Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 96459 |
|---|---|
| ensemblid | ENSG00000217128.13 |
| hgncid | 29418 |
| symbol | FNIP1 |
| name | folliculin interacting protein 1 |
| refseq_nuc | NM_133372.3 |
| refseq_prot | NP_588613.3 |
| ensembl_nuc | ENST00000510461.6 |
| ensembl_prot | ENSP00000421985.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 131641714 |
| end | 131797017 |
| strand | - |
| ver | v1.2 |
| region | chr5:131641714-131797017 |
| region5000 | chr5:131636714-131802017 |
| regionname0 | FNIP1_chr5_131641714_131797017 |
| regionname5000 | FNIP1_chr5_131636714_131802017 |
| 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 | 1166 | 254 | 67 | 53 | 116 | 3 | 14 | 101 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002 | 0/0 | 1166 | 53 | 6 | 11 | 27 | 1 | 8 | 21 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0003 | 0/0 | 1166 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0004 | 0/0 | 1166 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0005 | 0/0 | 1166 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0006 | 0/0 | 1166 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0007 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0008 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0009 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0010 | 1/0 | 1166 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| 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 | 0/1 | 3501 | 236 | 58 | 53 | 109 | 3 | 12 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0002 | 0/0 | 3501 | 50 | 6 | 8 | 27 | 1 | 8 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0003 | 0/0 | 3501 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0004 | 0/0 | 3501 | 6 | 0 | 0 | 5 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0005 | 0/0 | 3501 | 6 | 6 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0006 | 0/0 | 3501 | 3 | 0 | 3 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0007 | 0/0 | 3501 | 3 | 3 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0008 | 0/0 | 3501 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0009 | 0/0 | 3501 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0010 | 0/0 | 3501 | 2 | 0 | 0 | 0 | 0 | 2 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0011 | 1/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0012 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0013 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0014 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0015 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0016 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0017 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| c0018 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| 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 | 0/1 | 3067 | 128 | 27 | 28 | 59 | 2 | 11 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0002 | 1/0 | 3068 | 74 | 5 | 17 | 39 | 2 | 10 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0003 | 0/0 | 3067 | 29 | 21 | 8 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0004 | 0/0 | 3068 | 24 | 0 | 2 | 21 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0005 | 0/0 | 3069 | 21 | 5 | 5 | 10 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0006 | 0/0 | 3068 | 12 | 11 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0007 | 0/0 | 3068 | 9 | 2 | 0 | 7 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0008 | 0/0 | 3067 | 7 | 7 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0009 | 0/0 | 3066 | 5 | 4 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0010 | 0/0 | 3066 | 5 | 0 | 0 | 5 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0011 | 0/0 | 3069 | 2 | 0 | 1 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0012 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0013 | 0/0 | 3068 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0014 | 0/0 | 3066 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0015 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0016 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0017 | 0/0 | 3068 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0018 | 0/0 | 3068 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0019 | 0/0 | 3066 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0020 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0021 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0022 | 0/0 | 3067 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| t0023 | 0/0 | 3067 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| 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 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| 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 | 0/1 | 3501 | 236 | 58 | 53 | 109 | 3 | 12 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0004 | 0/0 | 3501 | 6 | 0 | 0 | 5 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0005 | 0/0 | 3501 | 6 | 6 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0008 | 0/0 | 3501 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0013 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0014 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0015 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0017 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002 | 0/0 | 3501 | 50 | 6 | 8 | 27 | 1 | 8 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0006 | 0/0 | 3501 | 3 | 0 | 3 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0003c0003 | 0/0 | 3501 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0004c0007 | 0/0 | 3501 | 3 | 3 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0005c0009 | 0/0 | 3501 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0006c0010 | 0/0 | 3501 | 2 | 0 | 0 | 0 | 0 | 2 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0007c0012 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0008c0016 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0009c0018 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0010c0011 | 1/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6567 | 109 | 18 | 28 | 53 | 2 | 7 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0002 | 0/0 | 6568 | 48 | 1 | 9 | 33 | 1 | 4 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0003 | 0/0 | 6567 | 28 | 20 | 8 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0005 | 0/0 | 6569 | 18 | 4 | 5 | 9 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0006 | 0/0 | 6568 | 2 | 1 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0007 | 0/0 | 6568 | 6 | 0 | 0 | 6 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0008 | 0/0 | 6567 | 7 | 7 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0009 | 0/0 | 6566 | 5 | 4 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0010 | 0/0 | 6566 | 5 | 0 | 0 | 5 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0012 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0013 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0016 | 0/0 | 6569 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0017 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0020 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0021 | 0/0 | 6569 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0022 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0001t0023 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0004t0001 | 0/0 | 6567 | 6 | 0 | 0 | 5 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0005t0001 | 0/0 | 6567 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0005t0007 | 0/0 | 6568 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0008t0002 | 0/0 | 6568 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0013t0001 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0014t0003 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0015t0001 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0001c0017t0001 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0002 | 0/0 | 6568 | 23 | 4 | 8 | 4 | 1 | 6 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0004 | 0/0 | 6568 | 22 | 0 | 0 | 21 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0005 | 0/0 | 6569 | 2 | 1 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0011 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0018 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0002t0019 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0006t0004 | 0/0 | 6568 | 2 | 0 | 2 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0002c0006t0011 | 0/0 | 6569 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0003c0003t0006 | 0/0 | 6568 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0004c0007t0001 | 0/0 | 6567 | 3 | 3 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0005c0009t0014 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0005c0009t0015 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0006c0010t0001 | 0/0 | 6567 | 2 | 0 | 0 | 0 | 0 | 2 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0007c0012t0005 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0008c0016t0001 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0009c0018t0007 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| a0010c0011t0002 | 1/0 | 6568 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | copy fasta | chr5 | 131636714 | 131802017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0007g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0008g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0009g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0010g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0016g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0017g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0022g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0001t0023g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0005t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0008t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0008t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0013t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0014t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0015t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0001c0017t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0018g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0002t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0006t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0006t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0002c0006t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0003c0003t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0004c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0004c0007t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0004c0007t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0005c0009t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0005c0009t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0006c0010t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0006c0010t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0007c0012t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0008c0016t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0009c0018t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| a0010c0011t0002g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0146 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0325 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0045 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0158 | EUR | IBS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0311 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0126 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01978 | hp1 | a0002 | c0006 | t0011 | g0138 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01981 | hp2 | a0002 | c0006 | t0004 | g0141 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0154 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0283 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0296 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02071 | hp1 | a0009 | c0018 | t0007 | g0017 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02071 | hp2 | a0002 | c0002 | t0018 | g0284 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02258 | hp2 | a0003 | c0003 | t0006 | g0310 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02280 | hp1 | a0003 | c0003 | t0006 | g0315 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02293 | hp1 | a0002 | c0006 | t0004 | g0125 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02572 | hp1 | a0001 | c0005 | t0007 | g0065 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0272 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02615 | hp1 | a0005 | c0009 | t0015 | g0051 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02615 | hp2 | a0001 | c0014 | t0003 | g0026 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0324 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02717 | hp1 | a0001 | c0015 | t0001 | g0326 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02723 | hp1 | a0003 | c0003 | t0006 | g0317 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02738 | hp1 | a0001 | c0001 | t0021 | g0012 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0066 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0064 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02965 | hp2 | a0003 | c0003 | t0006 | g0319 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0072 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02976 | hp1 | a0004 | c0007 | t0001 | g0181 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03041 | hp1 | a0005 | c0009 | t0014 | g0050 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03098 | hp1 | a0004 | c0007 | t0001 | g0174 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03130 | hp1 | a0004 | c0007 | t0001 | g0182 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03130 | hp2 | a0003 | c0003 | t0006 | g0318 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0067 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0307 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03225 | hp1 | a0003 | c0003 | t0006 | g0312 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03453 | hp2 | a0003 | c0003 | t0006 | g0316 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0288 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03688 | hp1 | a0006 | c0010 | t0001 | g0291 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0161 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0297 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0134 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04199 | hp1 | a0001 | c0013 | t0001 | g0171 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG04199 | hp2 | a0002 | c0002 | t0005 | g0124 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18522 | hp2 | a0003 | c0003 | t0006 | g0314 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18939 | hp2 | a0007 | c0012 | t0005 | g0117 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18940 | hp2 | a0001 | c0008 | t0002 | g0285 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0178 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0119 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0137 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0236 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18954 | hp2 | a0002 | c0002 | t0004 | g0136 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18957 | hp2 | a0002 | c0002 | t0004 | g0145 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0127 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18962 | hp2 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18966 | hp2 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18968 | hp1 | a0002 | c0002 | t0004 | g0142 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18970 | hp1 | a0001 | c0001 | t0023 | g0228 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18977 | hp1 | a0008 | c0016 | t0001 | g0190 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18977 | hp2 | a0002 | c0002 | t0011 | g0135 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0299 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18978 | hp2 | a0002 | c0002 | t0004 | g0287 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18980 | hp1 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18980 | hp2 | a0001 | c0001 | t0010 | g0213 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18981 | hp2 | a0002 | c0002 | t0004 | g0052 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18984 | hp2 | a0002 | c0002 | t0004 | g0155 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18991 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18995 | hp1 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18995 | hp2 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19010 | hp2 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19012 | hp1 | a0002 | c0002 | t0004 | g0139 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0043 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0068 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19058 | hp1 | a0001 | c0001 | t0022 | g0205 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19058 | hp2 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19064 | hp2 | a0001 | c0001 | t0017 | g0103 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19065 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19074 | hp2 | a0002 | c0002 | t0004 | g0160 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19076 | hp2 | a0001 | c0001 | t0010 | g0168 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19077 | hp2 | a0001 | c0008 | t0002 | g0110 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19240 | hp1 | a0001 | c0005 | t0007 | g0070 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | ASW | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0323 | AFR | ASW | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | TSI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20905 | hp1 | a0006 | c0010 | t0001 | g0203 | SAS | GIH | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | GIH | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01123 | hp1 | a0001 | c0001 | t0016 | g0320 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0078 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02486 | hp2 | a0002 | c0002 | t0019 | g0058 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02559 | hp1 | a0003 | c0003 | t0006 | g0313 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG02559 | hp2 | a0001 | c0017 | t0001 | g0062 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0231 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0301 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0218 | REF | REF | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| homoSapiens_grch38 | hp1 | a0010 | c0011 | t0002 | g0321 | REF | REF | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131671665
|
C | T | 1 | a0008 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2779G>A | p.Val927Ile | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2875/6568 | 2779/3501 | 927/1166 | chr5 | 131671665 | ||
| chr5:131671794
|
A | G | 1 | a0005 | 2 | HG02615.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2650T>C | p.Phe884Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2746/6568 | 2650/3501 | 884/1166 | chr5 | 131671794 | ||
| chr5:131671914
|
T | C | 1 | a0004 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.2530A>G | p.Ile844Val | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2626/6568 | 2530/3501 | 844/1166 | chr5 | 131671914 | ||
| chr5:131672232
|
C | A | 1 | a0003 | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
missense_variant | MODERATE | c.2212G>T | p.Val738Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2308/6568 | 2212/3501 | 738/1166 | chr5 | 131672232 | ||
| chr5:131672501
|
T | C | 8 | a0001a0003a0004others(5): Show | 274 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(271): Show |
missense_variant | MODERATE | c.1943A>G | p.Gln648Arg | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2039/6568 | 1943/3501 | 648/1166 | chr5 | 131672501 | ||
| chr5:131677804
|
T | C | 1 | a0009 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1418A>G | p.Asn473Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/18 | 1514/6568 | 1418/3501 | 473/1166 | chr5 | 131677804 | ||
| chr5:131704262
|
T | C | 1 | a0006 | 2 | HG03688.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.919A>G | p.Ile307Val | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/18 | 1015/6568 | 919/3501 | 307/1166 | chr5 | 131704262 | ||
| chr5:131730936
|
A | C | 1 | a0007 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.322T>G | p.Ser108Ala | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/18 | 418/6568 | 322/3501 | 108/1166 | chr5 | 131730936 | ||
| chr5:131731032
|
C | A | 9 | a0001a0002a0003others(6): Show | 327 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(324): Show |
missense_variant | MODERATE | c.226G>T | p.Gly76Cys | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/18 | 322/6568 | 226/3501 | 76/1166 | chr5 | 131731032 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131670580
|
C | T | 1 | a0001c0017 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2991G>A | p.Gly997Gly | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/18 | 3087/6568 | 2991/3501 | 997/1166 | chr5 | 131670580 | ||
| chr5:131672017
|
A | G | 1 | a0003c0003 | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.2427T>C | p.Asp809Asp | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2523/6568 | 2427/3501 | 809/1166 | chr5 | 131672017 | ||
| chr5:131672053
|
A | G | 1 | a0001c0008 | 2 | NA18940.hp2 NA19077.hp2 |
synonymous_variant | LOW | c.2391T>C | p.Thr797Thr | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2487/6568 | 2391/3501 | 797/1166 | chr5 | 131672053 | ||
| chr5:131672094
|
A | G | 1 | a0001c0004 | 6 | HG02155.hp2 HG03927.hp1 NA18940.hp1 others(3): Show |
synonymous_variant | LOW | c.2350T>C | p.Leu784Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2446/6568 | 2350/3501 | 784/1166 | chr5 | 131672094 | ||
| chr5:131672791
|
C | T | 1 | a0002c0006 | 3 | HG01978.hp1 HG01981.hp2 HG02293.hp1 |
synonymous_variant | LOW | c.1653G>A | p.Thr551Thr | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 1749/6568 | 1653/3501 | 551/1166 | chr5 | 131672791 | ||
| chr5:131706425
|
C | T | 1 | a0001c0015 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.900G>A | p.Gly300Gly | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/18 | 996/6568 | 900/3501 | 300/1166 | chr5 | 131706425 | ||
| chr5:131710588
|
A | C | 1 | a0001c0014 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.696T>G | p.Ser232Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/18 | 792/6568 | 696/3501 | 232/1166 | chr5 | 131710588 | ||
| chr5:131719057
|
G | A | 1 | a0001c0005 | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.459C>T | p.Ser153Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/18 | 555/6568 | 459/3501 | 153/1166 | chr5 | 131719057 | ||
| chr5:131719385
|
A | G | 1 | a0001c0013 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.387T>C | p.Leu129Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 4/18 | 483/6568 | 387/3501 | 129/1166 | chr5 | 131719385 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131642181
|
C | T | 1 | a0002c0002t0019 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2504G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2504 | chr5 | 131642181 | |||||
| chr5:131642256
|
G | A | 1 | a0001c0001t0016 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2429C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2429 | chr5 | 131642256 | |||||
| chr5:131642310
|
T | G | 4 | a0002c0002t0004a0002c0002t0011a0002c0006t0004others(1): Show | 26 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2375A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2375 | chr5 | 131642310 | |||||
| chr5:131642439
|
C | G | 3 | a0001c0001t0003a0001c0001t0013a0001c0014t0003 | 30 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2246G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2246 | chr5 | 131642439 | |||||
| chr5:131642867
|
C | CA | 7 | a0001c0001t0005a0001c0001t0016a0001c0001t0021others(4): Show | 25 | HG01099.hp1 HG01123.hp1 HG01261.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1817dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1817 | chr5 | 131642867 | |||||
| chr5:131642867
|
CA | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(15): Show | 174 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1817delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1817 | chr5 | 131642867 | |||||
| chr5:131642867
|
CAA | C | 3 | a0001c0001t0010a0002c0002t0019a0005c0009t0014 | 7 | HG02486.hp2 HG03041.hp1 NA18941.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1816_*1817delTT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1816 | chr5 | 131642867 | |||||
| chr5:131642966
|
A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1719T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1719 | chr5 | 131642966 | |||||
| chr5:131643485
|
T | C | 2 | a0005c0009t0014a0005c0009t0015 | 2 | HG02615.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1200A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1200 | chr5 | 131643485 | |||||
| chr5:131643638
|
GA | G | 1 | a0001c0001t0009 | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1046delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1046 | chr5 | 131643638 | |||||
| chr5:131643639
|
A | G | 27 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(24): Show | 199 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1046T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1046 | chr5 | 131643639 | |||||
| chr5:131643674
|
T | C | 1 | a0001c0001t0017 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1011 | chr5 | 131643674 | |||||
| chr5:131643680
|
G | A | 1 | a0002c0002t0018 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1005 | chr5 | 131643680 | |||||
| chr5:131643725
|
T | C | 1 | a0001c0001t0022 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 960 | chr5 | 131643725 | |||||
| chr5:131644223
|
C | T | 4 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(1): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*462G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 462 | chr5 | 131644223 | |||||
| chr5:131644228
|
T | C | 1 | a0002c0002t0019 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 457 | chr5 | 131644228 | |||||
| chr5:131644334
|
G | A | 17 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(14): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 351 | chr5 | 131644334 | |||||
| chr5:131644663
|
T | C | 1 | a0001c0001t0023 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 22 | chr5 | 131644663 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:131644843
|
G | A | 2 | a0002c0002t0004g0052a0002c0002t0004g0134 | 2 | HG03927.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3423-80C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644843 | ||||||
| chr5:131644877
|
G | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3423-114C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644877 | ||||||
| chr5:131644890
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3423-127C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644890 | ||||||
| chr5:131644953
|
G | A | 1 | a0001c0001t0005g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3423-190C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644953 | ||||||
| chr5:131645056
|
G | A | 10 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074others(7): Show | 10 | HG00438.hp1 HG01261.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3423-293C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645056 | ||||||
| chr5:131645309
|
C | CA | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3423-547dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645309 | ||||||
| chr5:131645336
|
A | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3423-573T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645336 | ||||||
| chr5:131645459
|
A | G | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3423-696T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645459 | ||||||
| chr5:131645561
|
C | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3423-798G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645561 | ||||||
| chr5:131645763
|
C | A | 1 | a0002c0002t0002g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3423-1000G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645763 | ||||||
| chr5:131645765
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3423-1002T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645765 | ||||||
| chr5:131645901
|
A | C | 2 | a0002c0002t0004g0142a0002c0002t0004g0283 | 2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3423-1138T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645901 | ||||||
| chr5:131646138
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3422+952A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646138 | ||||||
| chr5:131646242
|
T | C | 2 | a0001c0001t0002g0149a0001c0001t0002g0151 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3422+848A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646242 | ||||||
| chr5:131646425
|
T | C | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3422+665A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646425 | ||||||
| chr5:131646468
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3422+622G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646468 | ||||||
| chr5:131646501
|
A | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.3422+589T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646501 | ||||||
| chr5:131646688
|
T | C | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3422+402A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646688 | ||||||
| chr5:131646720
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3422+370A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646720 | ||||||
| chr5:131646741
|
T | A | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3422+349A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646741 | ||||||
| chr5:131646985
|
T | C | 3 | a0001c0001t0001g0294a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01175.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3422+105A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646985 | ||||||
| chr5:131646987
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3422+103T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646987 | ||||||
| chr5:131647075
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.3422+15T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131647075 | ||||||
| chr5:131647079
|
C | T | 1 | a0006c0010t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3422+11G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131647079 | ||||||
| chr5:131647356
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0008g0301 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3307-151A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647356 | ||||||
| chr5:131647416
|
C | CTT | 193 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 193 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.3307-213_3307-212d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647416 | ||||||
| chr5:131647416
|
C | CTTT | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-214_3307-212d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647416 | ||||||
| chr5:131647559
|
C | T | 4 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0059others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3307-354G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647559 | ||||||
| chr5:131647631
|
C | A | 2 | a0002c0002t0004g0007a0002c0002t0004g0160 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3307-426G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647631 | ||||||
| chr5:131647677
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0289 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3307-472G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647677 | ||||||
| chr5:131647679
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3307-474A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647679 | ||||||
| chr5:131647728
|
A | G | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3307-523T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647728 | ||||||
| chr5:131647796
|
T | C | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3307-591A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647796 | ||||||
| chr5:131648077
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3307-872G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648077 | ||||||
| chr5:131648092
|
G | A | 1 | a0003c0003t0006g0319 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3307-887C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648092 | ||||||
| chr5:131648173
|
T | TA | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(154): Show | 157 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.3307-969dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648173 | ||||||
| chr5:131648173
|
TA | T | 13 | a0001c0001t0002g0086a0001c0001t0002g0099a0001c0001t0002g0104others(10): Show | 13 | HG00639.hp1 HG01081.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.3307-969delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648173 | ||||||
| chr5:131648310
|
C | CA | 7 | a0001c0001t0003g0027a0001c0001t0009g0018a0001c0001t0009g0044others(4): Show | 7 | HG01496.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-1106dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648310 | ||||||
| chr5:131648428
|
G | C | 1 | a0002c0002t0002g0005 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3307-1223C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648428 | ||||||
| chr5:131648470
|
T | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3307-1265A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648470 | ||||||
| chr5:131648602
|
A | T | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3307-1397T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648602 | ||||||
| chr5:131648714
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3307-1509A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648714 | ||||||
| chr5:131648824
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3307-1619G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648824 | ||||||
| chr5:131648894
|
G | A | 2 | a0001c0001t0005g0115a0001c0001t0005g0154 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3307-1689C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648894 | ||||||
| chr5:131649033
|
T | C | 2 | a0002c0002t0002g0158a0002c0002t0002g0159 | 2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3307-1828A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649033 | ||||||
| chr5:131649600
|
G | A | 2 | a0002c0002t0004g0052a0002c0002t0004g0134 | 2 | HG03927.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3306+2202C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649600 | ||||||
| chr5:131649634
|
A | C | 1 | a0001c0001t0002g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3306+2168T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649634 | ||||||
| chr5:131649757
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3306+2045G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649757 | ||||||
| chr5:131649758
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3306+2044A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649758 | ||||||
| chr5:131649833
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3306+1969A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649833 | ||||||
| chr5:131649952
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3306+1850C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649952 | ||||||
| chr5:131650004
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3306+1798T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650004 | ||||||
| chr5:131650013
|
A | G | 2 | a0001c0001t0003g0305a0001c0001t0003g0308 | 2 | HG00639.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3306+1789T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650013 | ||||||
| chr5:131650095
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3306+1707G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650095 | ||||||
| chr5:131650619
|
G | A | 1 | a0001c0013t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3306+1183C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650619 | ||||||
| chr5:131650733
|
