c0001t0001g0117a0001c0001t0001g0215a0001c0001t0001g0259others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1640+1761dupT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 512539 | |||||
| chr16:512539
|
CT | C | 31 | a0001c0001t0001g0115a0001c0001t0001g0144a0001c0001t0001g0206others(28): Show | 31 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1640+1761delT | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 512539 | |||||
| chr16:512638
|
C | G | 125 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(122): Show | 126 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.1640+1838C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512638 | ||||||
| chr16:512695
|
C | A | 3 | a0001c0002t0019g0106a0001c0002t0019g0285a0001c0002t0043g0025 | 3 | HG01106.hp1 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1640+1895C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512695 | ||||||
| chr16:512918
|
G | A | 1 | a0001c0001t0006g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1640+2118G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512918 | ||||||
| chr16:512967
|
C | G | 1 | a0001c0001t0012g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1640+2167C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 512967 | ||||||
| chr16:513180
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1640+2380G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513180 | ||||||
| chr16:513307
|
A | C | 1 | a0001c0002t0002g0153 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1640+2507A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513307 | ||||||
| chr16:513313
|
C | T | 1 | a0001c0001t0006g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1640+2513C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513313 | ||||||
| chr16:513371
|
T | C | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1640+2571T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513371 | ||||||
| chr16:513673
|
T | C | 1 | a0001c0001t0004g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1640+2873T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513673 | ||||||
| chr16:513856
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1640+3056G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513856 | ||||||
| chr16:513922
|
A | G | 55 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(52): Show | 55 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1640+3122A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513922 | ||||||
| chr16:513936
|
G | A | 14 | a0001c0002t0009g0040a0001c0002t0009g0041a0001c0002t0009g0081others(11): Show | 14 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1640+3136G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 513936 | ||||||
| chr16:514091
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1640+3291A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 514091 | ||||||
| chr16:514224
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1640+3424C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 514224 | ||||||
| chr16:514504
|
G | T | 1 | a0001c0006t0058g0111 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1640+3704G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 514504 | ||||||
| chr16:514881
|
C | T | 3 | a0001c0001t0003g0180a0001c0001t0003g0213a0001c0001t0007g0053 | 3 | HG00544.hp1 NA18939.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1641-4062C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 514881 | ||||||
| chr16:514883
|
G | C | 1 | a0001c0002t0054g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1641-4060G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 514883 | ||||||
| chr16:515318
|
T | C | 5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0033g0128others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1641-3625T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515318 | ||||||
| chr16:515371
|
G | A | 26 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(23): Show | 26 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1641-3572G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515371 | ||||||
| chr16:515479
|
T | TGGCTGAC others(116): Show |
1 | a0001c0001t0004g0178 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1641-3413_1641-329 others(127): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 515479 | |||||
| chr16:515500
|
C | CGCATCTC others(157): Show |
5 | a0001c0001t0018g0043a0001c0001t0018g0044a0001c0001t0033g0128others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1641-3395_1641-323 others(168): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 515500 | |||||
| chr16:515516
|
C | T | 7 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1641-3427C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515516 | ||||||
| chr16:515561
|
C | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0117others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1641-3382C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515561 | ||||||
| chr16:515616
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0235 | 2 | NA18955.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1641-3327C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515616 | ||||||
| chr16:515657
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1641-3286C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515657 | ||||||
| chr16:515736
|
T | G | 1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1641-3207T>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515736 | ||||||
| chr16:515737
|
G | A | 1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1641-3206G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515737 | ||||||
| chr16:515738
|
T | C | 1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1641-3205T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515738 | ||||||
| chr16:515739
|
T | C | 1 | a0001c0001t0008g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1641-3204T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515739 | ||||||
| chr16:515768
|
G | A | 7 | a0001c0001t0010g0032a0001c0001t0010g0046a0001c0001t0012g0030others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1641-3175G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515768 | ||||||
| chr16:515958
|
C | T | 1 | a0001c0001t0003g0135 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1641-2985C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515958 | ||||||