T | G | 1 | a0002c0002t0002g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3306+1069A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650733 | ||||||
| chr5:131650859
|
T | C | 1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3306+943A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650859 | ||||||
| chr5:131651056
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3306+746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651056 | ||||||
| chr5:131651086
|
TA | T | 39 | a0001c0001t0001g0219a0001c0001t0001g0302a0001c0001t0003g0019others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3306+715delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651086 | ||||||
| chr5:131651391
|
C | G | 7 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3306+411G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651391 | ||||||
| chr5:131651481
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3306+321C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651481 | ||||||
| chr5:131651538
|
T | G | 1 | a0001c0001t0005g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3306+264A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651538 | ||||||
| chr5:131652307
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-308C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652307 | ||||||
| chr5:131652308
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-309G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652308 | ||||||
| chr5:131652336
|
A | G | 190 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(187): Show | 190 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.3109-337T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652336 | ||||||
| chr5:131652342
|
A | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0227a0001c0001t0001g0233others(1): Show | 4 | HG00609.hp2 NA18957.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-343T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652342 | ||||||
| chr5:131652450
|
G | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-451C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652450 | ||||||
| chr5:131652511
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-512G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652511 | ||||||
| chr5:131652512
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-513C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652512 | ||||||
| chr5:131652563
|
G | A | 13 | a0001c0001t0003g0019a0001c0001t0003g0030a0001c0001t0003g0032others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3109-564C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652563 | ||||||
| chr5:131652620
|
C | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-621G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652620 | ||||||
| chr5:131652696
|
A | T | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-697T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652696 | ||||||
| chr5:131652759
|
T | C | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-760A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652759 | ||||||
| chr5:131652887
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-888G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652887 | ||||||
| chr5:131652965
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-966T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652965 | ||||||
| chr5:131653002
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3109-1003T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653002 | ||||||
| chr5:131653088
|
G | A | 7 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-1089C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653088 | ||||||
| chr5:131653197
|
TCAAAATA others(16): Show |
T | 1 | a0001c0001t0002g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3109-1221_3109-119 others(27): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653197 | ||||||
| chr5:131653207
|
C | G | 1 | a0002c0002t0004g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3109-1208G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653207 | ||||||
| chr5:131653262
|
G | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3109-1263C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653262 | ||||||
| chr5:131653309
|
G | A | 24 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(21): Show | 24 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3109-1310C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653309 | ||||||
| chr5:131653526
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-1527G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653526 | ||||||
| chr5:131653609
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-1610C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653609 | ||||||
| chr5:131653653
|
T | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0151 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3109-1654A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653653 | ||||||
| chr5:131653733
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.3109-1734G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653733 | ||||||
| chr5:131653766
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-1767G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653766 | ||||||
| chr5:131653975
|
C | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-1976G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653975 | ||||||
| chr5:131653976
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-1977C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653976 | ||||||
| chr5:131654381
|
T | C | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3109-2382A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654381 | ||||||
| chr5:131654394
|
C | T | 1 | a0001c0001t0008g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3109-2395G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654394 | ||||||
| chr5:131654601
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-2602C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654601 | ||||||
| chr5:131654651
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-2652A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654651 | ||||||
| chr5:131654691
|
T | C | 148 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 148 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.3109-2692A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654691 | ||||||
| chr5:131654844
|
G | A | 1 | a0002c0002t0002g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3109-2845C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654844 | ||||||
| chr5:131654890
|
G | T | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3109-2891C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654890 | ||||||
| chr5:131654940
|
A | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-2941T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654940 | ||||||
| chr5:131654962
|
C | T | 5 | a0001c0001t0002g0122a0001c0001t0005g0076a0001c0001t0005g0114others(2): Show | 5 | NA18939.hp2 NA18998.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-2963G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654962 | ||||||
| chr5:131654972
|
C | T | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-2973G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654972 | ||||||
| chr5:131655084
|
C | T | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3109-3085G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655084 | ||||||
| chr5:131655202
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0289 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3109-3203A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655202 | ||||||
| chr5:131655277
|
C | T | 5 | a0001c0001t0002g0122a0001c0001t0005g0076a0001c0001t0005g0114others(2): Show | 5 | NA18939.hp2 NA18998.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-3278G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655277 | ||||||
| chr5:131655659
|
G | A | 4 | a0001c0001t0008g0059a0001c0001t0008g0301a0001c0001t0008g0323others(1): Show | 4 | HG02630.hp1 HG03195.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-3660C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655659 | ||||||
| chr5:131655752
|
C | CA | 187 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(184): Show | 187 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.3109-3754dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655752 | ||||||
| chr5:131655784
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-3785C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655784 | ||||||
| chr5:131655937
|
C | CA | 4 | a0001c0001t0001g0212a0001c0001t0001g0295a0001c0001t0001g0300others(1): Show | 4 | HG02738.hp1 HG03704.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-3939dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655937 | ||||||
| chr5:131655940
|
A | C | 3 | a0001c0001t0001g0226a0006c0010t0001g0203a0006c0010t0001g0291 | 3 | HG03239.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3109-3941T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655940 | ||||||
| chr5:131655941
|
A | C | 7 | a0001c0001t0001g0179a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG00408.hp2 HG02040.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3109-3942T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655941 | ||||||
| chr5:131655942
|
C | A | 119 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(116): Show | 119 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.3109-3943G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655942 | ||||||
| chr5:131656295
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-4296C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656295 | ||||||
| chr5:131656336
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3109-4337G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656336 | ||||||
| chr5:131656412
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3109-4413A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656412 | ||||||
| chr5:131656427
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-4428A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656427 | ||||||
| chr5:131656440
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-4441C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656440 | ||||||
| chr5:131656562
|
T | G | 4 | a0001c0001t0008g0059a0001c0001t0008g0301a0001c0001t0008g0323others(1): Show | 4 | HG02630.hp1 HG03195.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-4563A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656562 | ||||||
| chr5:131656566
|
G | A | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3109-4567C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656566 | ||||||
| chr5:131656591
|
T | G | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(202): Show | 205 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.3109-4592A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656591 | ||||||
| chr5:131656600
|
A | G | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-4601T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656600 | ||||||
| chr5:131656603
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3109-4604T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656603 | ||||||
| chr5:131656644
|
GCTTTTGC others(24): Show |
G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-4676_3109-464 others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656644 | ||||||
| chr5:131656739
|
T | C | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(202): Show | 205 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.3109-4740A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656739 | ||||||
| chr5:131656883
|
T | C | 1 | a0001c0004t0001g0257 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3109-4884A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656883 | ||||||
| chr5:131657019
|
C | CT | 57 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0170others(54): Show | 57 | HG00544.hp1 HG00639.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.3109-5021dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657019 | ||||||
| chr5:131657019
|
CT | C | 111 | a0001c0001t0001g0256a0001c0001t0002g0002a0001c0001t0002g0004others(108): Show | 113 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3109-5021delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657019 | ||||||
| chr5:131657056
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3109-5057G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657056 | ||||||
| chr5:131657250
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-5251G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657250 | ||||||
| chr5:131657369
|
A | T | 2 | a0001c0001t0003g0027a0001c0014t0003g0026 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3109-5370T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657369 | ||||||
| chr5:131657431
|
A | G | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(202): Show | 205 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.3109-5432T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657431 | ||||||
| chr5:131657736
|
C | CA | 35 | a0001c0001t0001g0071a0001c0001t0001g0169a0001c0001t0002g0002others(32): Show | 36 | HG01081.hp1 HG01175.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.3109-5738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657736
|
C | CAA | 66 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0057others(63): Show | 66 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.3109-5739_3109-573 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657736
|
C | CAAA | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 77 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.3109-5740_3109-573 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657736
|
C | CAAAA | 30 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0183others(27): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.3109-5741_3109-573 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657736
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3109-5747_3109-573 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657736
|
CAAAAAA | C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-5743_3109-573 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | ||||||
| chr5:131657783
|
CGGATCTT others(8): Show |
C | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3109-5799_3109-578 others(19): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657783 | ||||||
| chr5:131658040
|
C | CA | 21 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0191others(18): Show | 21 | HG01081.hp1 HG01981.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3109-6042dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | ||||||
| chr5:131658040
|
C | CAA | 6 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(3): Show | 6 | HG01496.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-6043_3109-604 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | ||||||
| chr5:131658040
|
CA | C | 8 | a0001c0001t0001g0175a0001c0001t0002g0106a0001c0001t0003g0025others(5): Show | 8 | HG00639.hp1 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-6042delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | ||||||
| chr5:131658122
|
C | G | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3109-6123G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658122 | ||||||
| chr5:131658217
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-6218T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658217 | ||||||
| chr5:131658423
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3109-6424G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658423 | ||||||
| chr5:131658634
|
G | T | 6 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-6635C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658634 | ||||||
| chr5:131658716
|
G | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-6717C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658716 | ||||||
| chr5:131658736
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.3109-6737C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658736 | ||||||
| chr5:131658785
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-6786A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658785 | ||||||
| chr5:131658907
|
C | CA | 23 | a0001c0001t0002g0083a0001c0001t0002g0094a0001c0001t0002g0099others(20): Show | 23 | HG00544.hp2 HG02040.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3109-6909dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAA | 20 | a0001c0001t0001g0198a0001c0001t0002g0097a0001c0001t0002g0121others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.3109-6910_3109-690 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAA | 18 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0025others(15): Show | 18 | HG00639.hp1 HG00642.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.3109-6911_3109-690 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAA | 61 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0163others(58): Show | 61 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.3109-6912_3109-690 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAAA | 55 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0055others(52): Show | 55 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.3109-6913_3109-690 others(9): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAAAA | 9 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0219others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3109-6914_3109-690 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0177a0001c0001t0008g0022a0001c0001t0008g0023 | 3 | HG02109.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-6919_3109-690 others(15): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0008g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3109-6920_3109-690 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3109-6922_3109-690 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.3109-6917_3109-690 others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131658907
|
CAAAAAAA others(3): Show |
C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-6918_3109-690 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | ||||||
| chr5:131659170
|
G | A | 17 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(14): Show | 17 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3109-7171C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659170 | ||||||
| chr5:131659172
|
T | C | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-7173A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659172 | ||||||
| chr5:131659191
|
A | G | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3109-7192T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659191 | ||||||
| chr5:131659600
|
C | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-7601G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659600 | ||||||
| chr5:131659619
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3109-7620G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659619 | ||||||
| chr5:131659633
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3109-7634C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659633 | ||||||
| chr5:131659649
|
C | T | 4 | a0001c0001t0003g0037a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | HG00642.hp1 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-7650G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659649 | ||||||
| chr5:131659688
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3109-7689A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659688 | ||||||
| chr5:131659780
|
T | C | 1 | a0001c0001t0005g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3109-7781A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659780 | ||||||
| chr5:131660451
|
C | G | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-8452G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660451 | ||||||
| chr5:131660467
|
A | G | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3109-8468T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660467 | ||||||
| chr5:131660511
|
T | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-8512A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660511 | ||||||
| chr5:131660598
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0225 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3109-8599G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660598 | ||||||
| chr5:131660755
|
C | T | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-8756G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660755 | ||||||
| chr5:131660758
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3109-8759T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660758 | ||||||
| chr5:131660809
|
G | A | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3109-8810C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660809 | ||||||
| chr5:131660814
|
T | C | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-8815A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660814 | ||||||
| chr5:131660854
|
G | A | 1 | a0001c0001t0022g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3109-8855C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660854 | ||||||
| chr5:131660869
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0020g0231 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3109-8870C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660869 | ||||||
| chr5:131660939
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-8940C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660939 | ||||||
| chr5:131661062
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3109-9063T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661062 | ||||||
| chr5:131661217
|
GTT | G | 3 | a0001c0001t0001g0163a0001c0001t0002g0098a0001c0001t0008g0059 | 3 | HG03195.hp1 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661217 | ||||||
| chr5:131661218
|
T | TTG | 107 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(104): Show | 107 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTG | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(24): Show | 27 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTG | 6 | a0001c0001t0001g0167a0001c0001t0001g0201a0001c0001t0001g0302others(3): Show | 6 | HG00741.hp2 HG01516.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(1): Show |
20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(3): Show |
16 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0021others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0003g0020a0001c0001t0003g0048a0001c0015t0001g0326 | 3 | HG00642.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0003g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0013g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(22): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(24): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(21): Show |
1 | a0005c0009t0015g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(32): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661218
|
T | TTGTGTGT others(23): Show |
1 | a0005c0009t0014g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | ||||||
| chr5:131661220
|
T | G | 201 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(198): Show | 201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.3109-9221A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | ||||||
| chr5:131661220
|
T | TTG | 13 | a0001c0001t0002g0002a0001c0001t0002g0081a0001c0001t0002g0096others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3109-9223_3109-922 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | ||||||
| chr5:131661220
|
T | TTGTG | 3 | a0002c0002t0002g0079a0002c0002t0002g0159a0002c0002t0005g0126 | 3 | HG01255.hp1 HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3109-9225_3109-922 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | ||||||
| chr5:131661472
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.3108+8991C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661472 | ||||||
| chr5:131661525
|
G | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3108+8938C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661525 | ||||||
| chr5:131661712
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0289 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3108+8751G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661712 | ||||||
| chr5:131661764
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3108+8699G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661764 | ||||||
| chr5:131661768
|
C | T | 1 | a0001c0001t0007g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3108+8695G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661768 | ||||||
| chr5:131661982
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0264 | 2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3108+8481G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661982 | ||||||
| chr5:131662060
|
G | C | 10 | a0001c0001t0001g0063a0001c0001t0008g0022a0001c0001t0008g0023others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+8403C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662060 | ||||||
| chr5:131662309
|
G | GA | 12 | a0001c0001t0001g0183a0001c0001t0002g0004a0001c0001t0002g0053others(9): Show | 12 | HG02135.hp2 HG02155.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.3108+8153dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662309 | ||||||
| chr5:131662453
|
C | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+8010G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662453 | ||||||
| chr5:131662550
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0157 | 2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3108+7913T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662550 | ||||||
| chr5:131662574
|
G | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3108+7889C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662574 | ||||||
| chr5:131662733
|
A | AT | 42 | a0001c0001t0001g0063a0001c0001t0002g0081a0001c0001t0002g0093others(39): Show | 42 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.3108+7729dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | ||||||
| chr5:131662733
|
AT | A | 31 | a0001c0001t0001g0073a0001c0001t0001g0163a0001c0001t0001g0176others(28): Show | 31 | HG00408.hp2 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.3108+7729delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | ||||||
| chr5:131662733
|
ATT | A | 128 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(125): Show | 128 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.3108+7728_3108+772 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | ||||||
| chr5:131662742
|
T | A | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3108+7721A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662742 | ||||||
| chr5:131662931
|
C | T | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3108+7532G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662931 | ||||||
| chr5:131662932
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3108+7531C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662932 | ||||||
| chr5:131663145
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3108+7318A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663145 | ||||||
| chr5:131663198
|
A | G | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3108+7265T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663198 | ||||||
| chr5:131663270
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+7193A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663270 | ||||||
| chr5:131663389
|
A | G | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.3108+7074T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663389 | ||||||
| chr5:131663444
|
C | T | 14 | a0001c0001t0003g0019a0001c0001t0003g0030a0001c0001t0003g0032others(11): Show | 14 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3108+7019G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663444 | ||||||
| chr5:131663526
|
AAAG | A | 24 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(21): Show | 24 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3108+6934_3108+693 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663526 | ||||||
| chr5:131663569
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+6894A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663569 | ||||||
| chr5:131663684
|
T | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+6779A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663684 | ||||||
| chr5:131663714
|
G | C | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+6749C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663714 | ||||||
| chr5:131663879
|
G | C | 1 | a0001c0001t0010g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3108+6584C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663879 | ||||||
| chr5:131664561
|
G | C | 1 | a0002c0002t0004g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3108+5902C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664561 | ||||||
| chr5:131664589
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+5874G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664589 | ||||||
| chr5:131664634
|
C | CA | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0063others(44): Show | 47 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.3108+5828dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | ||||||
| chr5:131664634
|
C | CAA | 124 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(121): Show | 124 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.3108+5827_3108+582 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | ||||||
| chr5:131664634
|
C | CAAA | 28 | a0001c0001t0001g0057a0001c0001t0001g0180a0001c0001t0001g0186others(25): Show | 28 | HG00438.hp2 HG01256.hp1 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.3108+5826_3108+582 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | ||||||
| chr5:131664826
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0008g0022a0001c0001t0008g0023others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+5637A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664826 | ||||||
| chr5:131664888
|
A | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3108+5575T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664888 | ||||||
| chr5:131664955
|
GAT | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+5506_3108+550 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664955 | ||||||
| chr5:131664961
|
C | A | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3108+5502G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664961 | ||||||
| chr5:131664987
|
G | A | 1 | a0001c0001t0002g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3108+5476C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664987 | ||||||
| chr5:131665003
|
A | G | 127 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(124): Show | 127 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.3108+5460T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665003 | ||||||
| chr5:131665018
|
A | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3108+5445T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665018 | ||||||
| chr5:131665131
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3108+5332C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665131 | ||||||
| chr5:131665179
|
A | T | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3108+5284T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665179 | ||||||
| chr5:131665317
|
T | C | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3108+5146A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665317 | ||||||
| chr5:131665449
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3108+5014C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665449 | ||||||
| chr5:131665511
|
T | C | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3108+4952A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665511 | ||||||
| chr5:131665585
|
T | G | 2 | a0001c0001t0003g0035a0001c0001t0008g0301 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3108+4878A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665585 | ||||||
| chr5:131665594
|
G | GT | 9 | a0001c0001t0001g0008a0001c0001t0001g0073a0001c0001t0001g0258others(6): Show | 9 | HG02615.hp1 HG03041.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+4868dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665594 | ||||||
| chr5:131665682
|
C | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3108+4781G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665682 | ||||||
| chr5:131665683
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3108+4780T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665683 | ||||||
| chr5:131665692
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3108+4771G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665692 | ||||||
| chr5:131665695
|
T | C | 7 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3108+4768A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665695 | ||||||
| chr5:131665714
|
C | T | 2 | a0001c0001t0001g0200a0002c0002t0002g0282 | 2 | HG01433.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3108+4749G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665714 | ||||||
| chr5:131665898
|
A | AT | 41 | a0001c0001t0001g0010a0001c0001t0001g0163a0001c0001t0001g0180others(38): Show | 41 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3108+4564_3108+456 others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | ||||||
| chr5:131665898
|
AC | A | 55 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0169others(52): Show | 55 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.3108+4564delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | ||||||
| chr5:131665898
|
ACT | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3108+4563_3108+456 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | ||||||
| chr5:131665899
|
C | CT | 7 | a0001c0001t0002g0085a0001c0001t0002g0122a0001c0001t0005g0286others(4): Show | 7 | HG02273.hp2 HG03927.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.3108+4563dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665899 | ||||||
| chr5:131665899
|
C | T | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.3108+4564G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665899 | ||||||
| chr5:131665941
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.3108+4522C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665941 | ||||||
| chr5:131665963
|
G | A | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+4500C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665963 | ||||||
| chr5:131666057
|
T | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3108+4406A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666057 | ||||||
| chr5:131666138
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+4325G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666138 | ||||||
| chr5:131666139
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3108+4324C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666139 | ||||||
| chr5:131666218
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3108+4245A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666218 | ||||||
| chr5:131666504
|
A | G | 1 | a0001c0001t0002g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3108+3959T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666504 | ||||||
| chr5:131666818
|
A | C | 3 | a0001c0001t0001g0063a0001c0015t0001g0326a0001c0017t0001g0062 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3108+3645T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666818 | ||||||
| chr5:131666834
|
G | A | 1 | a0003c0003t0006g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3108+3629C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666834 | ||||||
| chr5:131666850
|
G | A | 1 | a0001c0001t0010g0013 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3108+3613C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666850 | ||||||
| chr5:131666905
|
C | T | 6 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0059others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+3558G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666905 | ||||||
| chr5:131667099
|
A | G | 304 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(301): Show | 306 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(303): Show |
intron_variant | MODIFIER | c.3108+3364T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667099 | ||||||
| chr5:131667294
|
A | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3108+3169T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667294 | ||||||
| chr5:131667336
|
G | C | 1 | a0001c0005t0001g0072 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3108+3127C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667336 | ||||||
| chr5:131667510
|
G | A | 1 | a0001c0013t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3108+2953C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667510 | ||||||
| chr5:131667573
|
T | G | 1 | a0001c0001t0003g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3108+2890A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | ||||||
| chr5:131667573
|
TTTTG | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3108+2886_3108+288 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | ||||||
| chr5:131667573
|
TTTTGTTT others(5): Show |
T | 4 | a0002c0002t0004g0129a0002c0002t0004g0130a0002c0002t0004g0131others(1): Show | 4 | NA18966.hp2 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+2878_3108+288 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | ||||||
| chr5:131667649
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+2814G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667649 | ||||||
| chr5:131667672
|
T | TCTA | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+2788_3108+279 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667672 | ||||||
| chr5:131667747
|
C | A | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3108+2716G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667747 | ||||||
| chr5:131668118
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3108+2345G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668118 | ||||||
| chr5:131668195
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+2268T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668195 | ||||||
| chr5:131668292
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3108+2171A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668292 | ||||||
| chr5:131668345
|
T | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3108+2118A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668345 | ||||||
| chr5:131668434
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3108+2029G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668434 | ||||||
| chr5:131668465
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3108+1998G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668465 | ||||||
| chr5:131668556
|
G | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3108+1907C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668556 | ||||||
| chr5:131668602
|
T | C | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+1861A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668602 | ||||||
| chr5:131668608
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3108+1855G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668608 | ||||||
| chr5:131668820
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3108+1643C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668820 | ||||||
| chr5:131668883
|
T | G | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3108+1580A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668883 | ||||||
| chr5:131668953
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.3108+1510C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668953 | ||||||
| chr5:131669241
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0153 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.3108+1222C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669241 | ||||||
| chr5:131669268
|
C | A | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+1195G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669268 | ||||||
| chr5:131669273
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+1190C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669273 | ||||||
| chr5:131669488
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3108+975T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669488 | ||||||
| chr5:131669580
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3108+883G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669580 | ||||||
| chr5:131669581
|
G | A | 4 | a0002c0002t0004g0129a0002c0002t0004g0130a0002c0002t0004g0131others(1): Show | 4 | NA18966.hp2 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+882C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669581 | ||||||
| chr5:131669590
|
A | G | 1 | a0002c0002t0002g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3108+873T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669590 | ||||||
| chr5:131669618
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+845A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669618 | ||||||
| chr5:131669645
|
T | A | 1 | a0001c0001t0003g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3108+818A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669645 | ||||||
| chr5:131669666
|
C | A | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+797G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669666 | ||||||
| chr5:131669680
|
A | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0222others(2): Show | 5 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3108+783T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669680 | ||||||
| chr5:131669827
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+636A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669827 | ||||||
| chr5:131669830
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+633G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669830 | ||||||
| chr5:131669907
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3108+556A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669907 | ||||||
| chr5:131669917
|
C | CA | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.3108+545dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669917 | ||||||
| chr5:131669945
|
C | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3108+518G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669945 | ||||||
| chr5:131669990
|
C | A | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+473G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669990 | ||||||
| chr5:131669991
|
T | C | 2 | a0002c0002t0004g0007a0002c0002t0004g0160 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3108+472A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669991 | ||||||
| chr5:131670389
|
A | G | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.3108+74T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131670389 | ||||||
| chr5:131670651
|
A | C | 1 | a0001c0001t0005g0111 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2940-20T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670651 | ||||||
| chr5:131670663
|
T | A | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.2940-32A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670663 | ||||||
| chr5:131670688
|
T | TA | 10 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0183others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940-58dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670688 | ||||||
| chr5:131670703
|
G | C | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2940-72C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670703 | ||||||
| chr5:131670854
|
C | G | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2940-223G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670854 | ||||||
| chr5:131670872
|
A | T | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2940-241T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670872 | ||||||
| chr5:131670919
|
A | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2940-288T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670919 | ||||||
| chr5:131670938
|
A | G | 2 | a0002c0002t0004g0119a0002c0002t0004g0143 | 2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2940-307T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670938 | ||||||
| chr5:131673051
|
G | GT | 17 | a0001c0001t0001g0198a0001c0001t0001g0209a0001c0001t0001g0245others(14): Show | 17 | HG00738.hp2 HG01884.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1520-128dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673051 | ||||||
| chr5:131673051
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1520-127C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673051 | ||||||
| chr5:131673058
|
T | G | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1520-134A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673058 | ||||||
| chr5:131673192
|
C | T | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1520-268G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673192 | ||||||
| chr5:131673657
|
G | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1520-733C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673657 | ||||||
| chr5:131673689
|
A | G | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1520-765T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673689 | ||||||
| chr5:131673708
|
G | A | 1 | a0001c0001t0008g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520-784C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673708 | ||||||
| chr5:131673773
|
C | T | 1 | a0001c0001t0005g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1520-849G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673773 | ||||||
| chr5:131673886
|
A | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520-962T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673886 | ||||||
| chr5:131673972
|
G | A | 6 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520-1048C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673972 | ||||||
| chr5:131673985
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1520-1061C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673985 | ||||||
| chr5:131674220
|
A | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1520-1296T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674220 | ||||||
| chr5:131674535
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1520-1611G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674535 | ||||||
| chr5:131674562
|
C | T | 2 | a0002c0002t0004g0142a0002c0002t0004g0283 | 2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1520-1638G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674562 | ||||||
| chr5:131674791
|
A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0053a0001c0001t0002g0104others(2): Show | 5 | NA18941.hp1 NA18946.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520-1867T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674791 | ||||||
| chr5:131674818
|
C | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0163a0001c0001t0001g0180others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01978.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520-1894G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674818 | ||||||
| chr5:131674819
|
TTTACAAA others(2): Show |
T | 35 | a0001c0001t0001g0010a0001c0001t0001g0163a0001c0001t0001g0180others(32): Show | 35 | HG00544.hp1 HG00609.hp2 HG01978.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520-1904_1520-189 others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674819 | ||||||
| chr5:131674953
|
A | G | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1520-2029T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674953 | ||||||
| chr5:131675292
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1520-2368G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675292 | ||||||
| chr5:131675642
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1519+2061T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675642 | ||||||
| chr5:131675688
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1519+2015C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675688 | ||||||
| chr5:131675890
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1519+1813G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675890 | ||||||
| chr5:131676198
|
G | A | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1519+1505C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676198 | ||||||
| chr5:131676212
|
C | T | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1519+1491G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676212 | ||||||
| chr5:131676305
|
A | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1519+1398T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676305 | ||||||
| chr5:131676311
|
C | A | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1519+1392G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676311 | ||||||
| chr5:131676314
|
T | C | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1519+1389A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676314 | ||||||
| chr5:131676330
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1519+1373C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676330 | ||||||
| chr5:131676476
|
G | C | 7 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519+1227C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676476 | ||||||
| chr5:131676538
|
G | A | 4 | a0001c0001t0001g0302a0004c0007t0001g0174a0004c0007t0001g0181others(1): Show | 4 | HG02976.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519+1165C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676538 | ||||||
| chr5:131676565
|
C | T | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1519+1138G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676565 | ||||||
| chr5:131676678
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1519+1025C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676678 | ||||||
| chr5:131676726
|
C | G | 1 | a0001c0001t0003g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1519+977G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676726 | ||||||
| chr5:131677170
|
C | T | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1519+533G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677170 | ||||||
| chr5:131677341
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1519+362A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677341 | ||||||
| chr5:131677597
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1519+106A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677597 | ||||||
| chr5:131677914
|
A | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1350-42T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131677914 | ||||||
| chr5:131677924
|
A | AG | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1350-53dupC | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131677924 | ||||||
| chr5:131678057
|
G | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1350-185C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678057 | ||||||
| chr5:131678122
|
G | A | 143 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1350-250C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678122 | ||||||
| chr5:131678626
|
T | TG | 325 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 327 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(324): Show |
intron_variant | MODIFIER | c.1349+402dupC | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678626 | ||||||
| chr5:131678690
|
A | G | 304 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(301): Show | 306 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(303): Show |
intron_variant | MODIFIER | c.1349+339T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678690 | ||||||
| chr5:131678722
|
T | C | 1 | a0001c0001t0003g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1349+307A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678722 | ||||||
| chr5:131679002
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1349+27T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131679002 | ||||||
| chr5:131679214
|
A | T | 1 | a0001c0001t0007g0240 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1203-39T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679214 | ||||||
| chr5:131679296
|
A | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-121T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679296 | ||||||
| chr5:131679297
|
A | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-122T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679297 | ||||||
| chr5:131679482
|
A | G | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1203-307T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679482 | ||||||
| chr5:131679510
|
G | A | 5 | a0001c0001t0008g0059a0001c0001t0008g0301a0001c0001t0008g0323others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203-335C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679510 | ||||||
| chr5:131679631
|
T | C | 3 | a0001c0005t0001g0072a0001c0005t0007g0065a0001c0005t0007g0070 | 3 | HG02572.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1203-456A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679631 | ||||||
| chr5:131679653
|
A | G | 130 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1203-478T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679653 | ||||||
| chr5:131679870
|
A | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1203-695T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679870 | ||||||
| chr5:131679921
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0005g0080 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1203-746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679921 | ||||||
| chr5:131680082
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1203-907A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680082 | ||||||
| chr5:131680246
|
A | G | 4 | a0002c0002t0002g0079a0002c0002t0002g0140a0002c0002t0002g0288others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-1071T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680246 | ||||||
| chr5:131680486
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-1311A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680486 | ||||||
| chr5:131681019
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0264 | 2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1203-1844G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681019 | ||||||
| chr5:131681245
|
C | T | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1203-2070G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681245 | ||||||
| chr5:131681663
|
G | GA | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1203-2489dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681663 | ||||||
| chr5:131681762
|
T | TA | 95 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 95 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1203-2588dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | ||||||
| chr5:131681762
|
T | TAA | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1203-2589_1203-258 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | ||||||
| chr5:131681762
|
T | TAAA | 15 | a0001c0001t0001g0163a0001c0001t0001g0208a0001c0001t0001g0225others(12): Show | 15 | HG01081.hp1 HG01978.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203-2590_1203-258 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | ||||||
| chr5:131681796
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1203-2621T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681796 | ||||||
| chr5:131682138
|
TATAA | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-2967_1203-296 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682138 | ||||||
| chr5:131682211
|
A | C | 12 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 12 | HG01081.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1203-3036T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682211 | ||||||
| chr5:131682233
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1203-3058T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682233 | ||||||
| chr5:131682258
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1203-3083A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682258 | ||||||
| chr5:131682321
|
T | C | 4 | a0002c0002t0002g0123a0002c0002t0002g0161a0002c0002t0002g0272others(1): Show | 4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-3146A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682321 | ||||||
| chr5:131682522
|
C | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0260a0001c0001t0001g0262 | 3 | HG02165.hp2 HG04184.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1203-3347G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682522 | ||||||
| chr5:131682548
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1203-3373C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682548 | ||||||
| chr5:131682711
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1203-3536G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682711 | ||||||
| chr5:131682716
|
C | CA | 15 | a0001c0001t0001g0183a0001c0001t0003g0042a0001c0001t0007g0240others(12): Show | 15 | HG01884.hp1 HG02056.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203-3542dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682716 | ||||||
| chr5:131682876
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203-3701G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682876 | ||||||
| chr5:131682954
|
TA | T | 15 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(12): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203-3780delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682954 | ||||||
| chr5:131682996
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1203-3821G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682996 | ||||||
| chr5:131683085
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1203-3910T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683085 | ||||||
| chr5:131683414
|
G | A | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1203-4239C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683414 | ||||||
| chr5:131683504
|
A | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1203-4329T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683504 | ||||||
| chr5:131683552
|
C | CA | 48 | a0001c0001t0001g0063a0001c0001t0001g0163a0001c0001t0001g0191others(45): Show | 48 | HG00544.hp2 HG01070.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1203-4378dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | ||||||
| chr5:131683552
|
C | CAA | 6 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0073others(3): Show | 6 | HG02280.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-4379_1203-437 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | ||||||
| chr5:131683552
|
CA | C | 11 | a0001c0001t0008g0301a0001c0015t0001g0326a0003c0003t0006g0310others(8): Show | 11 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1203-4378delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | ||||||
| chr5:131683633
|
A | G | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1203-4458T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683633 | ||||||
| chr5:131683668
|
G | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-4493C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683668 | ||||||
| chr5:131683809
|
A | G | 6 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-4634T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683809 | ||||||
| chr5:131684126
|
C | A | 1 | a0001c0001t0003g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203-4951G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684126 | ||||||
| chr5:131684150
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1203-4975T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684150 | ||||||
| chr5:131684151
|
T | C | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1203-4976A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684151 | ||||||
| chr5:131684178
|
A | G | 2 | a0002c0002t0002g0003a0002c0002t0002g0005 | 2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1203-5003T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684178 | ||||||
| chr5:131684218
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1203-5043C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684218 | ||||||
| chr5:131684396
|
A | C | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1203-5221T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684396 | ||||||
| chr5:131684402
|
A | G | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0053others(45): Show | 49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-5227T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684402 | ||||||
| chr5:131684409
|
A | G | 19 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0002g0152others(16): Show | 19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1203-5234T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684409 | ||||||
| chr5:131684575
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1203-5400G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684575 | ||||||
| chr5:131684589
|
C | A | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1203-5414G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684589 | ||||||
| chr5:131684643
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1203-5468C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684643 | ||||||
| chr5:131684653
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1203-5478A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684653 | ||||||
| chr5:131685120
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-5945G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685120 | ||||||
| chr5:131685360
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1203-6185T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685360 | ||||||
| chr5:131685448
|
C | CT | 199 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(196): Show | 200 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(197): Show |
intron_variant | MODIFIER | c.1203-6274dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685448 | ||||||
| chr5:131685563
|
T | C | 1 | a0001c0001t0003g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1203-6388A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685563 | ||||||
| chr5:131685672
|
T | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1203-6497A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685672 | ||||||
| chr5:131685803
|
T | TA | 260 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(257): Show | 261 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(258): Show |
intron_variant | MODIFIER | c.1203-6629dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685803 | ||||||
| chr5:131685803
|
T | TAA | 12 | a0001c0001t0002g0149a0001c0001t0002g0151a0003c0003t0006g0310others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1203-6630_1203-662 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685803 | ||||||
| chr5:131685940
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1203-6765A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685940 | ||||||
| chr5:131686358
|
T | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0053a0001c0001t0002g0075others(8): Show | 11 | HG02135.hp2 HG02155.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1203-7183A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686358 | ||||||
| chr5:131686492
|
G | A | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203-7317C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686492 | ||||||
| chr5:131686897
|
A | G | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203-7722T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686897 | ||||||
| chr5:131686923
|
C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0188a0001c0001t0001g0215others(1): Show | 4 | HG00733.hp1 HG01070.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-7748G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686923 | ||||||
| chr5:131686938
|
C | A | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1203-7763G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686938 | ||||||
| chr5:131687056
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0008g0301 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1203-7881A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687056 | ||||||
| chr5:131687348
|
C | T | 1 | a0002c0002t0004g0129 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1203-8173G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687348 | ||||||
| chr5:131687465
|
C | T | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0053others(45): Show | 49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-8290G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687465 | ||||||
| chr5:131687615
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1203-8440G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687615 | ||||||
| chr5:131687806
|
G | C | 2 | a0001c0001t0003g0027a0001c0014t0003g0026 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1203-8631C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687806 | ||||||
| chr5:131688101
|
T | TA | 48 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0053others(45): Show | 49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-8927dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688101 | ||||||
| chr5:131688101
|
TA | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203-8927delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688101 | ||||||
| chr5:131688289
|
T | TA | 43 | a0001c0001t0001g0191a0001c0001t0001g0217a0001c0001t0003g0019others(40): Show | 43 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1203-9115dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688289 | ||||||
| chr5:131688289
|
TA | T | 13 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0073others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1203-9115delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688289 | ||||||
| chr5:131688375
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-9200G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688375 | ||||||
| chr5:131688662
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1203-9487A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688662 | ||||||
| chr5:131688702
|
T | TA | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1203-9528dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688702 | ||||||
| chr5:131688937
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1203-9762G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688937 | ||||||
| chr5:131689081
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1202+9836C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689081 | ||||||
| chr5:131689152
|
C | CA | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1202+9764dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689152 | ||||||
| chr5:131689778
|
A | G | 321 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(318): Show | 323 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(320): Show |
intron_variant | MODIFIER | c.1202+9139T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689778 | ||||||
| chr5:131689849
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1202+9068T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689849 | ||||||
| chr5:131690011
|
G | A | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1202+8906C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690011 | ||||||
| chr5:131690080
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+8837C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690080 | ||||||
| chr5:131690119
|
A | T | 2 | a0002c0002t0004g0007a0002c0002t0004g0160 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1202+8798T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690119 | ||||||
| chr5:131690127
|
G | T | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1202+8790C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690127 | ||||||
| chr5:131690131
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+8786C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690131 | ||||||
| chr5:131690146
|
C | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1202+8771G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690146 | ||||||
| chr5:131690397
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1202+8520A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690397 | ||||||
| chr5:131690483
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1202+8434T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690483 | ||||||
| chr5:131690525
|
G | A | 17 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0185others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1202+8392C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690525 | ||||||
| chr5:131690598
|
G | A | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+8319C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690598 | ||||||
| chr5:131690625
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0224 | 2 | HG01993.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1202+8292G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690625 | ||||||
| chr5:131690697
|
G | A | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1202+8220C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690697 | ||||||
| chr5:131690897
|
C | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1202+8020G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690897 | ||||||
| chr5:131690933
|
A | G | 1 | a0001c0001t0008g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1202+7984T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690933 | ||||||
| chr5:131691154
|
G | A | 1 | a0001c0001t0001g0218 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1202+7763C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691154 | ||||||
| chr5:131691293
|
G | C | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1202+7624C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691293 | ||||||
| chr5:131691469
|
A | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+7448T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691469 | ||||||
| chr5:131691498
|
A | T | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1202+7419T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691498 | ||||||
| chr5:131691541
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1202+7376C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691541 | ||||||
| chr5:131691786
|
G | A | 1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1202+7131C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691786 | ||||||
| chr5:131691994
|
A | G | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1202+6923T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691994 | ||||||
| chr5:131692040
|
A | G | 7 | a0001c0001t0002g0094a0001c0001t0002g0098a0001c0001t0002g0101others(4): Show | 7 | NA18940.hp2 NA18953.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+6877T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692040 | ||||||
| chr5:131692149
|
A | C | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1202+6768T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692149 | ||||||
| chr5:131692156
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+6761C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692156 | ||||||
| chr5:131692188
|
T | C | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202+6729A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692188 | ||||||
| chr5:131692311
|
C | T | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1202+6606G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692311 | ||||||
| chr5:131692324
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1202+6593T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692324 | ||||||
| chr5:131692333
|
G | A | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1202+6584C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692333 | ||||||
| chr5:131692465
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+6452T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692465 | ||||||
| chr5:131692503
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1202+6414T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692503 | ||||||
| chr5:131692787
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1202+6130G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692787 | ||||||
| chr5:131693021
|
T | A | 7 | a0001c0001t0001g0322a0001c0001t0005g0077a0001c0001t0005g0113others(4): Show | 7 | HG01261.hp1 HG02486.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5896A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693021 | ||||||
| chr5:131693230
|
T | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1202+5687A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693230 | ||||||
| chr5:131693260
|
TA | T | 11 | a0001c0001t0001g0177a0001c0001t0001g0184a0001c0001t0003g0303others(8): Show | 11 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1202+5656delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693260 | ||||||
| chr5:131693277
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+5640A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693277 | ||||||
| chr5:131693289
|
AATATATA others(29): Show |
A | 2 | a0001c0004t0001g0232a0001c0004t0001g0257 | 2 | HG02155.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1202+5592_1202+562 others(40): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693289 | ||||||
| chr5:131693297
|
C | CAT | 3 | a0001c0001t0002g0086a0002c0002t0002g0005a0002c0002t0002g0140 | 3 | HG00438.hp1 HG03209.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1202+5618_1202+561 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | ||||||
| chr5:131693297
|
C | CATATATA others(35): Show |
1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1202+5619_1202+562 others(46): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | ||||||
| chr5:131693297
|
CATAT | C | 8 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0223others(5): Show | 8 | HG01516.hp1 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202+5616_1202+561 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | ||||||
| chr5:131693301
|
T | TATATATA others(19): Show |
2 | a0001c0001t0001g0262a0001c0001t0007g0229 | 2 | NA18962.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1202+5615_1202+561 others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693301 | ||||||
| chr5:131693303
|
T | TATATATA others(1): Show |
10 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0006g0054others(7): Show | 10 | HG01081.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693303
|
T | TATATATA others(15): Show |
1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(26): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693303
|
T | TATATATA others(3): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0221others(1): Show | 4 | HG00408.hp2 HG01433.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693303
|
T | TATATATA others(17): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0238 | 2 | HG00438.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(28): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693303
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693303
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(23): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | ||||||
| chr5:131693305
|
T | TATATATA others(1): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+5611_1202+561 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693305 | ||||||
| chr5:131693307
|
T | TATATAC | 4 | a0001c0001t0001g0235a0001c0001t0001g0294a0001c0001t0003g0032others(1): Show | 4 | HG01175.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+5609_1202+561 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693307 | ||||||
| chr5:131693307
|
T | TATATACA others(29): Show |
3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1202+5609_1202+561 others(40): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693307 | ||||||
| chr5:131693309
|
T | TATAC | 7 | a0001c0001t0001g0220a0001c0001t0001g0302a0001c0001t0009g0018others(4): Show | 7 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5607_1202+560 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | ||||||
| chr5:131693309
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0063a0001c0001t0001g0191a0001c0017t0001g0062 | 3 | HG02559.hp2 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | ||||||
| chr5:131693309
|
TATATATA others(17): Show |
T | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202+5584_1202+560 others(28): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | ||||||
| chr5:131693311
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+5606A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | ||||||
| chr5:131693311
|
T | TAC | 22 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0185others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+5605_1202+560 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | ||||||
| chr5:131693311
|
T | TACATATA others(9): Show |
1 | a0001c0001t0001g0222 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1202+5605_1202+560 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | ||||||
| chr5:131693311
|
TATATAC | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(26): Show | 29 | HG00609.hp1 HG00639.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | ||||||
| chr5:131693311
|
TATATACA others(15): Show |
T | 9 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+5584_1202+560 others(26): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | ||||||
| chr5:131693313
|
T | C | 83 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0057others(80): Show | 83 | HG00544.hp1 HG00609.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1202+5604A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693313 | ||||||
| chr5:131693315
|
TAC | T | 63 | a0001c0001t0001g0011a0001c0001t0001g0163a0001c0001t0001g0169others(60): Show | 63 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693315 | ||||||
| chr5:131693317
|
C | T | 133 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(130): Show | 134 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.1202+5600G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693317 | ||||||
| chr5:131693319
|
C | T | 148 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(145): Show | 148 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.1202+5598G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693319 | ||||||
| chr5:131693321
|
T | C | 5 | a0001c0001t0001g0235a0001c0001t0001g0294a0001c0001t0003g0032others(2): Show | 5 | HG00733.hp2 HG01175.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+5596A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693321 | ||||||
| chr5:131693323
|
T | C | 6 | a0001c0001t0001g0220a0001c0001t0009g0018a0001c0001t0009g0044others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+5594A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693323 | ||||||
| chr5:131693325
|
T | C | 22 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0185others(19): Show | 22 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+5592A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693325 | ||||||
| chr5:131693327
|
T | C | 22 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0172others(19): Show | 22 | HG00544.hp1 HG01099.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1202+5590A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693327 | ||||||
| chr5:131693329
|
T | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0163a0001c0001t0001g0169others(64): Show | 67 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1202+5588A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693329 | ||||||
| chr5:131693331
|
T | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0223others(4): Show | 7 | HG01516.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5586A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693331 | ||||||
| chr5:131693333
|
C | CACATATA others(3): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG00738.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1202+5583_1202+558 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CACATATA others(7): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1202+5583_1202+558 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CAT | 27 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0268others(24): Show | 28 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1202+5582_1202+558 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CATAT | 30 | a0001c0001t0001g0209a0001c0001t0002g0083a0001c0001t0002g0085others(27): Show | 31 | HG00408.hp1 HG00738.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1202+5580_1202+558 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CATATAT | 14 | a0001c0001t0002g0084a0001c0001t0002g0086a0001c0001t0002g0090others(11): Show | 14 | HG01123.hp1 HG01261.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1202+5578_1202+558 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CATATATA others(1): Show |
7 | a0001c0001t0002g0149a0001c0001t0002g0151a0001c0001t0006g0054others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5576_1202+558 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | CATATATA others(49): Show |
1 | a0001c0001t0005g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1202+5583_1202+558 others(60): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
C | T | 140 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(137): Show | 140 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.1202+5584G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
CAT | C | 14 | a0001c0001t0001g0063a0001c0001t0001g0262a0001c0001t0008g0301others(11): Show | 14 | HG01261.hp2 HG01433.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202+5582_1202+558 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693333
|
CATATAT | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0260a0002c0002t0002g0156others(1): Show | 4 | HG00544.hp2 HG02165.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+5578_1202+558 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | ||||||
| chr5:131693335
|
T | C | 8 | a0002c0002t0002g0146a0003c0003t0006g0310a0003c0003t0006g0312others(5): Show | 8 | HG00733.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+5582A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | ||||||
| chr5:131693335
|
T | TATATATA others(5): Show |
1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+5581_1202+558 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | ||||||
| chr5:131693335
|
T | TATATATA others(53): Show |
1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1202+5581_1202+558 others(64): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | ||||||
| chr5:131693337
|
T | C | 3 | a0003c0003t0006g0311a0003c0003t0006g0316a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1202+5580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693337 | ||||||
| chr5:131693340
|
A | ATATG | 7 | a0001c0001t0002g0094a0001c0001t0002g0098a0001c0001t0002g0101others(4): Show | 7 | NA18940.hp2 NA18953.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5576_1202+557 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693340 | ||||||
| chr5:131693344
|
A | G | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+5573T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693344 | ||||||
| chr5:131693346
|
A | G | 3 | a0001c0001t0001g0063a0001c0015t0001g0326a0001c0017t0001g0062 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+5571T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693346 | ||||||
| chr5:131693348
|
A | ATATATG | 3 | a0001c0001t0002g0099a0001c0001t0002g0165a0001c0001t0002g0275 | 3 | NA18949.hp1 NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1202+5568_1202+556 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693348 | ||||||
| chr5:131693348
|
A | G | 3 | a0001c0001t0002g0097a0001c0001t0002g0107a0002c0002t0019g0058 | 3 | HG02486.hp2 NA18960.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1202+5569T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693348 | ||||||
| chr5:131693349
|
T | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1202+5568A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693349 | ||||||
| chr5:131693372
|
A | T | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+5545T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693372 | ||||||
| chr5:131693475
|
T | C | 9 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+5442A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693475 | ||||||
| chr5:131693513
|
C | T | 37 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(34): Show | 37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1202+5404G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693513 | ||||||
| chr5:131693770
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.1202+5147T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693770 | ||||||
| chr5:131693866
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+5051C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693866 | ||||||
| chr5:131693990
|
T | C | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1202+4927A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693990 | ||||||
| chr5:131694364
|
T | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+4553A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694364 | ||||||
| chr5:131694392
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1202+4525C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694392 | ||||||
| chr5:131694459
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1202+4458C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694459 | ||||||
| chr5:131694602
|
G | A | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1202+4315C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694602 | ||||||
| chr5:131694635
|
C | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0222others(1): Show | 4 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+4282G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694635 | ||||||
| chr5:131694669
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1202+4248A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694669 | ||||||
| chr5:131694702
|
A | G | 1 | a0001c0001t0008g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1202+4215T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694702 | ||||||
| chr5:131694879
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1202+4038G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694879 | ||||||
| chr5:131695060
|
G | A | 3 | a0001c0001t0003g0025a0001c0001t0003g0029a0001c0001t0023g0228 | 3 | HG01167.hp2 HG01169.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1202+3857C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695060 | ||||||
| chr5:131695104
|
C | CAAAT | 5 | a0001c0001t0002g0081a0002c0002t0002g0003a0002c0002t0002g0288others(2): Show | 5 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+3809_1202+381 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695104
|
C | CAAATAAA others(9): Show |
1 | a0002c0002t0005g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1202+3797_1202+381 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695104
|
CAAAT | C | 178 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(175): Show | 179 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1202+3809_1202+381 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695104
|
CAAATAAA others(1): Show |
C | 93 | a0001c0001t0001g0163a0001c0001t0001g0207a0001c0001t0001g0221others(90): Show | 94 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.1202+3805_1202+381 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695104
|
CAAATAAA others(5): Show |
C | 9 | a0001c0001t0001g0209a0001c0001t0001g0322a0001c0001t0002g0107others(6): Show | 9 | HG01496.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+3801_1202+381 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695104
|
CAAATAAA others(9): Show |
C | 1 | a0002c0002t0002g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+3797_1202+381 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | ||||||
| chr5:131695152
|
T | G | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+3765A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695152 | ||||||
| chr5:131695153
|
A | AAAGC | 4 | a0001c0001t0001g0063a0001c0001t0008g0301a0001c0001t0008g0323others(1): Show | 4 | HG02630.hp1 HG02809.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+3760_1202+376 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | ||||||
| chr5:131695153
|
A | AAATAAAT others(5): Show |
1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1202+3763_1202+376 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | ||||||
| chr5:131695153
|
A | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+3764T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | ||||||
| chr5:131695268
|
T | C | 201 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(198): Show | 201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.1202+3649A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695268 | ||||||
| chr5:131695499
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+3418C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695499 | ||||||
| chr5:131695809
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+3108C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695809 | ||||||
| chr5:131695952
|
G | A | 1 | a0002c0002t0004g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1202+2965C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695952 | ||||||
| chr5:131696140
|
A | G | 3 | a0001c0001t0001g0063a0001c0015t0001g0326a0001c0017t0001g0062 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+2777T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696140 | ||||||
| chr5:131696419
|
TAA | T | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202+2496_1202+249 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696419 | ||||||
| chr5:131696489
|
C | T | 8 | a0001c0001t0006g0054a0001c0001t0006g0069a0001c0005t0001g0066others(5): Show | 8 | HG01081.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+2428G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696489 | ||||||
| chr5:131696717
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0153 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1202+2200C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696717 | ||||||
| chr5:131696875
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0008g0059a0001c0001t0008g0301others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+2042T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696875 | ||||||
| chr5:131696879
|
T | G | 1 | a0004c0007t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1202+2038A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696879 | ||||||
| chr5:131696940
|
G | T | 1 | a0001c0001t0003g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1202+1977C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696940 | ||||||
| chr5:131696952
|
A | G | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1202+1965T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696952 | ||||||
| chr5:131697096
|
T | G | 1 | a0001c0004t0001g0297 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1202+1821A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697096 | ||||||
| chr5:131697122
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+1795C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697122 | ||||||
| chr5:131697191
|
A | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0223a0001c0001t0007g0299others(1): Show | 4 | NA18965.hp2 NA18971.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+1726T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697191 | ||||||
| chr5:131697261
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+1656G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697261 | ||||||
| chr5:131697278
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1202+1639C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697278 | ||||||
| chr5:131697390
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1202+1527T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697390 | ||||||
| chr5:131697527
|
G | A | 1 | a0002c0002t0002g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1202+1390C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697527 | ||||||
| chr5:131697605
|
A | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202+1312T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697605 | ||||||
| chr5:131697704
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1202+1213C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697704 | ||||||
| chr5:131697801
|
A | C | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1202+1116T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697801 | ||||||
| chr5:131697910
|
A | G | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1202+1007T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697910 | ||||||
| chr5:131697932
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+985C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697932 | ||||||
| chr5:131697968
|
C | CA | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 19 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1202+948dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697968 | ||||||
| chr5:131697968
|
CA | C | 57 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0073others(54): Show | 57 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1202+948delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697968 | ||||||
| chr5:131697985
|
A | G | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1202+932T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697985 | ||||||
| chr5:131697989
|
A | G | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+928T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697989 | ||||||
| chr5:131698140
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1202+777T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698140 | ||||||
| chr5:131698207
|
G | C | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1202+710C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698207 | ||||||
| chr5:131698257
|
A | C | 2 | a0001c0001t0008g0022a0001c0001t0008g0074 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+660T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698257 | ||||||
| chr5:131698509
|
G | A | 3 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0048 | 3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1202+408C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698509 | ||||||
| chr5:131699052
|
A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1117-50T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699052 | ||||||
| chr5:131699395
|
C | CT | 55 | a0001c0001t0001g0243a0001c0001t0001g0289a0001c0001t0003g0019others(52): Show | 56 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1117-394dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699395 | ||||||
| chr5:131699443
|
G | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1117-441C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699443 | ||||||
| chr5:131699522
|
T | C | 1 | a0001c0001t0007g0296 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1117-520A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699522 | ||||||
| chr5:131699721
|
G | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1117-719C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699721 | ||||||
| chr5:131699909
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1117-907T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699909 | ||||||
| chr5:131699916
|
C | CA | 7 | a0001c0001t0001g0172a0001c0001t0002g0277a0001c0001t0008g0301others(4): Show | 7 | HG02451.hp1 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-915dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699916
|
C | CAA | 9 | a0001c0001t0001g0008a0001c0001t0001g0173a0001c0001t0001g0175others(6): Show | 9 | HG01993.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-916_1117-915d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699916
|
C | CAAA | 122 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(119): Show | 122 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1117-917_1117-915d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699916
|
C | CAAAA | 16 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0222others(13): Show | 16 | HG00642.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1117-918_1117-915d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699916
|
CAAAAAAA others(3): Show |
C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-924_1117-915d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699916
|
CAAAAAAA others(6): Show |
C | 37 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(34): Show | 37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1117-927_1117-915d others(15): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | ||||||
| chr5:131699983
|
T | C | 3 | a0001c0001t0005g0114a0002c0002t0002g0006a0007c0012t0005g0117 | 3 | HG04115.hp2 NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1117-981A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699983 | ||||||
| chr5:131699999
|
T | C | 1 | a0006c0010t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1117-997A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699999 | ||||||
| chr5:131700280
|
C | T | 1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1117-1278G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700280 | ||||||
| chr5:131700330
|
T | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-1328A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700330 | ||||||
| chr5:131700444
|
G | A | 44 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(41): Show | 44 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1117-1442C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700444 | ||||||
| chr5:131700458
|
T | TA | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1117-1457dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700458 | ||||||
| chr5:131700506
|
C | T | 1 | a0002c0002t0018g0284 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1117-1504G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700506 | ||||||
| chr5:131700545
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1117-1543G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700545 | ||||||
| chr5:131700739
|
T | TA | 13 | a0001c0001t0001g0173a0002c0002t0019g0058a0003c0003t0006g0310others(10): Show | 13 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-1738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700739 | ||||||
| chr5:131700823
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00408.hp2 HG02015.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-1821A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700823 | ||||||
| chr5:131701135
|
T | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1117-2133A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701135 | ||||||
| chr5:131701272
|
T | G | 3 | a0001c0001t0009g0044a0001c0001t0009g0045a0001c0001t0009g0047 | 3 | HG01496.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1117-2270A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701272 | ||||||
| chr5:131701544
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1116+2521C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701544 | ||||||
| chr5:131701723
|
C | T | 1 | a0001c0001t0013g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1116+2342G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701723 | ||||||
| chr5:131701957
|
C | CA | 10 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0006g0054others(7): Show | 10 | HG01081.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1116+2107dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701957 | ||||||
| chr5:131702030
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+2035T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702030 | ||||||
| chr5:131702066
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1116+1999A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702066 | ||||||
| chr5:131702221
|
T | C | 1 | a0002c0002t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1116+1844A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702221 | ||||||
| chr5:131702222
|
G | A | 1 | a0002c0002t0002g0161 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1116+1843C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702222 | ||||||
| chr5:131702739
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1116+1326C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702739 | ||||||
| chr5:131702824
|
C | T | 1 | a0002c0002t0002g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1116+1241G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702824 | ||||||
| chr5:131702938
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1116+1127A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702938 | ||||||
| chr5:131703058
|
T | G | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1116+1007A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703058 | ||||||
| chr5:131703231
|
C | T | 1 | a0001c0001t0012g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1116+834G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703231 | ||||||
| chr5:131703247
|
A | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1116+818T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703247 | ||||||
| chr5:131703399
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1116+666G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703399 | ||||||
| chr5:131703418
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1116+647A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703418 | ||||||
| chr5:131703498
|
A | G | 5 | a0002c0002t0002g0132a0002c0002t0002g0133a0002c0002t0002g0144others(2): Show | 5 | HG01261.hp2 HG01433.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+567T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703498 | ||||||
| chr5:131703673
|
T | C | 13 | a0002c0002t0004g0001a0002c0002t0004g0052a0002c0002t0004g0127others(10): Show | 14 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116+392A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703673 | ||||||
| chr5:131703707
|
C | T | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+358G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703707 | ||||||
| chr5:131703714
|
C | T | 3 | a0002c0002t0002g0158a0002c0002t0002g0159a0002c0002t0002g0281 | 3 | HG01255.hp1 HG01516.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1116+351G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703714 | ||||||
| chr5:131703715
|
G | A | 2 | a0006c0010t0001g0203a0006c0010t0001g0291 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1116+350C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703715 | ||||||
| chr5:131703893
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1116+172A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703893 | ||||||
| chr5:131703935
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1116+130T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703935 | ||||||
| chr5:131703940
|
C | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1116+125G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703940 | ||||||
| chr5:131704612
|
T | C | 9 | a0001c0001t0002g0004a0001c0001t0002g0053a0001c0001t0002g0075others(6): Show | 9 | HG02135.hp2 HG02165.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.915-346A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704612 | ||||||
| chr5:131704812
|
C | T | 1 | a0004c0007t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.915-546G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704812 | ||||||
| chr5:131704859
|
C | T | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(97): Show | 100 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.915-593G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704859 | ||||||
| chr5:131705177
|
A | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.915-911T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705177 | ||||||
| chr5:131705184
|
G | C | 1 | a0001c0001t0001g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.915-918C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705184 | ||||||
| chr5:131705196
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.915-930A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705196 | ||||||
| chr5:131705294
|
C | T | 2 | a0004c0007t0001g0181a0004c0007t0001g0182 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.915-1028G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705294 | ||||||
| chr5:131705380
|
G | A | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.914+1031C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705380 | ||||||
| chr5:131705383
|
G | C | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.914+1028C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705383 | ||||||
| chr5:131705502
|
C | G | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.914+909G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705502 | ||||||
| chr5:131705553
|
C | T | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+858G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705553 | ||||||
| chr5:131705681
|
C | T | 1 | a0001c0001t0005g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.914+730G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705681 | ||||||
| chr5:131705782
|
G | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.914+629C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705782 | ||||||
| chr5:131705897
|
C | T | 201 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(198): Show | 201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.914+514G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705897 | ||||||
| chr5:131705970
|
T | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.914+441A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705970 | ||||||
| chr5:131706031
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131706031 | ||||||
| chr5:131706618
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.779-72T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706618 | ||||||
| chr5:131706725
|
A | G | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.779-179T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706725 | ||||||
| chr5:131706760
|
A | G | 1 | a0002c0002t0002g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.779-214T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706760 | ||||||
| chr5:131707174
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.779-628C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707174 | ||||||
| chr5:131707278
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.779-732G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707278 | ||||||
| chr5:131707296
|
A | G | 2 | a0002c0002t0002g0161a0002c0002t0002g0272 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.779-750T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707296 | ||||||
| chr5:131707513
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-967A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707513 | ||||||
| chr5:131707784
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.779-1238T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707784 | ||||||
| chr5:131707966
|
T | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.778+1235A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707966 | ||||||
| chr5:131707967
|
T | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.778+1234A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707967 | ||||||
| chr5:131708186
|
G | C | 6 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+1015C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708186 | ||||||
| chr5:131708210
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.778+991A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708210 | ||||||
| chr5:131708395
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+806G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708395 | ||||||
| chr5:131708441
|
A | G | 4 | a0001c0001t0001g0302a0004c0007t0001g0174a0004c0007t0001g0181others(1): Show | 4 | HG02976.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+760T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708441 | ||||||
| chr5:131708789
|
G | GA | 6 | a0001c0001t0002g0081a0001c0001t0002g0083a0001c0001t0005g0078others(3): Show | 6 | HG01081.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+411dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708789 | ||||||
| chr5:131708858
|
T | C | 17 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(14): Show | 17 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.778+343A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708858 | ||||||
| chr5:131708898
|
G | GT | 41 | a0001c0001t0001g0063a0001c0001t0001g0163a0001c0001t0003g0019others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.778+302dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708898 | ||||||
| chr5:131708899
|
T | G | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778+302A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708899 | ||||||
| chr5:131709048
|
T | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.778+153A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131709048 | ||||||
| chr5:131709150