| chr16:515963
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0006g0187a0001c0001t0010g0188others(1): Show | 4 | HG02886.hp2 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1641-2980G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515963 | ||||||
| chr16:515970
|
C | T | 1 | a0001c0004t0011g0062 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1641-2973C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 515970 | ||||||
| chr16:516293
|
G | A | 1 | a0008c0016t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1641-2650G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516293 | ||||||
| chr16:516740
|
G | T | 1 | a0001c0001t0012g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1641-2203G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516740 | ||||||
| chr16:516797
|
A | C | 1 | a0001c0001t0015g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1641-2146A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516797 | ||||||
| chr16:516945
|
C | T | 94 | a0001c0001t0001g0266a0001c0001t0003g0060a0001c0001t0003g0125others(91): Show | 95 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1641-1998C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516945 | ||||||
| chr16:516945
|
CGGGGGCT others(60): Show |
C | 1 | a0001c0001t0051g0064 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1641-1996_1641-193 others(71): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 516945 | |||||
| chr16:516948
|
G | A | 1 | a0001c0001t0031g0166 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1641-1995G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516948 | ||||||
| chr16:516960
|
G | A | 1 | a0001c0001t0005g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1641-1983G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 516960 | ||||||
| chr16:517043
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1641-1900G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517043 | ||||||
| chr16:517055
|
G | A | 1 | a0001c0001t0028g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1641-1888G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517055 | ||||||
| chr16:517086
|
C | T | 26 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(23): Show | 26 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1641-1857C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517086 | ||||||
| chr16:517170
|
G | A | 1 | a0001c0001t0020g0236 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1641-1773G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517170 | ||||||
| chr16:517258
|
A | G | 2 | a0001c0001t0025g0109a0001c0008t0057g0113 | 2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1641-1685A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517258 | ||||||
| chr16:517387
|
G | A | 2 | a0001c0001t0015g0123a0001c0001t0015g0127 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1641-1556G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517387 | ||||||
| chr16:517395
|
T | C | 134 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(131): Show | 135 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1641-1548T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517395 | ||||||
| chr16:517620
|
C | T | 1 | a0001c0001t0011g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1641-1323C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517620 | ||||||
| chr16:517812
|
G | T | 1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1641-1131G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517812 | ||||||
| chr16:517820
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1641-1123C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517820 | ||||||
| chr16:517887
|
C | G | 1 | a0002c0018t0009g0092 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1641-1056C>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517887 | ||||||
| chr16:517975
|
G | C | 51 | a0001c0001t0003g0060a0001c0001t0003g0125a0001c0001t0003g0133others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1641-968G>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 517975 | ||||||
| chr16:518123
|
G | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1641-820G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518123 | ||||||
| chr16:518136
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1641-807T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518136 | ||||||
| chr16:518205
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1641-738A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518205 | ||||||
| chr16:518360
|
C | A | 2 | a0001c0001t0012g0189a0001c0001t0012g0280 | 2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1641-583C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518360 | ||||||
| chr16:518363
|
A | G | 20 | a0001c0002t0009g0040a0001c0002t0009g0041a0001c0002t0009g0081others(17): Show | 20 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1641-580A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518363 | ||||||
| chr16:518440
|
G | A | 2 | a0001c0002t0019g0285a0002c0003t0011g0102 | 2 | HG01106.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1641-503G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518440 | ||||||
| chr16:518485
|
GGGAGGCT others(126): Show |
G | 2 | a0001c0002t0053g0271a0001c0002t0054g0267 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1641-444_1641-312d others(2): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 518485 | |||||
| chr16:518502
|
G | A | 31 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(28): Show | 31 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1641-441G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518502 | ||||||
| chr16:518516
|
G | A | 11 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(8): Show | 11 | HG01070.hp2 HG02074.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1641-427G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518516 | ||||||
| chr16:518621
|
A | T | 1 | a0001c0002t0002g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1641-322A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518621 | ||||||
| chr16:518624
|
C | T | 6 | a0001c0001t0013g0026a0001c0001t0013g0027a0001c0001t0013g0028others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1641-319C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518624 | ||||||