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.778+51G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131709150 | ||||||
| chr5:131709390
|
C | A | 2 | a0001c0001t0001g0254a0001c0001t0007g0296 | 2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.707-118G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709390 | ||||||
| chr5:131709575
|
A | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-303T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709575 | ||||||
| chr5:131709699
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01099.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.707-427T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709699 | ||||||
| chr5:131709825
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.707-553T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709825 | ||||||
| chr5:131709849
|
G | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-577C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709849 | ||||||
| chr5:131710078
|
T | G | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.706+500A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710078 | ||||||
| chr5:131710142
|
T | C | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(202): Show | 205 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.706+436A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710142 | ||||||
| chr5:131710337
|
C | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+241G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710337 | ||||||
| chr5:131710496
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.706+82T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710496 | ||||||
| chr5:131710535
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.706+43A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710535 | ||||||
| chr5:131710696
|
G | A | 1 | a0001c0001t0002g0099 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.623-35C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710696 | ||||||
| chr5:131710720
|
G | A | 2 | a0001c0001t0005g0115a0001c0001t0005g0154 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.623-59C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710720 | ||||||
| chr5:131710994
|
A | G | 2 | a0002c0002t0004g0142a0002c0002t0004g0283 | 2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.623-333T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710994 | ||||||
| chr5:131711015
|
T | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.623-354A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711015 | ||||||
| chr5:131711052
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.623-391C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711052 | ||||||
| chr5:131711107
|
A | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.623-446T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711107 | ||||||
| chr5:131711185
|
A | G | 2 | a0002c0002t0002g0288a0002c0002t0005g0126 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.623-524T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711185 | ||||||
| chr5:131711264
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.623-603C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711264 | ||||||
| chr5:131711370
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0153 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.623-709G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711370 | ||||||
| chr5:131711404
|
T | C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.623-743A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711404 | ||||||
| chr5:131711890
|
T | C | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.623-1229A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711890 | ||||||
| chr5:131711928
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.623-1267C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711928 | ||||||
| chr5:131711943
|
A | G | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.623-1282T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711943 | ||||||
| chr5:131712359
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0008g0301 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.623-1698A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712359 | ||||||
| chr5:131712408
|
G | A | 3 | a0002c0002t0002g0158a0002c0002t0002g0159a0002c0002t0002g0281 | 3 | HG01255.hp1 HG01516.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.623-1747C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712408 | ||||||
| chr5:131712429
|
G | A | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.623-1768C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712429 | ||||||
| chr5:131712557
|
C | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.623-1896G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712557 | ||||||
| chr5:131712596
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-1935A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712596 | ||||||
| chr5:131712631
|
A | G | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.623-1970T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712631 | ||||||
| chr5:131713050
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0175a0001c0001t0001g0180others(1): Show | 4 | NA18955.hp2 NA18956.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2389G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713050 | ||||||
| chr5:131713200
|
C | G | 1 | a0001c0001t0005g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.623-2539G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713200 | ||||||
| chr5:131713341
|
C | T | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.623-2680G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713341 | ||||||
| chr5:131713538
|
A | C | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.623-2877T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713538 | ||||||
| chr5:131713589
|
TAAC | T | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.623-2931_623-2929d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713589 | ||||||
| chr5:131713644
|
T | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622+2921A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713644 | ||||||
| chr5:131713703
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.622+2862T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713703 | ||||||
| chr5:131713720
|
C | T | 1 | a0002c0002t0002g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.622+2845G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713720 | ||||||
| chr5:131713785
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.622+2780G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713785 | ||||||
| chr5:131713876
|
G | C | 14 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(11): Show | 14 | NA18945.hp1 NA18947.hp2 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.622+2689C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713876 | ||||||
| chr5:131713884
|
T | A | 1 | a0001c0001t0001g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.622+2681A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713884 | ||||||
| chr5:131713890
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0007g0296 | 2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.622+2675A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713890 | ||||||
| chr5:131713892
|
T | G | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 185 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.622+2673A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713892 | ||||||
| chr5:131714009
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.622+2556G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714009 | ||||||
| chr5:131714244
|
T | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.622+2321A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714244 | ||||||
| chr5:131714264
|
A | G | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.622+2301T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714264 | ||||||
| chr5:131714292
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.622+2273A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714292 | ||||||
| chr5:131714417
|
A | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622+2148T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714417 | ||||||
| chr5:131714517
|
A | C | 1 | a0001c0004t0001g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.622+2048T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714517 | ||||||
| chr5:131714572
|
C | T | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.622+1993G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714572 | ||||||
| chr5:131714652
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622+1913G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714652 | ||||||
| chr5:131714658
|
A | C | 1 | a0001c0001t0005g0154 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.622+1907T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714658 | ||||||
| chr5:131714663
|
T | C | 1 | a0002c0002t0004g0143 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.622+1902A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714663 | ||||||
| chr5:131715087
|
T | G | 43 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0073others(40): Show | 43 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.622+1478A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715087 | ||||||
| chr5:131715221
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622+1344G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715221 | ||||||
| chr5:131715322
|
T | C | 201 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(198): Show | 201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.622+1243A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715322 | ||||||
| chr5:131715343
|
G | A | 4 | a0001c0001t0003g0030a0001c0001t0003g0035a0001c0001t0003g0039others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+1222C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715343 | ||||||
| chr5:131715511
|
C | A | 2 | a0002c0002t0004g0007a0002c0002t0004g0160 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.622+1054G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715511 | ||||||
| chr5:131715585
|
G | A | 325 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 327 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(324): Show |
intron_variant | MODIFIER | c.622+980C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715585 | ||||||
| chr5:131715635
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.622+930T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715635 | ||||||
| chr5:131715714
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.622+851G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715714 | ||||||
| chr5:131715965
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.622+600C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715965 | ||||||
| chr5:131715985
|
T | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715985 | ||||||
| chr5:131716018
|
A | T | 2 | a0001c0001t0002g0088a0001c0001t0002g0120 | 2 | NA19080.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.622+547T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716018 | ||||||
| chr5:131716223
|
T | G | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.622+342A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716223 | ||||||
| chr5:131716286
|
A | C | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.622+279T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716286 | ||||||
| chr5:131716386
|
G | A | 1 | a0001c0004t0001g0297 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.622+179C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716386 | ||||||
| chr5:131716399
|
T | A | 1 | a0001c0001t0009g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+166A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716399 | ||||||
| chr5:131716749
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.531-93G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716749 | ||||||
| chr5:131716868
|
T | C | 1 | a0001c0001t0010g0213 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.531-212A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716868 | ||||||
| chr5:131716977
|
A | T | 1 | a0001c0001t0005g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.531-321T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716977 | ||||||
| chr5:131716979
|
T | A | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-323A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716979 | ||||||
| chr5:131716990
|
T | A | 207 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(204): Show | 207 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.531-334A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716990 | ||||||
| chr5:131716992
|
T | A | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.531-336A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716992 | ||||||
| chr5:131717036
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717036 | ||||||
| chr5:131717151
|
C | T | 4 | a0002c0002t0002g0079a0002c0002t0002g0140a0002c0002t0002g0288others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-495G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717151 | ||||||
| chr5:131717294
|
A | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.531-638T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717294 | ||||||
| chr5:131717359
|
C | T | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.531-703G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717359 | ||||||
| chr5:131717530
|
A | G | 1 | a0001c0001t0008g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.531-874T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717530 | ||||||
| chr5:131717720
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-1064C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717720 | ||||||
| chr5:131718027
|
C | CA | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.530+958dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718027 | ||||||
| chr5:131718027
|
CA | C | 143 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.530+958delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718027 | ||||||
| chr5:131718047
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.530+939G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718047 | ||||||
| chr5:131718048
|
C | T | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530+938G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718048 | ||||||
| chr5:131718064
|
C | T | 1 | a0002c0002t0004g0143 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.530+922G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718064 | ||||||
| chr5:131718065
|
G | A | 1 | a0001c0001t0007g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.530+921C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718065 | ||||||
| chr5:131718077
|
A | G | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.530+909T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718077 | ||||||
| chr5:131718106
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.530+880G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718106 | ||||||
| chr5:131718107
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.530+879C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718107 | ||||||
| chr5:131718163
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.530+823C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718163 | ||||||
| chr5:131718187
|
T | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.530+799A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718187 | ||||||
| chr5:131718641
|
G | A | 2 | a0001c0001t0003g0027a0001c0014t0003g0026 | 2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.530+345C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718641 | ||||||
| chr5:131718691
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.530+295G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718691 | ||||||
| chr5:131719150
|
G | A | 1 | a0001c0004t0001g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.456-90C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 4/17 | chr5 | 131719150 | ||||||
| chr5:131719429
|
C | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.355-12G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719429 | ||||||
| chr5:131719545
|
C | T | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.355-128G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719545 | ||||||
| chr5:131719853
|
T | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.355-436A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719853 | ||||||
| chr5:131719918
|
T | C | 1 | a0002c0002t0002g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.355-501A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719918 | ||||||
| chr5:131720018
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.355-601G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720018 | ||||||
| chr5:131720293
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.355-876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720293 | ||||||
| chr5:131720527
|
A | G | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.355-1110T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720527 | ||||||
| chr5:131720740
|
T | C | 1 | a0001c0001t0007g0263 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.355-1323A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720740 | ||||||
| chr5:131720975
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.355-1558A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720975 | ||||||
| chr5:131721004
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.355-1587C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721004 | ||||||
| chr5:131721116
|
T | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.355-1699A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721116 | ||||||
| chr5:131721175
|
C | T | 1 | a0002c0002t0004g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.355-1758G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721175 | ||||||
| chr5:131721271
|
T | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0270 | 2 | NA18959.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.355-1854A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721271 | ||||||
| chr5:131721274
|
G | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1857C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721274 | ||||||
| chr5:131721333
|
G | A | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.355-1916C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721333 | ||||||
| chr5:131721337
|
T | G | 1 | a0001c0001t0013g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.355-1920A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721337 | ||||||
| chr5:131721416
|
T | A | 1 | a0006c0010t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-1999A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721416 | ||||||
| chr5:131721525
|
G | A | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.355-2108C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721525 | ||||||
| chr5:131721569
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.355-2152G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721569 | ||||||
| chr5:131721689
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.355-2272C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721689 | ||||||
| chr5:131721690
|
C | T | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.355-2273G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721690 | ||||||
| chr5:131721697
|
C | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-2280G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721697 | ||||||
| chr5:131722006
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.355-2589C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722006 | ||||||
| chr5:131722206
|
A | T | 1 | a0002c0002t0002g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-2789T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722206 | ||||||
| chr5:131722243
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355-2826T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722243 | ||||||
| chr5:131722337
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0153 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.355-2920G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722337 | ||||||
| chr5:131722338
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.355-2921C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722338 | ||||||
| chr5:131722384
|
C | G | 1 | a0006c0010t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-2967G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722384 | ||||||
| chr5:131722645
|
C | T | 46 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(43): Show | 46 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.355-3228G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722645 | ||||||
| chr5:131722674
|
C | T | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.355-3257G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722674 | ||||||
| chr5:131722883
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.355-3466T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722883 | ||||||
| chr5:131723053
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.355-3636A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723053 | ||||||
| chr5:131723073
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.355-3656T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723073 | ||||||
| chr5:131723093
|
A | C | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.355-3676T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723093 | ||||||
| chr5:131723379
|
A | T | 1 | a0001c0001t0007g0263 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.355-3962T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723379 | ||||||
| chr5:131723429
|
G | A | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.355-4012C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723429 | ||||||
| chr5:131723483
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0005g0080 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.355-4066T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723483 | ||||||
| chr5:131723619
|
T | G | 37 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(34): Show | 37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.355-4202A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723619 | ||||||
| chr5:131723709
|
A | T | 1 | a0001c0001t0005g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.355-4292T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723709 | ||||||
| chr5:131724099
|
C | T | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.355-4682G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724099 | ||||||
| chr5:131724215
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-4798C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724215 | ||||||
| chr5:131724419
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.355-5002G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724419 | ||||||
| chr5:131724629
|
CAA | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0322 | 3 | HG00738.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.355-5214_355-5213d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724629 | ||||||
| chr5:131724769
|
TTTGCCTA others(20): Show |
T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0289 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.355-5379_355-5353d others(29): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724769 | ||||||
| chr5:131724799
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.355-5382C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724799 | ||||||
| chr5:131724841
|
G | A | 1 | a0002c0002t0002g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.355-5424C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724841 | ||||||
| chr5:131725063
|
T | G | 37 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(34): Show | 37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.355-5646A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725063 | ||||||
| chr5:131725140
|
C | A | 1 | a0001c0004t0001g0061 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.355-5723G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725140 | ||||||
| chr5:131725418
|
A | C | 278 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(275): Show | 279 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(276): Show |
intron_variant | MODIFIER | c.354+5486T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725418 | ||||||
| chr5:131725746
|
G | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.354+5158C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725746 | ||||||
| chr5:131725800
|
G | A | 1 | a0001c0014t0003g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.354+5104C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725800 | ||||||
| chr5:131725811
|
C | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.354+5093G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725811 | ||||||
| chr5:131725914
|
T | C | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.354+4990A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725914 | ||||||
| chr5:131725987
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+4917C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725987 | ||||||
| chr5:131726133
|
A | G | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+4771T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726133 | ||||||
| chr5:131726343
|
C | A | 2 | a0001c0001t0002g0149a0001c0001t0002g0151 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.354+4561G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726343 | ||||||
| chr5:131726714
|
T | C | 17 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0185others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+4190A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726714 | ||||||
| chr5:131726889
|
C | T | 2 | a0001c0008t0002g0110a0001c0008t0002g0285 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.354+4015G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726889 | ||||||
| chr5:131726949
|
T | C | 4 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074others(1): Show | 4 | HG02109.hp2 HG02145.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+3955A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726949 | ||||||
| chr5:131727356
|
C | A | 1 | a0001c0001t0007g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.354+3548G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727356 | ||||||
| chr5:131727380
|
C | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.354+3524G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727380 | ||||||
| chr5:131727386
|
C | A | 2 | a0002c0002t0004g0131a0002c0002t0004g0287 | 2 | NA18978.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.354+3518G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727386 | ||||||
| chr5:131727660
|
G | A | 11 | a0001c0001t0001g0055a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.354+3244C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727660 | ||||||
| chr5:131727676
|
T | C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+3228A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727676 | ||||||
| chr5:131728000
|
T | C | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.354+2904A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728000 | ||||||
| chr5:131728041
|
G | A | 5 | a0001c0001t0008g0059a0001c0001t0008g0301a0001c0001t0008g0323others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+2863C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728041 | ||||||
| chr5:131728143
|
C | T | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+2761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728143 | ||||||
| chr5:131728289
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.354+2615A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728289 | ||||||
| chr5:131728725
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+2179G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728725 | ||||||
| chr5:131728882
|
T | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0188a0001c0001t0001g0215others(2): Show | 5 | HG00733.hp1 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+2022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728882 | ||||||
| chr5:131728943
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.354+1961G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728943 | ||||||
| chr5:131729092
|
G | A | 1 | a0002c0002t0002g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.354+1812C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729092 | ||||||
| chr5:131729144
|
G | T | 5 | a0001c0001t0002g0097a0001c0001t0002g0099a0001c0001t0002g0107others(2): Show | 5 | NA18949.hp1 NA18951.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+1760C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729144 | ||||||
| chr5:131729157
|
G | C | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.354+1747C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729157 | ||||||
| chr5:131729194
|
T | A | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.354+1710A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729194 | ||||||
| chr5:131729249
|
G | A | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.354+1655C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729249 | ||||||
| chr5:131729291
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.354+1613G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729291 | ||||||
| chr5:131729862
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0074 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+1042G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729862 | ||||||
| chr5:131730229
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.354+675G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730229 | ||||||
| chr5:131730411
|
G | C | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.354+493C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730411 | ||||||
| chr5:131730640
|
AAG | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+262_354+263del others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730640 | ||||||
| chr5:131730884
|
A | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.354+20T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730884 | ||||||
| chr5:131731160
|
T | A | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-122A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731160 | ||||||
| chr5:131731206
|
C | A | 6 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-168G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731206 | ||||||
| chr5:131731300
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.220-262C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731300 | ||||||
| chr5:131731641
|
C | CA | 41 | a0001c0001t0002g0098a0001c0001t0002g0122a0001c0001t0003g0019others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.220-604dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731641 | ||||||
| chr5:131731653
|
C | A | 1 | a0001c0005t0007g0070 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.220-615G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731653 | ||||||
| chr5:131731851
|
T | TA | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-814dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731851 | ||||||
| chr5:131731970
|
T | G | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-932A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731970 | ||||||
| chr5:131732166
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-1128A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732166 | ||||||
| chr5:131732245
|
C | A | 1 | a0001c0013t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-1207G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732245 | ||||||
| chr5:131732402
|
C | G | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(97): Show | 100 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.220-1364G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732402 | ||||||
| chr5:131732553
|
G | C | 34 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(31): Show | 34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.220-1515C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732553 | ||||||
| chr5:131732554
|
C | T | 4 | a0002c0002t0004g0128a0002c0002t0004g0139a0002c0002t0004g0155others(1): Show | 4 | NA18962.hp2 NA18984.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-1516G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732554 | ||||||
| chr5:131732669
|
T | G | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1631A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732669 | ||||||
| chr5:131732670
|
T | C | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1632A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732670 | ||||||
| chr5:131732671
|
A | T | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1633T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732671 | ||||||
| chr5:131732716
|
G | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1678C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732716 | ||||||
| chr5:131732807
|
T | G | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-1769A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732807 | ||||||
| chr5:131733102
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-2064C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733102 | ||||||
| chr5:131733150
|
G | A | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-2112C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733150 | ||||||
| chr5:131733168
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.220-2130G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733168 | ||||||
| chr5:131733277
|
G | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-2239C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733277 | ||||||
| chr5:131733349
|
C | G | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-2311G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733349 | ||||||
| chr5:131733371
|
T | C | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.220-2333A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733371 | ||||||
| chr5:131733500
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2462G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733500 | ||||||
| chr5:131733502
|
C | T | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220-2464G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733502 | ||||||
| chr5:131733506
|
G | A | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.220-2468C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733506 | ||||||
| chr5:131733645
|
A | G | 1 | a0001c0001t0010g0213 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.220-2607T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733645 | ||||||
| chr5:131733759
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2721T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733759 | ||||||
| chr5:131733771
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.220-2733C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733771 | ||||||
| chr5:131733786
|
T | C | 1 | a0002c0002t0002g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220-2748A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733786 | ||||||
| chr5:131733850
|
A | T | 1 | a0001c0001t0002g0122 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.220-2812T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733850 | ||||||
| chr5:131734115
|
G | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-3077C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734115 | ||||||
| chr5:131734159
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.220-3121G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734159 | ||||||
| chr5:131734320
|
T | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-3282A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734320 | ||||||
| chr5:131734337
|
CTGA | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-3302_220-3300d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734337 | ||||||
| chr5:131734409
|
TC | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-3372delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734409 | ||||||
| chr5:131734484
|
T | C | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-3446A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734484 | ||||||
| chr5:131734544