| chr16:518701
|
G | T | 10 | a0001c0001t0015g0039a0001c0001t0015g0122a0001c0001t0015g0123others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1641-242G>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518701 | ||||||
| chr16:518703
|
T | A | 10 | a0001c0001t0015g0039a0001c0001t0015g0122a0001c0001t0015g0123others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1641-240T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518703 | ||||||
| chr16:518704
|
GACAGAGT | G | 10 | a0001c0001t0015g0039a0001c0001t0015g0122a0001c0001t0015g0123others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1641-238_1641-232d others(9): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518704 | ||||||
| chr16:518733
|
A | C | 1 | a0001c0001t0001g0239 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1641-210A>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518733 | ||||||
| chr16:518736
|
A | T | 1 | a0002c0003t0005g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1641-207A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518736 | ||||||
| chr16:518740
|
A | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1641-203A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518740 | ||||||
| chr16:518743
|
T | A | 1 | a0001c0012t0059g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1641-200T>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518743 | ||||||
| chr16:518745
|
ATAC | A | 17 | a0001c0002t0009g0040a0001c0002t0009g0041a0001c0002t0009g0081others(14): Show | 17 | HG01106.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1641-195_1641-193d others(5): Show |
RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 518745 | |||||
| chr16:518748
|
C | A | 115 | a0001c0001t0003g0060a0001c0001t0003g0076a0001c0001t0003g0125others(112): Show | 116 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.1641-195C>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518748 | ||||||
| chr16:518756
|
T | C | 1 | a0002c0003t0005g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1641-187T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518756 | ||||||
| chr16:518768
|
G | A | 1 | a0001c0014t0039g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1641-175G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | chr16 | 518768 | ||||||
| chr16:518886
|
TG | T | 2 | a0001c0001t0021g0001a0001c0006t0032g0270 | 3 | HG01069.hp1 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1641-55delG | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 518886 | |||||
| chr16:519086
|
C | T | 1 | a0001c0001t0040g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1722+62C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519086 | ||||||
| chr16:519118
|
G | A | 26 | a0001c0001t0003g0076a0001c0001t0004g0074a0001c0001t0008g0063others(23): Show | 26 | HG01070.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1722+94G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519118 | ||||||
| chr16:519193
|
A | T | 2 | a0001c0001t0015g0136a0001c0001t0056g0124 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1722+169A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519193 | ||||||
| chr16:519306
|
C | T | 4 | a0001c0002t0009g0274a0001c0002t0009g0275a0001c0002t0009g0284others(1): Show | 4 | NA18947.hp2 NA18955.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1722+282C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519306 | ||||||
| chr16:519386
|
G | A | 1 | a0001c0002t0019g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1722+362G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519386 | ||||||
| chr16:519416
|
A | G | 2 | a0001c0002t0002g0158a0001c0002t0002g0171 | 2 | HG01109.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1723-338A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519416 | ||||||
| chr16:519558
|
C | T | 2 | a0001c0002t0002g0183a0001c0002t0002g0190 | 2 | HG01192.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1723-196C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519558 | ||||||
| chr16:519636
|
C | T | 1 | a0002c0003t0011g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1723-118C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | chr16 | 519636 | ||||||
| chr16:519644
|
A | AC | 3 | a0001c0001t0001g0118a0001c0001t0007g0137a0001c0019t0002g0012 | 3 | NA18949.hp1 NA18950.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1723-108dupC | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr16 | 519644 | |||||
| chr16:519940
|
A | T | 1 | a0001c0004t0003g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1860+49A>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 11/13 | chr16 | 519940 | ||||||
| chr16:520012
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1861-110G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 11/13 | chr16 | 520012 | ||||||
| chr16:520070
|
G | A | 1 | a0001c0001t0045g0138 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1861-52G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 11/13 | chr16 | 520070 | ||||||
| chr16:520285
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0005g0013others(2): Show | 5 | NA18950.hp1 NA18967.hp1 NA18970.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2016+8G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 12/13 | chr16 | 520285 | ||||||
| chr16:520427
|
A | G | 5 | a0001c0001t0017g0049a0001c0001t0017g0057a0001c0001t0017g0061others(2): Show | 5 | HG01928.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017-32A>G | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 12/13 | chr16 | 520427 | ||||||
| chr16:520454
|
T | C | 249 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(246): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
splice_region_variant&intron_variant | LOW | c.2017-5T>C | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 12/13 | chr16 | 520454 | ||||||
| chr16:520623
|
G | A | 141 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0073others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2157+24G>A | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 13/13 | chr16 | 520623 | ||||||
| chr16:520720
|
C | T | 1 | a0001c0001t0025g0021 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2158-6C>T | RAB11FIP3 | ENSG00000090565.17 | transcript | ENST00000262305.9 | protein_coding | 13/13 | chr16 | 520720 |