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.220-3506A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734544 | ||||||
| chr5:131734593
|
A | T | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3555T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734593 | ||||||
| chr5:131734627
|
C | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-3589G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734627 | ||||||
| chr5:131734630
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-3592G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734630 | ||||||
| chr5:131734657
|
G | A | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3619C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734657 | ||||||
| chr5:131734786
|
G | A | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220-3748C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734786 | ||||||
| chr5:131735009
|
C | T | 10 | a0001c0001t0008g0059a0001c0001t0008g0301a0001c0001t0008g0323others(7): Show | 10 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-3971G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735009 | ||||||
| chr5:131735165
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.220-4127G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735165 | ||||||
| chr5:131735210
|
C | CA | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-4173dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735210 | ||||||
| chr5:131735259
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-4221A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735259 | ||||||
| chr5:131735284
|
G | A | 2 | a0002c0002t0004g0155a0002c0002t0004g0162 | 2 | NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.220-4246C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735284 | ||||||
| chr5:131735324
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-4286C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735324 | ||||||
| chr5:131735404
|
G | C | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.220-4366C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735404 | ||||||
| chr5:131735454
|
A | ATTTTATA others(7): Show |
1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-4417_220-4416i others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735454 | ||||||
| chr5:131735454
|
A | ATTTTATA others(7): Show |
324 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(321): Show | 326 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(323): Show |
intron_variant | MODIFIER | c.220-4417_220-4416i others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735454 | ||||||
| chr5:131735474
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-4436A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735474 | ||||||
| chr5:131735494
|
C | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-4456G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735494 | ||||||
| chr5:131735502
|
A | G | 1 | a0006c0010t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-4464T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735502 | ||||||
| chr5:131735553
|
C | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 151 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.220-4515G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735553 | ||||||
| chr5:131735588
|
G | A | 1 | a0001c0005t0007g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.220-4550C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735588 | ||||||
| chr5:131735612
|
A | T | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.220-4574T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735612 | ||||||
| chr5:131735625
|
TGTATACG others(7): Show |
T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-4601_220-4588d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735625 | ||||||
| chr5:131735640
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-4602C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735640 | ||||||
| chr5:131735747
|
A | T | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0055others(97): Show | 100 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.220-4709T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735747 | ||||||
| chr5:131735787
|
A | C | 4 | a0002c0002t0004g0128a0002c0002t0004g0139a0002c0002t0004g0155others(1): Show | 4 | NA18962.hp2 NA18984.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-4749T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735787 | ||||||
| chr5:131735807
|
A | ATG | 7 | a0001c0001t0001g0219a0001c0001t0001g0223a0001c0001t0003g0037others(4): Show | 7 | HG00642.hp1 HG01496.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-4771_220-4770d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735807 | ||||||
| chr5:131735807
|
ATG | A | 14 | a0001c0001t0003g0019a0001c0001t0006g0054a0001c0001t0008g0301others(11): Show | 14 | HG01081.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-4771_220-4770d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735807 | ||||||
| chr5:131735825
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.220-4787C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735825 | ||||||
| chr5:131735929
|
C | G | 4 | a0002c0002t0002g0123a0002c0002t0002g0161a0002c0002t0002g0272others(1): Show | 4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4891G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735929 | ||||||
| chr5:131736474
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.220-5436C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736474 | ||||||
| chr5:131736717
|
C | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.220-5679G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736717 | ||||||
| chr5:131736804
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0183 | 2 | NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.220-5766G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736804 | ||||||
| chr5:131736846
|
T | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-5808A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736846 | ||||||
| chr5:131736869
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.220-5831G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736869 | ||||||
| chr5:131736916
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.220-5878C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736916 | ||||||
| chr5:131736929
|
A | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.220-5891T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736929 | ||||||
| chr5:131736988
|
A | C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-5950T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736988 | ||||||
| chr5:131737056
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-6018C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737056 | ||||||
| chr5:131737220
|
C | G | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-6182G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737220 | ||||||
| chr5:131737258
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0278 | 3 | HG01109.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.220-6220G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737258 | ||||||
| chr5:131737345
|
T | A | 1 | a0001c0001t0005g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.220-6307A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737345 | ||||||
| chr5:131737672
|
C | T | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-6634G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737672 | ||||||
| chr5:131737712
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-6674G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737712 | ||||||
| chr5:131737786
|
T | TA | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-6749_220-6748i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737786 | ||||||
| chr5:131738309
|
G | C | 2 | a0001c0001t0002g0088a0001c0001t0002g0120 | 2 | NA19080.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.219+6255C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738309 | ||||||
| chr5:131738483
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+6081A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738483 | ||||||
| chr5:131738504
|
C | A | 21 | a0002c0002t0002g0003a0002c0002t0002g0005a0002c0002t0002g0006others(18): Show | 21 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+6060G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738504 | ||||||
| chr5:131738610
|
G | A | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.219+5954C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738610 | ||||||
| chr5:131738658
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+5906G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738658 | ||||||
| chr5:131738660
|
C | T | 1 | a0003c0003t0006g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+5904G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738660 | ||||||
| chr5:131738812
|
CT | C | 59 | a0001c0001t0002g0093a0001c0001t0003g0019a0001c0001t0003g0020others(56): Show | 59 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+5751delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738812 | ||||||
| chr5:131739008
|
G | T | 1 | a0001c0001t0002g0084 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.219+5556C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739008 | ||||||
| chr5:131739289
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.219+5275G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739289 | ||||||
| chr5:131739326
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+5238G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739326 | ||||||
| chr5:131739327
|
G | A | 1 | a0002c0006t0004g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.219+5237C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739327 | ||||||
| chr5:131739356
|
T | C | 1 | a0001c0001t0022g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.219+5208A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739356 | ||||||
| chr5:131739477
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+5087G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739477 | ||||||
| chr5:131739579
|
C | T | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4985G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739579 | ||||||
| chr5:131739760
|
C | G | 3 | a0001c0001t0008g0059a0001c0001t0008g0323a0001c0001t0008g0324 | 3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.219+4804G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739760 | ||||||
| chr5:131739769
|
C | T | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4795G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739769 | ||||||
| chr5:131739773
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219+4791C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739773 | ||||||
| chr5:131739812
|
C | CA | 41 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0176others(38): Show | 41 | HG00438.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.219+4751dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | ||||||
| chr5:131739812
|
CA | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0006g0054others(6): Show | 9 | HG01081.hp1 HG01496.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+4751delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | ||||||
| chr5:131739812
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+4741_219+4751d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | ||||||
| chr5:131739824
|
A | C | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219+4740T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739824 | ||||||
| chr5:131739832
|
A | AC | 4 | a0001c0001t0003g0034a0001c0001t0003g0038a0001c0001t0003g0048others(1): Show | 4 | HG00642.hp1 HG01071.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+4731_219+4732i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739832 | ||||||
| chr5:131739832
|
A | C | 26 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(23): Show | 26 | HG00639.hp1 HG01069.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.219+4732T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739832 | ||||||
| chr5:131739833
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0200 | 2 | NA18979.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.219+4731T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739833 | ||||||
| chr5:131739835
|
A | C | 6 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01934.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+4729T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739835 | ||||||
| chr5:131739837
|
A | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+4727T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739837 | ||||||
| chr5:131739934
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.219+4630A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739934 | ||||||
| chr5:131740165
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+4399G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740165 | ||||||
| chr5:131740228
|
C | T | 277 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(274): Show | 278 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.219+4336G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740228 | ||||||
| chr5:131740374
|
A | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4190T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740374 | ||||||
| chr5:131740496
|
G | C | 1 | a0001c0001t0006g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219+4068C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740496 | ||||||
| chr5:131740531
|
T | A | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.219+4033A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740531 | ||||||
| chr5:131740577
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219+3987C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740577 | ||||||
| chr5:131740983
|
T | TA | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+3580dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740983 | ||||||
| chr5:131741173
|
A | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+3391T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741173 | ||||||
| chr5:131741498
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.219+3066A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741498 | ||||||
| chr5:131741635
|
T | C | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+2929A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741635 | ||||||
| chr5:131741827
|
C | T | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219+2737G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741827 | ||||||
| chr5:131741869
|
C | T | 7 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+2695G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741869 | ||||||
| chr5:131742016
|
C | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.219+2548G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742016 | ||||||
| chr5:131742212
|
C | A | 19 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0002g0152others(16): Show | 19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+2352G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742212 | ||||||
| chr5:131742273
|
G | A | 1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.219+2291C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742273 | ||||||
| chr5:131742335
|
A | G | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.219+2229T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742335 | ||||||
| chr5:131742340
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+2224A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742340 | ||||||
| chr5:131742441
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.219+2123G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742441 | ||||||
| chr5:131742637
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+1927G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742637 | ||||||
| chr5:131742645
|
T | C | 3 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0318 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219+1919A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742645 | ||||||
| chr5:131742805
|
C | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 151 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.219+1759G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742805 | ||||||
| chr5:131742993
|
G | A | 3 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0048 | 3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+1571C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742993 | ||||||
| chr5:131743046
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+1518C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743046 | ||||||
| chr5:131743062
|
T | C | 2 | a0001c0001t0002g0149a0001c0001t0002g0151 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.219+1502A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743062 | ||||||
| chr5:131743328
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+1236G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743328 | ||||||
| chr5:131743595
|
T | C | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.219+969A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743595 | ||||||
| chr5:131743614
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+950G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743614 | ||||||
| chr5:131743863
|
G | T | 2 | a0006c0010t0001g0203a0006c0010t0001g0291 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.219+701C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743863 | ||||||
| chr5:131743888
|
C | G | 1 | a0001c0001t0007g0240 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.219+676G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743888 | ||||||
| chr5:131744036
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.219+528C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131744036 | ||||||
| chr5:131744115
|
C | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.219+449G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131744115 | ||||||
| chr5:131744808
|
A | AAT | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-120_93-119dupAT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744808 | ||||||
| chr5:131744913
|
C | G | 1 | a0002c0002t0002g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.93-223G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744913 | ||||||
| chr5:131744993
|
T | C | 1 | a0002c0002t0004g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.93-303A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744993 | ||||||
| chr5:131745074
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.93-384G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745074 | ||||||
| chr5:131745267
|
C | T | 17 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0185others(14): Show | 17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.93-577G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745267 | ||||||
| chr5:131745288
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93-598C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745288 | ||||||
| chr5:131745436
|
C | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745436 | ||||||
| chr5:131745460
|
T | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-770A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745460 | ||||||
| chr5:131745577
|
T | A | 1 | a0006c0010t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.93-887A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745577 | ||||||
| chr5:131745591
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.93-901A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745591 | ||||||
| chr5:131745620
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-930A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745620 | ||||||
| chr5:131745673
|
G | A | 3 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0048 | 3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93-983C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745673 | ||||||
| chr5:131745695
|
A | C | 1 | a0004c0007t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.93-1005T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745695 | ||||||
| chr5:131745761
|
T | A | 1 | a0001c0001t0003g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.93-1071A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745761 | ||||||
| chr5:131745833
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93-1143G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745833 | ||||||
| chr5:131745961
|
T | G | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-1271A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745961 | ||||||
| chr5:131746203
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-1513C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746203 | ||||||
| chr5:131746384
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.93-1694T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746384 | ||||||
| chr5:131746419
|
C | T | 1 | a0001c0001t0005g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.93-1729G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746419 | ||||||
| chr5:131746520
|
T | C | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-1830A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746520 | ||||||
| chr5:131746962
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-2272A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746962 | ||||||
| chr5:131746994
|
A | G | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93-2304T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746994 | ||||||
| chr5:131747393
|
A | G | 1 | a0001c0001t0005g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.93-2703T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747393 | ||||||
| chr5:131747585
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-2895G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747585 | ||||||
| chr5:131747886
|
A | G | 1 | a0002c0002t0002g0148 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.93-3196T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747886 | ||||||
| chr5:131747889
|
G | A | 1 | a0002c0002t0002g0148 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.93-3199C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747889 | ||||||
| chr5:131748136
|
T | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.93-3446A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748136 | ||||||
| chr5:131748173
|
T | C | 9 | a0002c0002t0004g0001a0002c0002t0004g0127a0002c0002t0004g0136others(6): Show | 10 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-3483A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748173 | ||||||
| chr5:131748453
|
G | C | 1 | a0001c0005t0007g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93-3763C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748453 | ||||||
| chr5:131748479
|
G | A | 1 | a0002c0002t0002g0288 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.93-3789C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748479 | ||||||
| chr5:131748549
|
T | C | 1 | a0001c0001t0010g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.93-3859A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748549 | ||||||
| chr5:131748566
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.93-3876T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748566 | ||||||
| chr5:131748630
|
G | C | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-3940C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748630 | ||||||
| chr5:131748691
|
T | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-4001A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748691 | ||||||
| chr5:131748696
|
C | CA | 182 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(179): Show | 182 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.93-4007dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748696 | ||||||
| chr5:131748709
|
G | A | 10 | a0001c0001t0001g0163a0001c0001t0003g0019a0001c0001t0003g0037others(7): Show | 10 | HG00642.hp1 HG02258.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-4019C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748709 | ||||||
| chr5:131748709
|
GA | G | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-4020delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748709 | ||||||
| chr5:131748710
|
A | G | 8 | a0001c0001t0003g0019a0001c0001t0003g0037a0001c0001t0003g0040others(5): Show | 8 | HG00642.hp1 HG02258.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-4020T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748710 | ||||||
| chr5:131748752
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-4062A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748752 | ||||||
| chr5:131748786
|
C | T | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-4096G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748786 | ||||||
| chr5:131748935
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-4245A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748935 | ||||||
| chr5:131749065
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.93-4375A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749065 | ||||||
| chr5:131749233
|
C | G | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-4543G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749233 | ||||||
| chr5:131749293
|
T | G | 1 | a0001c0001t0002g0277 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.93-4603A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749293 | ||||||
| chr5:131749309
|
G | A | 1 | a0001c0001t0003g0304 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.93-4619C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749309 | ||||||
| chr5:131749621
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.93-4931T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749621 | ||||||
| chr5:131750051
|
T | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-5361A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750051 | ||||||
| chr5:131750057
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.93-5367C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750057 | ||||||
| chr5:131750286
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.93-5596T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750286 | ||||||
| chr5:131750288
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93-5598C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750288 | ||||||
| chr5:131750492
|
T | C | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.93-5802A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750492 | ||||||
| chr5:131750616
|
C | CT | 24 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(21): Show | 24 | HG01496.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.93-5927dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | ||||||
| chr5:131750616
|
C | CTT | 31 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-5928_93-5927dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | ||||||
| chr5:131750616
|
CT | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0293others(3): Show | 6 | HG01069.hp1 HG01168.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-5927delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | ||||||
| chr5:131750638
|
A | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-5948T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750638 | ||||||
| chr5:131750882
|
C | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6192G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750882 | ||||||
| chr5:131750924
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.93-6234T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750924 | ||||||
| chr5:131750955
|
T | C | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.93-6265A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750955 | ||||||
| chr5:131751078
|
G | C | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.93-6388C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751078 | ||||||
| chr5:131751129
|
C | A | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-6439G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751129 | ||||||
| chr5:131751187
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-6497T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751187 | ||||||
| chr5:131751244
|
C | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-6554G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751244 | ||||||
| chr5:131751251
|
A | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-6561T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751251 | ||||||
| chr5:131751341
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-6651G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751341 | ||||||
| chr5:131751487
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-6797C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751487 | ||||||
| chr5:131751571
|
G | GA | 7 | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0106others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6882dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751571 | ||||||
| chr5:131751571
|
GA | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0260a0001c0001t0008g0301others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6882delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751571 | ||||||
| chr5:131751703
|
T | C | 1 | a0001c0001t0008g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.93-7013A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751703 | ||||||
| chr5:131751762
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.93-7072C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751762 | ||||||
| chr5:131751921
|
C | G | 1 | a0001c0001t0003g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93-7231G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751921 | ||||||
| chr5:131751953
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-7263A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751953 | ||||||
| chr5:131751963
|
T | C | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.93-7273A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751963 | ||||||
| chr5:131752037
|
G | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-7347C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752037 | ||||||
| chr5:131752101
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0020g0231 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.93-7411A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752101 | ||||||
| chr5:131752174
|
G | T | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.93-7484C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752174 | ||||||
| chr5:131752538
|
T | TA | 154 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(151): Show | 154 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.93-7849dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752538 | ||||||
| chr5:131752538
|
T | TAA | 35 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0223others(32): Show | 35 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.93-7850_93-7849dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752538 | ||||||
| chr5:131752779
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.93-8089A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752779 | ||||||
| chr5:131752793
|
C | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.93-8103G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752793 | ||||||
| chr5:131752807
|
C | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-8117G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752807 | ||||||
| chr5:131752884
|
A | G | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-8194T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752884 | ||||||
| chr5:131753138
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.93-8448C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753138 | ||||||
| chr5:131753142
|
C | T | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-8452G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753142 | ||||||
| chr5:131753306
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0225 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.93-8616C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753306 | ||||||
| chr5:131753341
|
T | G | 38 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(35): Show | 38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.93-8651A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753341 | ||||||
| chr5:131753351
|
A | C | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-8661T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753351 | ||||||
| chr5:131753386
|
G | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-8696C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753386 | ||||||
| chr5:131753409
|
T | C | 2 | a0002c0002t0002g0161a0002c0002t0002g0272 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.93-8719A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753409 | ||||||
| chr5:131753540
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.93-8850T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753540 | ||||||
| chr5:131753574
|
G | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(15): Show | 18 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.93-8884C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753574 | ||||||
| chr5:131753612
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0005g0080 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.93-8922A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753612 | ||||||
| chr5:131753664
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.93-8974A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753664 | ||||||
| chr5:131753817
|
A | AT | 6 | a0001c0001t0001g0233a0001c0001t0002g0004a0001c0001t0002g0098others(3): Show | 6 | NA18956.hp2 NA18978.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-9128dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753817 | ||||||
| chr5:131753848
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-9158A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753848 | ||||||
| chr5:131753971
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-9281C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753971 | ||||||
| chr5:131754176
|
C | CT | 278 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(275): Show | 279 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.93-9487dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754176 | ||||||
| chr5:131754393
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0002g0107 | 2 | HG02896.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.93-9703G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754393 | ||||||
| chr5:131754518
|
G | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-9828C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754518 | ||||||
| chr5:131754626
|
G | C | 1 | a0001c0001t0021g0012 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.93-9936C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754626 | ||||||
| chr5:131754749
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10059T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754749 | ||||||
| chr5:131754787
|
T | C | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93-10097A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754787 | ||||||
| chr5:131754833
|
G | A | 1 | a0002c0002t0002g0281 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.93-10143C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754833 | ||||||
| chr5:131755143
|
G | A | 2 | a0001c0001t0005g0077a0001c0001t0005g0113 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.93-10453C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755143 | ||||||
| chr5:131755301
|
A | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00408.hp2 HG02015.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-10611T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755301 | ||||||
| chr5:131755378
|
G | A | 144 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.93-10688C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755378 | ||||||
| chr5:131755396
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-10706T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755396 | ||||||
| chr5:131755420
|
T | TA | 44 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0073others(41): Show | 44 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.93-10731dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755420 | ||||||
| chr5:131755435
|
C | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10745G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755435 | ||||||
| chr5:131755452
|
A | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-10762T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755452 | ||||||
| chr5:131755646
|
A | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10956T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755646 | ||||||
| chr5:131756038
|
A | G | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-11348T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756038 | ||||||
| chr5:131756696
|
G | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-12006C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756696 | ||||||
| chr5:131756780
|
T | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-12090A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756780 | ||||||
| chr5:131757002
|
G | A | 2 | a0002c0002t0004g0007a0002c0002t0004g0160 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.93-12312C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757002 | ||||||
| chr5:131757176
|
T | C | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-12486A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757176 | ||||||
| chr5:131757290
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.93-12600C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757290 | ||||||
| chr5:131757346
|
A | T | 4 | a0002c0002t0002g0079a0002c0002t0002g0140a0002c0002t0002g0288others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-12656T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757346 | ||||||
| chr5:131758082
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-13392C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758082 | ||||||
| chr5:131758276
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.93-13586C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758276 | ||||||
| chr5:131758286
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.93-13596G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758286 | ||||||
| chr5:131758324
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-13634G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758324 | ||||||
| chr5:131758479
|
A | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-13789T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758479 | ||||||
| chr5:131758709
|
A | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-14019T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758709 | ||||||
| chr5:131758756
|
G | A | 19 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0002g0152others(16): Show | 19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-14066C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758756 | ||||||
| chr5:131758883
|
G | A | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-14193C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758883 | ||||||
| chr5:131758926
|
C | G | 3 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0029 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.93-14236G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758926 | ||||||
| chr5:131759020
|
T | A | 1 | a0002c0002t0004g0162 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.93-14330A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759020 | ||||||
| chr5:131759299
|
ACAGAGAA others(21): Show |
A | 1 | a0001c0001t0010g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.93-14637_93-14610d others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759299 | ||||||
| chr5:131759447
|
T | C | 41 | a0001c0001t0001g0063a0001c0001t0003g0019a0001c0001t0003g0020others(38): Show | 41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.93-14757A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759447 | ||||||
| chr5:131759614
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-14924C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759614 | ||||||
| chr5:131759616
|
G | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-14926C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759616 | ||||||
| chr5:131759827
|
G | C | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-15137C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759827 | ||||||
| chr5:131759836
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.93-15146G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759836 | ||||||
| chr5:131759900
|
T | C | 1 | a0004c0007t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.93-15210A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759900 | ||||||
| chr5:131759944
|
G | T | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.93-15254C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759944 | ||||||
| chr5:131760272
|
T | C | 1 | a0001c0001t0005g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.93-15582A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760272 | ||||||
| chr5:131760456
|
T | G | 1 | a0001c0001t0013g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93-15766A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760456 | ||||||
| chr5:131760590
|
T | G | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.93-15900A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760590 | ||||||
| chr5:131760775
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-16085G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760775 | ||||||
| chr5:131760955
|
C | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-16265G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760955 | ||||||
| chr5:131760984
|
C | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-16294G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760984 | ||||||
| chr5:131761088
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-16398G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761088 | ||||||
| chr5:131761157
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-16467T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761157 | ||||||
| chr5:131761640
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-16950C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761640 | ||||||
| chr5:131762527
|
G | A | 51 | a0001c0001t0002g0274a0001c0001t0005g0049a0002c0002t0002g0003others(48): Show | 52 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.93-17837C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762527 | ||||||
| chr5:131762604
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-17914C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762604 | ||||||
| chr5:131762853
|
A | G | 19 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0002g0152others(16): Show | 19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-18163T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762853 | ||||||
| chr5:131763113
|
G | T | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-18423C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763113 | ||||||
| chr5:131763288
|
T | TAC | 52 | a0001c0001t0002g0075a0001c0001t0002g0081a0001c0001t0002g0101others(49): Show | 53 | HG00408.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.93-18600_93-18599d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
T | TACAC | 54 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0053others(51): Show | 55 | HG00544.hp2 HG00738.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.93-18602_93-18599d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
T | TACACAC | 11 | a0001c0001t0002g0089a0001c0001t0002g0097a0001c0001t0002g0099others(8): Show | 11 | HG02015.hp1 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-18604_93-18599d others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
T | TACACACA others(1): Show |
15 | a0001c0001t0001g0302a0001c0001t0002g0153a0001c0001t0003g0024others(12): Show | 15 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.93-18606_93-18599d others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
T | TACACACA others(3): Show |
3 | a0001c0001t0003g0028a0001c0001t0003g0308a0001c0001t0013g0043 | 3 | HG00639.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.93-18608_93-18599d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
T | TACACACA others(5): Show |
1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.93-18610_93-18599d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
TAC | T | 5 | a0001c0001t0001g0063a0001c0001t0002g0108a0001c0017t0001g0062others(2): Show | 5 | HG00438.hp1 HG02135.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-18600_93-18599d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
TACAC | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-18602_93-18599d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-18610_93-18599d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
TACACACA others(7): Show |
T | 143 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.93-18612_93-18599d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763288
|
TACACACA others(9): Show |
T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-18614_93-18599d others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | ||||||
| chr5:131763349
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0008g0022a0001c0001t0008g0023others(1): Show | 4 | HG01123.hp2 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-18659A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763349 | ||||||
| chr5:131763413
|
T | C | 48 | a0001c0001t0001g0063a0001c0001t0001g0302a0001c0001t0003g0019others(45): Show | 48 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.93-18723A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763413 | ||||||
| chr5:131763453
|
T | C | 39 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(36): Show | 39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.93-18763A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763453 | ||||||
| chr5:131763534
|
C | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.93-18844G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763534 | ||||||
| chr5:131764100
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0007g0296 | 2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.93-19410G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764100 | ||||||
| chr5:131764181
|
A | C | 1 | a0003c0003t0006g0311 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.93-19491T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764181 | ||||||
| chr5:131764307
|
C | CT | 11 | a0001c0001t0001g0184a0001c0001t0001g0199a0001c0001t0002g0098others(8): Show | 11 | HG01496.hp1 HG02015.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-19618dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | ||||||
| chr5:131764307
|
C | CTT | 9 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0222others(6): Show | 9 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.93-19619_93-19618d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | ||||||
| chr5:131764307
|
CT | C | 17 | a0001c0001t0001g0180a0001c0001t0001g0183a0001c0001t0001g0235others(14): Show | 17 | HG00639.hp1 HG02572.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.93-19618delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | ||||||
| chr5:131764432
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-19742C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764432 | ||||||
| chr5:131764447
|
G | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.93-19757C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764447 | ||||||
| chr5:131764553
|
T | C | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.93-19863A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764553 | ||||||
| chr5:131764732
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.93-20042G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764732 | ||||||
| chr5:131765496
|
T | C | 38 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(35): Show | 38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.93-20806A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131765496 | ||||||
| chr5:131766132
|
C | T | 1 | a0002c0002t0004g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.93-21442G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766132 | ||||||
| chr5:131766215
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-21525T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766215 | ||||||
| chr5:131766252
|
G | A | 8 | a0001c0001t0001g0302a0001c0001t0003g0303a0001c0001t0003g0304others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-21562C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766252 | ||||||
| chr5:131766255
|
T | G | 8 | a0001c0001t0001g0302a0001c0001t0003g0303a0001c0001t0003g0304others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-21565A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766255 | ||||||
| chr5:131766291
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.93-21601G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766291 | ||||||
| chr5:131766361
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.93-21671G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766361 | ||||||
| chr5:131766417
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-21727G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766417 | ||||||
| chr5:131766444
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.93-21754C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766444 | ||||||
| chr5:131766501
|
T | C | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.93-21811A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766501 | ||||||
| chr5:131766505
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-21815G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766505 | ||||||
| chr5:131766577
|
G | C | 1 | a0002c0002t0004g0119 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.93-21887C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766577 | ||||||
| chr5:131766869
|
T | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0260a0001c0001t0001g0262 | 3 | HG02165.hp2 HG04184.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.93-22179A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766869 | ||||||
| chr5:131766899
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.93-22209G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766899 | ||||||
| chr5:131766901
|
C | T | 1 | a0003c0003t0006g0311 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.93-22211G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766901 | ||||||
| chr5:131766952
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.93-22262A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766952 | ||||||
| chr5:131767121
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22431A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767121 | ||||||
| chr5:131767129
|
T | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-22439A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767129 | ||||||
| chr5:131767209
|
A | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22519T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767209 | ||||||
| chr5:131767238
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22548G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767238 | ||||||
| chr5:131767277
|
C | T | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-22587G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767277 | ||||||
| chr5:131767361
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.93-22671C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767361 | ||||||
| chr5:131767427
|
C | CA | 9 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0258others(6): Show | 9 | HG01884.hp2 HG01981.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.93-22738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0008g0022a0001c0001t0008g0023 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-22747_93-22738d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0008g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93-22748_93-22738d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CA | C | 183 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(180): Show | 185 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.93-22738delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAA | C | 8 | a0001c0001t0001g0057a0001c0001t0001g0185a0001c0001t0001g0209others(5): Show | 8 | HG01069.hp1 HG01256.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-22739_93-22738d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAAA | C | 11 | a0001c0001t0006g0054a0003c0003t0006g0310a0003c0003t0006g0311others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-22740_93-22738d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-22747_93-22738d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.93-22748_93-22738d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAAAAAAA others(7): Show |
C | 32 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.93-22751_93-22738d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131767427
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0009a0001c0001t0001g0200a0001c0001t0001g0238 | 3 | HG00438.hp2 NA18979.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.93-22752_93-22738d others(17): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | ||||||
| chr5:131768033
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-23343C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768033 | ||||||
| chr5:131768465
|
GT | G | 70 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0170others(67): Show | 70 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.93-23776delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768465 | ||||||
| chr5:131768465
|
GTT | G | 139 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(136): Show | 139 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.93-23777_93-23776d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768465 | ||||||
| chr5:131768480
|
T | A | 1 | a0001c0013t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.93-23790A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768480 | ||||||
| chr5:131768493
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.93-23803T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768493 | ||||||
| chr5:131768566
|
T | G | 16 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(13): Show | 16 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.93-23876A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768566 | ||||||
| chr5:131768581
|
G | A | 1 | a0002c0002t0018g0284 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.93-23891C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768581 | ||||||
| chr5:131768707
|
G | A | 2 | a0001c0001t0009g0018a0001c0001t0009g0046 | 2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.93-24017C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768707 | ||||||
| chr5:131768712
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-24022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768712 | ||||||
| chr5:131768723
|
C | T | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-24033G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768723 | ||||||
| chr5:131768800
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.93-24110T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768800 | ||||||
| chr5:131769155
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-24465C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769155 | ||||||
| chr5:131769489
|
C | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-24799G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769489 | ||||||
| chr5:131769536
|
G | T | 1 | a0006c0010t0001g0291 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.93-24846C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769536 | ||||||
| chr5:131769655
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.93-24965C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769655 | ||||||
| chr5:131769778
|
TGAA | T | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-25091_93-25089d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769778 | ||||||
| chr5:131769779
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-25089C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769779 | ||||||
| chr5:131769808
|
T | G | 1 | a0003c0003t0006g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.93-25118A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769808 | ||||||
| chr5:131769826
|
C | T | 1 | a0001c0001t0008g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.93-25136G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769826 | ||||||
| chr5:131769843
|
A | C | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-25153T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769843 | ||||||
| chr5:131769989
|
C | T | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.93-25299G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769989 | ||||||
| chr5:131770211
|
G | A | 1 | a0002c0002t0005g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.93-25521C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770211 | ||||||
| chr5:131770259
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-25569C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770259 | ||||||
| chr5:131770458
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0175others(17): Show | 20 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.93-25768G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770458 | ||||||
| chr5:131770756
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0225 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.93-26066G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770756 | ||||||
| chr5:131770874
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.92+25956A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770874 | ||||||
| chr5:131770917
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92+25913T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770917 | ||||||
| chr5:131771069
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+25761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771069 | ||||||
| chr5:131771078
|
T | C | 2 | a0001c0001t0005g0115a0001c0001t0005g0154 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.92+25752A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771078 | ||||||
| chr5:131771303
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+25527G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771303 | ||||||
| chr5:131771357
|
C | A | 1 | a0003c0003t0006g0312 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.92+25473G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771357 | ||||||
| chr5:131771434
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+25396A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771434 | ||||||
| chr5:131771688
|
T | G | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.92+25142A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771688 | ||||||
| chr5:131771689
|
C | T | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.92+25141G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771689 | ||||||
| chr5:131771693
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+25137C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771693 | ||||||
| chr5:131771808
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.92+25022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771808 | ||||||
| chr5:131771999
|
G | A | 45 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(42): Show | 45 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.92+24831C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771999 | ||||||
| chr5:131772000
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+24830C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772000 | ||||||
| chr5:131772009
|
C | A | 1 | a0001c0008t0002g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.92+24821G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772009 | ||||||
| chr5:131772255
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+24575T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772255 | ||||||
| chr5:131772382
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+24448G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772382 | ||||||
| chr5:131772420
|
CA | C | 16 | a0001c0001t0002g0096a0001c0001t0002g0112a0001c0001t0002g0164others(13): Show | 16 | HG01168.hp2 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.92+24409delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | ||||||
| chr5:131772420
|
CAA | C | 20 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0001g0294others(17): Show | 20 | HG01081.hp1 HG01175.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+24408_92+24409d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | ||||||
| chr5:131772420
|
CAAA | C | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(152): Show | 155 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.92+24407_92+24409d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | ||||||
| chr5:131772420
|
CAAAA | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.92+24406_92+24409d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | ||||||
| chr5:131772603
|
C | T | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+24227G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772603 | ||||||
| chr5:131772726
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.92+24104A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772726 | ||||||
| chr5:131772772
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.92+24058G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772772 | ||||||
| chr5:131772837
|
A | G | 4 | a0002c0002t0002g0006a0002c0002t0002g0146a0002c0002t0002g0147others(1): Show | 4 | HG00733.hp2 HG01256.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+23993T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772837 | ||||||
| chr5:131772921
|
T | C | 1 | a0001c0001t0008g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92+23909A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772921 | ||||||
| chr5:131773097
|
T | C | 1 | a0001c0001t0005g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.92+23733A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773097 | ||||||
| chr5:131773156
|
G | T | 32 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+23674C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773156 | ||||||
| chr5:131773157
|
C | T | 32 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+23673G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773157 | ||||||
| chr5:131773245
|
T | C | 2 | a0001c0001t0005g0049a0002c0002t0004g0143 | 2 | NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.92+23585A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773245 | ||||||
| chr5:131773274
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+23556C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773274 | ||||||
| chr5:131773493
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+23337C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773493 | ||||||
| chr5:131773548
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.92+23282G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773548 | ||||||
| chr5:131773660
|
C | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+23170G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773660 | ||||||
| chr5:131773747
|
A | G | 1 | a0002c0006t0004g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92+23083T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773747 | ||||||
| chr5:131773852
|
G | T | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+22978C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773852 | ||||||
| chr5:131774099
|
T | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+22731A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774099 | ||||||
| chr5:131774395
|
C | T | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92+22435G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774395 | ||||||
| chr5:131774398
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92+22432A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774398 | ||||||
| chr5:131774432
|
C | A | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.92+22398G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774432 | ||||||
| chr5:131774580
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.92+22250C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774580 | ||||||
| chr5:131774710
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92+22120A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774710 | ||||||
| chr5:131774887
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.92+21943T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774887 | ||||||
| chr5:131775088
|
A | G | 1 | a0006c0010t0001g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.92+21742T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775088 | ||||||
| chr5:131775165
|
A | G | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+21665T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775165 | ||||||
| chr5:131775463
|
C | CAACT | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+21366_92+21367i others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775463 | ||||||
| chr5:131775528
|
C | CT | 16 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(13): Show | 16 | HG02615.hp1 HG03041.hp1 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.92+21301dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775528 | ||||||
| chr5:131775528
|
CT | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0175a0001c0001t0001g0186others(20): Show | 23 | HG01070.hp2 HG01167.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.92+21301delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775528 | ||||||
| chr5:131775621
|
G | A | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92+21209C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775621 | ||||||
| chr5:131775667
|
G | A | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+21163C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775667 | ||||||
| chr5:131775684
|
C | T | 143 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.92+21146G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775684 | ||||||
| chr5:131775712
|
G | A | 47 | a0001c0001t0001g0063a0001c0001t0001g0302a0001c0001t0003g0019others(44): Show | 47 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.92+21118C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775712 | ||||||
| chr5:131775775
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+21055C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775775 | ||||||
| chr5:131775970
|
T | G | 1 | a0001c0001t0007g0263 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.92+20860A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775970 | ||||||
| chr5:131776260
|
G | T | 1 | a0002c0002t0004g0119 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.92+20570C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776260 | ||||||
| chr5:131776417
|
G | A | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.92+20413C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776417 | ||||||
| chr5:131776429
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.92+20401A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776429 | ||||||
| chr5:131776445
|
A | G | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+20385T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776445 | ||||||
| chr5:131776516
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+20314C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776516 | ||||||
| chr5:131776550
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92+20280G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776550 | ||||||
| chr5:131776686
|
T | A | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92+20144A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776686 | ||||||
| chr5:131776934
|
C | T | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+19896G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776934 | ||||||
| chr5:131777137
|
CAT | C | 6 | a0003c0003t0006g0310a0003c0003t0006g0313a0003c0003t0006g0314others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+19691_92+19692d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777137 | ||||||
| chr5:131777227
|
C | A | 2 | a0001c0001t0001g0063a0001c0017t0001g0062 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.92+19603G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777227 | ||||||
| chr5:131777227
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+19603G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777227 | ||||||
| chr5:131777251
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0196 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.92+19579A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777251 | ||||||
| chr5:131777402
|
G | A | 6 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+19428C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777402 | ||||||
| chr5:131777637
|
A | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+19193T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777637 | ||||||
| chr5:131778036
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+18794T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778036 | ||||||
| chr5:131778047
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0005g0080 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.92+18783C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778047 | ||||||
| chr5:131778121
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.92+18709C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778121 | ||||||
| chr5:131778137
|
C | T | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.92+18693G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778137 | ||||||
| chr5:131778257
|
C | G | 1 | a0001c0001t0002g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.92+18573G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778257 | ||||||
| chr5:131778402
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+18428A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778402 | ||||||
| chr5:131778472
|
C | T | 1 | a0001c0001t0005g0111 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.92+18358G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778472 | ||||||
| chr5:131778473
|
G | C | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 185 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.92+18357C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778473 | ||||||
| chr5:131778514
|
G | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+18316C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778514 | ||||||
| chr5:131778688
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92+18142G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778688 | ||||||
| chr5:131778835
|
T | G | 1 | a0004c0007t0001g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92+17995A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778835 | ||||||
| chr5:131778840
|
T | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+17990A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778840 | ||||||
| chr5:131778848
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.92+17982C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778848 | ||||||
| chr5:131778868
|
C | T | 1 | a0001c0017t0001g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92+17962G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778868 | ||||||
| chr5:131778890
|
G | A | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+17940C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778890 | ||||||
| chr5:131778913
|
G | A | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+17917C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778913 | ||||||
| chr5:131778964
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.92+17866C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778964 | ||||||
| chr5:131779069
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+17761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779069 | ||||||
| chr5:131779135
|
T | G | 1 | a0001c0001t0002g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.92+17695A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779135 | ||||||
| chr5:131779147
|
TA | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0179a0001c0001t0001g0188others(6): Show | 9 | HG01070.hp1 HG01943.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+17682delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779147 | ||||||
| chr5:131779194
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+17636C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779194 | ||||||
| chr5:131779213
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+17617A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779213 | ||||||
| chr5:131779286
|
A | T | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.92+17544T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779286 | ||||||
| chr5:131779372
|
G | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+17458C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779372 | ||||||
| chr5:131779382
|
T | G | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.92+17448A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779382 | ||||||
| chr5:131779504
|
C | A | 1 | a0003c0003t0006g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92+17326G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779504 | ||||||
| chr5:131779516
|
T | TA | 76 | a0001c0001t0002g0081a0001c0001t0002g0112a0001c0001t0002g0122others(73): Show | 77 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.92+17313dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779516 | ||||||
| chr5:131779531
|
T | A | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+17299A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779531 | ||||||
| chr5:131779556
|
C | T | 1 | a0001c0001t0003g0020 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+17274G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779556 | ||||||
| chr5:131779580
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.92+17250G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779580 | ||||||
| chr5:131779655
|
T | C | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+17175A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779655 | ||||||
| chr5:131779687
|
C | CA | 6 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+17142dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779687 | ||||||
| chr5:131779687
|
CA | C | 11 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0230others(8): Show | 11 | HG01169.hp2 HG01257.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+17142delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779687 | ||||||
| chr5:131779781
|
T | C | 4 | a0002c0002t0002g0123a0002c0002t0002g0161a0002c0002t0002g0272others(1): Show | 4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+17049A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779781 | ||||||
| chr5:131780046
|
T | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0225a0002c0002t0019g0058 | 3 | HG02486.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.92+16784A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780046 | ||||||
| chr5:131780276
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92+16554A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780276 | ||||||
| chr5:131780362
|
A | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.92+16468T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780362 | ||||||
| chr5:131780389
|
C | A | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 124 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.92+16441G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780389 | ||||||
| chr5:131780538
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0264 | 2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.92+16292A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780538 | ||||||
| chr5:131780631
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.92+16199C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780631 | ||||||
| chr5:131780688
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+16142C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780688 | ||||||
| chr5:131781128
|
G | A | 1 | a0002c0002t0002g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.92+15702C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781128 | ||||||
| chr5:131781206
|
T | C | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+15624A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781206 | ||||||
| chr5:131781580
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+15250T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781580 | ||||||
| chr5:131781833
|
A | C | 2 | a0001c0001t0002g0096a0001c0001t0005g0276 | 2 | HG01099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.92+14997T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781833 | ||||||
| chr5:131781851
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.92+14979C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781851 | ||||||
| chr5:131781899
|
T | C | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+14931A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781899 | ||||||
| chr5:131782167
|
T | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+14663A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782167 | ||||||
| chr5:131782225
|
C | A | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+14605G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782225 | ||||||
| chr5:131782319
|
C | T | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+14511G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782319 | ||||||
| chr5:131782375
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92+14455G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782375 | ||||||
| chr5:131782407
|
C | A | 190 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(187): Show | 190 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.92+14423G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782407 | ||||||
| chr5:131782472
|
C | G | 203 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+14358G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782472 | ||||||
| chr5:131782650
|
T | C | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+14180A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782650 | ||||||
| chr5:131782799
|
T | C | 42 | a0001c0001t0001g0063a0001c0001t0001g0302a0001c0001t0003g0019others(39): Show | 42 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.92+14031A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782799 | ||||||
| chr5:131782954
|
C | T | 1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+13876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782954 | ||||||
| chr5:131783000
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92+13830T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783000 | ||||||
| chr5:131783045
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92+13785C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783045 | ||||||
| chr5:131783131
|
T | C | 13 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(10): Show | 13 | NA18945.hp1 NA18947.hp2 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.92+13699A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783131 | ||||||
| chr5:131783250
|
T | C | 143 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.92+13580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783250 | ||||||
| chr5:131783426
|
A | G | 1 | a0002c0002t0005g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92+13404T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783426 | ||||||
| chr5:131783453
|
C | CA | 6 | a0001c0001t0001g0300a0001c0001t0002g0081a0001c0001t0005g0080others(3): Show | 6 | HG01081.hp1 HG02630.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+13376dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783453 | ||||||
| chr5:131783453
|
C | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+13377G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783453 | ||||||
| chr5:131783494
|
A | G | 32 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+13336T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783494 | ||||||
| chr5:131783707
|
T | G | 5 | a0001c0001t0009g0018a0001c0001t0009g0044a0001c0001t0009g0045others(2): Show | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+13123A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783707 | ||||||
| chr5:131784008
|
C | CA | 142 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.92+12821dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784008 | ||||||
| chr5:131784141
|
G | T | 1 | a0001c0001t0002g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.92+12689C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784141 | ||||||
| chr5:131784244
|
G | A | 1 | a0002c0002t0002g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.92+12586C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784244 | ||||||
| chr5:131784255
|
T | C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+12575A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784255 | ||||||
| chr5:131784517
|
T | C | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+12313A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784517 | ||||||
| chr5:131784609
|
C | G | 1 | a0002c0006t0004g0125 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92+12221G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784609 | ||||||
| chr5:131784614
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.92+12216T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784614 | ||||||
| chr5:131784645
|
A | AC | 17 | a0001c0001t0002g0081a0001c0001t0002g0083a0001c0001t0002g0084others(14): Show | 17 | HG01081.hp1 HG02486.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.92+12184dupG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784645 | ||||||
| chr5:131784874
|
A | C | 1 | a0001c0001t0002g0053 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.92+11956T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784874 | ||||||
| chr5:131784895
|
G | A | 2 | a0001c0005t0007g0065a0001c0005t0007g0070 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.92+11935C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784895 | ||||||
| chr5:131784932
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+11898G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784932 | ||||||
| chr5:131785001
|
TATATGAC others(21): Show |
T | 1 | a0001c0001t0001g0226 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92+11801_92+11828d others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785001 | ||||||
| chr5:131785008
|
CTATATAT others(65): Show |
C | 5 | a0003c0003t0006g0310a0003c0003t0006g0314a0003c0003t0006g0315others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+11750_92+11821d others(74): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785008 | ||||||
| chr5:131785009
|
TATATATA others(13): Show |
T | 9 | a0001c0001t0001g0057a0001c0001t0001g0198a0001c0001t0007g0229others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+11801_92+11820d others(22): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | ||||||
| chr5:131785009
|
TATATATA others(63): Show |
T | 3 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068 | 3 | HG02809.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92+11751_92+11820d others(72): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | ||||||
| chr5:131785009
|
TATATATA others(130): Show |
T | 3 | a0001c0001t0001g0063a0001c0017t0001g0062a0008c0016t0001g0190 | 3 | HG02559.hp2 HG02809.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.92+11684_92+11820d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | ||||||
| chr5:131785011
|
TATATATG others(11): Show |
T | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.92+11801_92+11818d others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | ||||||
| chr5:131785011
|
TATATATG others(95): Show |
T | 20 | a0001c0001t0001g0179a0001c0001t0001g0188a0001c0001t0001g0191others(17): Show | 20 | HG00642.hp1 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+11717_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | ||||||
| chr5:131785011
|
TATATATG others(128): Show |
T | 11 | a0001c0001t0001g0055a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+11684_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | ||||||
| chr5:131785011
|
TATATATG others(160): Show |
T | 2 | a0001c0001t0001g0008a0001c0001t0001g0175 | 2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.92+11652_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | ||||||
| chr5:131785028
|
A | ACTATATA others(3): Show |
1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11801_92+11802i others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785028 | ||||||
| chr5:131785028
|
A | ACTATATA others(5): Show |
1 | a0003c0003t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+11801_92+11802i others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785028 | ||||||
| chr5:131785029
|
CATATATA others(109): Show |
C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+11685_92+11800d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785029 | ||||||
| chr5:131785038
|
G | C | 1 | a0002c0002t0004g0145 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.92+11792C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785038 | ||||||
| chr5:131785049
|
CTATATAT others(24): Show |
C | 9 | a0001c0001t0001g0266a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+11750_92+11780d others(33): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785049 | ||||||
| chr5:131785049
|
CTATATAT others(47): Show |
C | 1 | a0003c0003t0006g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.92+11727_92+11780d others(56): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785049 | ||||||
| chr5:131785050
|
TATATATA others(56): Show |
T | 24 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0302others(21): Show | 24 | HG00639.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.92+11717_92+11779d others(65): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785050 | ||||||
| chr5:131785050
|
TATATATA others(89): Show |
T | 117 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 117 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.92+11684_92+11779d others(98): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785050 | ||||||
| chr5:131785058
|
TCATATAT others(14): Show |
T | 4 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0316others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+11751_92+11771d others(23): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785058 | ||||||
| chr5:131785059
|
C | G | 2 | a0001c0001t0001g0197a0001c0015t0001g0326 | 2 | HG02602.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.92+11771G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785059 | ||||||
| chr5:131785059
|
CATATATA others(15): Show |
C | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11749_92+11770d others(24): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785059 | ||||||
| chr5:131785068
|
GATATATA others(35): Show |
G | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11720_92+11761d others(44): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785068 | ||||||
| chr5:131785069
|
ATATATAT others(68): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+11686_92+11760d others(77): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785069 | ||||||
| chr5:131785079
|
CAT | C | 5 | a0001c0001t0002g0122a0001c0001t0002g0164a0001c0001t0005g0076others(2): Show | 5 | HG01081.hp1 HG02735.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+11749_92+11750d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785079 | ||||||
| chr5:131785081
|
T | TATATATA others(25): Show |
2 | a0002c0002t0004g0162a0007c0012t0005g0117 | 2 | NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.92+11717_92+11748d others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785081 | ||||||
| chr5:131785081
|
T | TC | 4 | a0003c0003t0006g0311a0003c0003t0006g0312a0003c0003t0006g0316others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+11748_92+11749i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785081 | ||||||
| chr5:131785096
|
T | C | 2 | a0002c0002t0002g0156a0002c0002t0002g0271 | 2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.92+11734A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785096 | ||||||
| chr5:131785102
|
TATATATA others(4): Show |
T | 3 | a0001c0005t0001g0066a0001c0005t0001g0067a0001c0005t0001g0068 | 3 | HG02809.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92+11717_92+11727d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785102 | ||||||
| chr5:131785109
|
ATATCATA others(28): Show |
A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+11686_92+11720d others(37): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785109 | ||||||
| chr5:131785111
|
A | ATCATATA others(26): Show |
4 | a0002c0002t0002g0123a0002c0002t0002g0161a0002c0002t0002g0272others(1): Show | 4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+11686_92+11718d others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | ||||||
| chr5:131785111
|
A | ATCATATA others(58): Show |
1 | a0002c0002t0002g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.92+11718_92+11719i others(67): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | ||||||
| chr5:131785111
|
ATCATATA others(26): Show |
A | 5 | a0001c0001t0002g0081a0001c0001t0002g0274a0001c0001t0005g0078others(2): Show | 5 | HG02015.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+11686_92+11718d others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | ||||||
| chr5:131785112
|
T | C | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11718A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785112 | ||||||
| chr5:131785113
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11717G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785113 | ||||||
| chr5:131785134
|
TATATATA others(5): Show |
T | 5 | a0001c0001t0001g0179a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 5 | HG00544.hp1 HG01070.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+11684_92+11695d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785134 | ||||||
| chr5:131785143
|
AG | A | 57 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0302others(54): Show | 57 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.92+11686delC | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785143 | ||||||
| chr5:131785144
|
G | GTCATATA others(25): Show |
2 | a0002c0002t0004g0119a0002c0002t0004g0160 | 2 | NA18942.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.92+11654_92+11685d others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785144 | ||||||
| chr5:131785145
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0002g0164 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.92+11685A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785145 | ||||||
| chr5:131785146
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0322 | 2 | HG02602.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.92+11684G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785146 | ||||||
| chr5:131785155
|
G | C | 1 | a0001c0001t0002g0280 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92+11675C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785155 | ||||||
| chr5:131785167
|
TATATATA others(4): Show |
T | 11 | a0001c0001t0001g0055a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+11652_92+11662d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785167 | ||||||
| chr5:131785176
|
A | AG | 33 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(30): Show | 33 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.92+11653_92+11654i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785176 | ||||||
| chr5:131785176
|
A | G | 3 | a0002c0002t0002g0006a0002c0002t0002g0146a0002c0002t0002g0147 | 3 | HG00733.hp2 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.92+11654T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785176 | ||||||
| chr5:131785327
|
G | A | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11503C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785327 | ||||||
| chr5:131785346
|
G | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+11484C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785346 | ||||||
| chr5:131785427
|
C | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+11403G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785427 | ||||||
| chr5:131785472
|
T | C | 4 | a0002c0002t0002g0006a0002c0002t0002g0146a0002c0002t0002g0147others(1): Show | 4 | HG00733.hp2 HG01256.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+11358A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785472 | ||||||
| chr5:131785550
|
CA | C | 252 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(249): Show | 253 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.92+11279delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785550 | ||||||
| chr5:131785733
|
A | G | 1 | a0001c0005t0007g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+11097T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785733 | ||||||
| chr5:131785950
|
C | T | 1 | a0001c0001t0005g0078 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.92+10880G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785950 | ||||||
| chr5:131785954
|
C | T | 3 | a0004c0007t0001g0174a0004c0007t0001g0181a0004c0007t0001g0182 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+10876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785954 | ||||||
| chr5:131786072
|
T | G | 1 | a0001c0001t0001g0267 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.92+10758A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786072 | ||||||
| chr5:131786205
|
T | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+10625A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786205 | ||||||
| chr5:131786295
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.92+10535G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786295 | ||||||
| chr5:131786310
|
C | A | 8 | a0001c0001t0001g0302a0001c0001t0003g0303a0001c0001t0003g0304others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+10520G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786310 | ||||||
| chr5:131786411
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.92+10419C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786411 | ||||||
| chr5:131786790
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92+10040G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786790 | ||||||
| chr5:131786810
|
A | C | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+10020T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786810 | ||||||
| chr5:131787230
|
GC | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0227a0001c0001t0023g0228 | 3 | HG00609.hp2 NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.92+9599delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787230 | ||||||
| chr5:131787581
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.92+9249A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787581 | ||||||
| chr5:131787702
|
T | C | 38 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(35): Show | 38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.92+9128A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787702 | ||||||
| chr5:131787894
|
C | T | 1 | a0008c0016t0001g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.92+8936G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787894 | ||||||
| chr5:131787899
|
T | C | 2 | a0004c0007t0001g0181a0004c0007t0001g0182 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+8931A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787899 | ||||||
| chr5:131788019
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0074 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+8811G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788019 | ||||||
| chr5:131788049
|
A | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+8781T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788049 | ||||||
| chr5:131788072
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+8758G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788072 | ||||||
| chr5:131788079
|
T | A | 1 | a0002c0002t0004g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.92+8751A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788079 | ||||||
| chr5:131788296
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+8534T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788296 | ||||||
| chr5:131788407
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+8423C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788407 | ||||||
| chr5:131788557
|
T | G | 32 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+8273A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788557 | ||||||
| chr5:131788694
|
C | CA | 13 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0163others(10): Show | 13 | HG00544.hp2 HG02040.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+8135dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788694 | ||||||
| chr5:131788694
|
CA | C | 56 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(53): Show | 56 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.92+8135delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788694 | ||||||
| chr5:131788847
|
A | G | 1 | a0002c0002t0002g0281 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92+7983T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788847 | ||||||
| chr5:131788945
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.92+7885C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788945 | ||||||
| chr5:131788972
|
T | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+7858A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788972 | ||||||
| chr5:131789260
|
G | A | 2 | a0002c0002t0002g0158a0002c0002t0002g0159 | 2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.92+7570C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789260 | ||||||
| chr5:131789387
|
T | A | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.92+7443A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789387 | ||||||
| chr5:131789588
|
C | T | 6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+7242G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789588 | ||||||
| chr5:131789591
|
C | T | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+7239G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789591 | ||||||
| chr5:131789716
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.92+7114A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789716 | ||||||
| chr5:131790066
|
C | T | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+6764G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790066 | ||||||
| chr5:131790185
|
A | G | 1 | a0002c0002t0019g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+6645T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790185 | ||||||
| chr5:131790295
|
G | A | 55 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(52): Show | 55 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.92+6535C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790295 | ||||||
| chr5:131790434
|
G | A | 2 | a0005c0009t0014g0050a0005c0009t0015g0051 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+6396C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790434 | ||||||
| chr5:131790478
|
C | CA | 65 | a0001c0001t0001g0322a0001c0001t0002g0053a0001c0001t0002g0149others(62): Show | 66 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.92+6351dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
C | CAA | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.92+6350_92+6351dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
C | CAAA | 67 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(64): Show | 67 | HG00408.hp2 HG00639.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.92+6349_92+6351dup others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
C | CAAAA | 56 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0227others(53): Show | 56 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.92+6348_92+6351dup others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
C | CAAAAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG01978.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+6347_92+6351dup others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
C | CAAAAAAA others(3): Show |
1 | a0001c0013t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92+6342_92+6351dup others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790478
|
CAAAAAAA others(1): Show |
C | 31 | a0001c0001t0001g0302a0001c0001t0003g0019a0001c0001t0003g0020others(28): Show | 31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.92+6344_92+6351del others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | ||||||
| chr5:131790639
|
GAAGA | G | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0074 | 3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+6187_92+6190del others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790639 | ||||||
| chr5:131791334
|
C | T | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+5496G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791334 | ||||||
| chr5:131791594
|
A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+5236T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791594 | ||||||
| chr5:131791608
|
A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+5222T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791608 | ||||||
| chr5:131791857
|
T | A | 12 | a0001c0001t0001g0063a0001c0017t0001g0062a0003c0003t0006g0310others(9): Show | 12 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.92+4973A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791857 | ||||||
| chr5:131791878
|
GA | G | 141 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(138): Show | 141 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.92+4951delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791878 | ||||||
| chr5:131791923
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.92+4907A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791923 | ||||||
| chr5:131791940
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0289 | 3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.92+4890G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791940 | ||||||
| chr5:131791981
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+4849G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791981 | ||||||
| chr5:131792160
|
C | CT | 54 | a0001c0001t0001g0063a0001c0001t0001g0169a0001c0001t0001g0170others(51): Show | 54 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.92+4669dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792160 | ||||||
| chr5:131792213
|
T | A | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+4617A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792213 | ||||||
| chr5:131792213
|
T | C | 1 | a0001c0001t0002g0165 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.92+4617A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792213 | ||||||
| chr5:131792222
|
G | A | 1 | a0003c0003t0006g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92+4608C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792222 | ||||||
| chr5:131792307
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92+4523G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792307 | ||||||
| chr5:131792345
|
G | C | 1 | a0001c0001t0005g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92+4485C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792345 | ||||||
| chr5:131792658
|
G | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+4172C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792658 | ||||||
| chr5:131792722
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+4108T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792722 | ||||||
| chr5:131792849
|
C | G | 1 | a0001c0001t0002g0274 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92+3981G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792849 | ||||||
| chr5:131792857
|
C | CA | 146 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.92+3972dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792857 | ||||||
| chr5:131793083
|
T | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+3747A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793083 | ||||||
| chr5:131793092
|
G | A | 1 | a0002c0002t0002g0272 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92+3738C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793092 | ||||||
| chr5:131793122
|
C | G | 9 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0006g0069others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+3708G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793122 | ||||||
| chr5:131793496
|
A | G | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+3334T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793496 | ||||||
| chr5:131793499
|
A | G | 3 | a0001c0001t0001g0063a0001c0015t0001g0326a0001c0017t0001g0062 | 3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92+3331T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793499 | ||||||
| chr5:131793778
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92+3052A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793778 | ||||||
| chr5:131794174
|
A | G | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.92+2656T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794174 | ||||||
| chr5:131794229
|
T | TA | 29 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0292others(26): Show | 30 | HG01099.hp1 HG01109.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+2600dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | ||||||
| chr5:131794229
|
TA | T | 52 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(49): Show | 52 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.92+2600delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | ||||||
| chr5:131794229
|
TAA | T | 10 | a0001c0001t0009g0018a0003c0003t0006g0310a0003c0003t0006g0311others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+2599_92+2600del others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | ||||||
| chr5:131794450
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92+2380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794450 | ||||||
| chr5:131794603
|
G | A | 1 | a0001c0001t0008g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+2227C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794603 | ||||||
| chr5:131794673
|
C | A | 8 | a0001c0001t0001g0302a0001c0001t0003g0303a0001c0001t0003g0304others(5): Show | 8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+2157G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794673 | ||||||
| chr5:131794815
|
A | C | 1 | a0009c0018t0007g0017 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.92+2015T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794815 | ||||||
| chr5:131795230
|
A | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.92+1600T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795230 | ||||||
| chr5:131795340
|
G | A | 325 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 327 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(324): Show |
intron_variant | MODIFIER | c.92+1490C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795340 | ||||||
| chr5:131795486
|
T | A | 10 | a0003c0003t0006g0310a0003c0003t0006g0311a0003c0003t0006g0312others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+1344A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795486 | ||||||
| chr5:131795538
|
T | C | 1 | a0001c0001t0016g0320 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.92+1292A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795538 | ||||||
| chr5:131796097
|
A | G | 325 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 327 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(324): Show |
intron_variant | MODIFIER | c.92+733T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796097 | ||||||
| chr5:131796114
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+716A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796114 | ||||||
| chr5:131796309
|
G | C | 2 | a0001c0001t0008g0323a0001c0001t0008g0324 | 2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+521C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796309 | ||||||
| chr5:131796453
|
C | T | 1 | a0001c0001t0010g0013 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.92+377G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796453 | ||||||
| chr5:131796606
|
G | C | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92+224C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796606 | ||||||
| chr5:131796632
|
G | A | 1 | a0001c0015t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+198C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796632 | ||||||
| chr5:131796807
|
A | AC | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG00438.hp1 HG02738.hp1 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.92+22dupG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796807 |