Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57600 |
| ensemblid | ENSG00000052795.13 |
| hgncid | 29280 |
| symbol | FNIP2 |
| name | folliculin interacting protein 2 |
| refseq_nuc | NM_020840.3 |
| refseq_prot | NP_065891.1 |
| ensembl_nuc | ENST00000264433.11 |
| ensembl_prot | ENSP00000264433.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 158769026 |
| end | 158908050 |
| strand | + |
| ver | v1.2 |
| region | chr4:158769026-158908050 |
| region5000 | chr4:158764026-158913050 |
| regionname0 | FNIP2_chr4_158769026_158908050 |
| regionname5000 | FNIP2_chr4_158764026_158913050 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1114 | 195 | 62 | 40 | 58 | 7 | 26 | 39 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002 | 0/0 | 1114 | 37 | 9 | 3 | 20 | 1 | 4 | 15 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0003 | 0/0 | 1114 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0004 | 0/0 | 1114 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0005 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0006 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0007 | 0/0 | 1114 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0008 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0009 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0010 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0011 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3345 | 165 | 41 | 40 | 55 | 7 | 20 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0002 | 0/0 | 3345 | 36 | 8 | 3 | 20 | 1 | 4 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0003 | 0/0 | 3345 | 16 | 12 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0004 | 0/0 | 3345 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0005 | 0/0 | 3345 | 5 | 0 | 0 | 0 | 0 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0006 | 0/0 | 3345 | 5 | 0 | 4 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0007 | 0/0 | 3345 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0008 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0009 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0010 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0011 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0012 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0013 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0014 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0015 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0016 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0017 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| c0018 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3693 | 114 | 29 | 24 | 40 | 4 | 16 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0002 | 0/0 | 3693 | 48 | 7 | 17 | 9 | 5 | 10 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0003 | 0/0 | 3693 | 35 | 6 | 3 | 20 | 1 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0004 | 0/0 | 3693 | 17 | 13 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0005 | 0/0 | 3692 | 9 | 8 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0006 | 1/0 | 3694 | 5 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0007 | 0/0 | 3697 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0008 | 0/0 | 3694 | 4 | 2 | 1 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0009 | 0/0 | 3694 | 3 | 1 | 0 | 2 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0010 | 0/0 | 3693 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0011 | 0/0 | 3693 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0012 | 0/0 | 3693 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0013 | 0/0 | 3693 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0014 | 0/0 | 3693 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0015 | 0/0 | 3693 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0016 | 0/0 | 3694 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0017 | 0/0 | 3694 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0018 | 0/0 | 3693 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0019 | 0/0 | 3693 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| t0020 | 0/0 | 3694 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3345 | 165 | 41 | 40 | 55 | 7 | 20 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0003 | 0/0 | 3345 | 16 | 12 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0005 | 0/0 | 3345 | 5 | 0 | 0 | 0 | 0 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0007 | 0/0 | 3345 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0008 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0009 | 0/0 | 3345 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0014 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0002 | 0/0 | 3345 | 36 | 8 | 3 | 20 | 1 | 4 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0017 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0003c0004 | 0/0 | 3345 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0004c0006 | 0/0 | 3345 | 5 | 0 | 4 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0005c0018 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0006c0010 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0007c0011 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0008c0012 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0009c0016 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0010c0015 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0011c0013 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7037 | 103 | 19 | 24 | 40 | 4 | 15 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0002 | 0/0 | 7037 | 34 | 4 | 13 | 9 | 3 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0003 | 0/0 | 7037 | 2 | 1 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0004 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0005 | 0/0 | 7036 | 8 | 8 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0006 | 1/0 | 7038 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0007 | 0/0 | 7041 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0008 | 0/0 | 7038 | 3 | 1 | 1 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0009 | 0/0 | 7038 | 3 | 1 | 0 | 2 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0011 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0012 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0014 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0015 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0018 | 0/0 | 7037 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0001t0019 | 0/0 | 7037 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0003t0004 | 0/0 | 7037 | 13 | 9 | 0 | 3 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0003t0013 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0003t0017 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0005t0002 | 0/0 | 7037 | 5 | 0 | 0 | 0 | 0 | 5 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0007t0006 | 0/0 | 7038 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0008t0010 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0009t0002 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0001c0014t0020 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0002t0003 | 0/0 | 7037 | 31 | 4 | 3 | 19 | 1 | 4 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0002t0004 | 0/0 | 7037 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0002t0007 | 0/0 | 7041 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0002t0016 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0002c0017t0003 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0003c0004t0001 | 0/0 | 7037 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0004c0006t0002 | 0/0 | 7037 | 5 | 0 | 4 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0005c0018t0003 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0006c0010t0001 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0007c0011t0005 | 0/0 | 7036 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0008c0012t0002 | 0/0 | 7037 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0009c0016t0002 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0010c0015t0004 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| a0011c0013t0008 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | copy fasta | chr4 | 158764026 | 158913050 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0006g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0014g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0018g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0001t0019g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0003t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0007t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0008t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0008t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0009t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0009t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0001c0014t0020g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0002t0016g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0002c0017t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0003c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0004c0006t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0005c0018t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0006c0010t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0007c0011t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0008c0012t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0009c0016t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0010c0015t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| a0011c0013t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0198 | EUR | FIN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | FIN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0179 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0174 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0173 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00597 | hp2 | a0001 | c0001 | t0009 | g0244 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00609 | hp2 | a0001 | c0003 | t0004 | g0134 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0166 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01169 | hp2 | a0002 | c0002 | t0003 | g0201 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01257 | hp2 | a0004 | c0006 | t0002 | g0246 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01258 | hp1 | a0004 | c0006 | t0002 | g0248 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01258 | hp2 | a0001 | c0001 | t0018 | g0124 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01261 | hp1 | a0004 | c0006 | t0002 | g0214 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01884 | hp2 | a0001 | c0009 | t0002 | g0234 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0089 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01934 | hp2 | a0001 | c0001 | t0019 | g0111 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0189 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01975 | hp2 | a0004 | c0006 | t0002 | g0224 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0120 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG01981 | hp2 | a0007 | c0011 | t0005 | g0004 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0029 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02055 | hp2 | a0001 | c0007 | t0006 | g0163 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02080 | hp2 | a0002 | c0002 | t0016 | g0177 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0182 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0126 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0088 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02145 | hp2 | a0001 | c0007 | t0006 | g0165 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02258 | hp2 | a0002 | c0017 | t0003 | g0030 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0037 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02572 | hp1 | a0001 | c0003 | t0017 | g0017 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02572 | hp2 | a0003 | c0004 | t0001 | g0053 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02615 | hp2 | a0010 | c0015 | t0004 | g0013 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0055 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0026 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02683 | hp1 | a0001 | c0003 | t0004 | g0024 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0054 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0185 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02735 | hp2 | a0001 | c0005 | t0002 | g0213 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02818 | hp2 | a0001 | c0009 | t0002 | g0235 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02886 | hp1 | a0001 | c0007 | t0006 | g0012 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0167 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0080 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02896 | hp1 | a0001 | c0008 | t0010 | g0034 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02897 | hp1 | a0001 | c0008 | t0010 | g0033 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0150 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02965 | hp2 | a0001 | c0003 | t0013 | g0027 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | GWD | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03195 | hp1 | a0002 | c0002 | t0007 | g0170 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03195 | hp2 | a0001 | c0003 | t0013 | g0028 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0181 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0149 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03491 | hp1 | a0001 | c0005 | t0002 | g0211 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03492 | hp1 | a0001 | c0005 | t0002 | g0215 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03516 | hp1 | a0003 | c0004 | t0001 | g0148 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03516 | hp2 | a0009 | c0016 | t0002 | g0236 | AFR | ESN | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0228 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03710 | hp2 | a0005 | c0018 | t0003 | g0183 | SAS | PJL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03942 | hp1 | a0006 | c0010 | t0001 | g0128 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03942 | hp2 | a0001 | c0005 | t0002 | g0225 | SAS | BEB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18522 | hp1 | a0011 | c0013 | t0008 | g0151 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0018 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0056 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | YRI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0142 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18989 | hp1 | a0002 | c0002 | t0003 | g0199 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0192 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0187 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19009 | hp1 | a0001 | c0003 | t0004 | g0125 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19030 | hp1 | a0001 | c0014 | t0020 | g0035 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19060 | hp1 | a0001 | c0001 | t0015 | g0097 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0178 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0231 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0180 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19087 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19087 | hp2 | a0002 | c0002 | t0003 | g0195 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19089 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ASW | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20752 | hp2 | a0008 | c0012 | t0002 | g0210 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20805 | hp2 | a0004 | c0006 | t0002 | g0247 | EUR | TSI | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0197 | SAS | GIH | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | GIH | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0057 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02486 | hp2 | a0001 | c0007 | t0006 | g0164 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02559 | hp1 | a0002 | c0002 | t0007 | g0169 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | USA | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0147 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0038 | AFR | LWK | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0003 | REF | REF | FNIP2_chr4_158764026_158913050 | FNIP2 | chr4 | 158764026 | 158913050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158859092
|
C | G | 2 | a0002a0005 | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
missense_variant | MODERATE | c.893C>G | p.Thr298Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/17 | 1080/7038 | 893/3345 | 298/1114 | chr4 | 158859092 | ||
| chr4:158859100
|
T | C | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.901T>C | p.Ser301Pro | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/17 | 1088/7038 | 901/3345 | 301/1114 | chr4 | 158859100 | ||
| chr4:158861737
|
G | T | 1 | a0004 | 5 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(2): Show |
missense_variant | MODERATE | c.1426G>T | p.Ala476Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/17 | 1613/7038 | 1426/3345 | 476/1114 | chr4 | 158861737 | ||
| chr4:158868261
|
G | C | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1625G>C | p.Gly542Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1812/7038 | 1625/3345 | 542/1114 | chr4 | 158868261 | ||
| chr4:158868666
|
T | C | 1 | a0003 | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
missense_variant | MODERATE | c.2030T>C | p.Met677Thr | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2217/7038 | 2030/3345 | 677/1114 | chr4 | 158868666 | ||
| chr4:158868858
|
G | A | 1 | a0008 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2222G>A | p.Arg741Gln | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2409/7038 | 2222/3345 | 741/1114 | chr4 | 158868858 | ||
| chr4:158868981
|
G | A | 1 | a0009 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2345G>A | p.Arg782Gln | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2532/7038 | 2345/3345 | 782/1114 | chr4 | 158868981 | ||
| chr4:158869046
|
G | A | 1 | a0011 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2410G>A | p.Asp804Asn | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2597/7038 | 2410/3345 | 804/1114 | chr4 | 158869046 | ||
| chr4:158869122
|
C | T | 1 | a0010 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.2486C>T | p.Thr829Met | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2673/7038 | 2486/3345 | 829/1114 | chr4 | 158869122 | ||
| chr4:158891507
|
G | T | 1 | a0005 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.3011G>T | p.Trp1004Leu | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/17 | 3198/7038 | 3011/3345 | 1004/1114 | chr4 | 158891507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158861342
|
A | G | 2 | a0001c0009a0009c0016 | 3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1149A>G | p.Arg383Arg | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 11/17 | 1336/7038 | 1149/3345 | 383/1114 | chr4 | 158861342 | ||
| chr4:158868112
|
C | T | 1 | a0001c0005 | 5 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
synonymous_variant | LOW | c.1476C>T | p.Tyr492Tyr | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1663/7038 | 1476/3345 | 492/1114 | chr4 | 158868112 | ||
| chr4:158868403
|
G | A | 1 | a0001c0007 | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
synonymous_variant | LOW | c.1767G>A | p.Glu589Glu | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 1954/7038 | 1767/3345 | 589/1114 | chr4 | 158868403 | ||
| chr4:158868859
|
G | C | 1 | a0002c0017 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2223G>C | p.Arg741Arg | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2410/7038 | 2223/3345 | 741/1114 | chr4 | 158868859 | ||
| chr4:158869321
|
C | T | 1 | a0001c0014 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2685C>T | p.Ser895Ser | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/17 | 2872/7038 | 2685/3345 | 895/1114 | chr4 | 158869321 | ||
| chr4:158870367
|
G | A | 1 | a0001c0003 | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
synonymous_variant | LOW | c.2847G>A | p.Ala949Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/17 | 3034/7038 | 2847/3345 | 949/1114 | chr4 | 158870367 | ||
| chr4:158904499
|
T | C | 1 | a0001c0008 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.3300T>C | p.Ala1100Ala | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 3487/7038 | 3300/3345 | 1100/1114 | chr4 | 158904499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158769188
|
C | A | 1 | a0001c0001t0014 | 1 | NA18966.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/17 | 25 | chr4 | 158769188 | |||||
| chr4:158904633
|
G | A | 1 | a0001c0001t0015 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 89 | chr4 | 158904633 | |||||
| chr4:158904924
|
G | C | 1 | a0001c0008t0010 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 380 | chr4 | 158904924 | |||||
| chr4:158904997
|
C | T | 1 | a0001c0003t0013 | 2 | HG02965.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 453 | chr4 | 158904997 | |||||
| chr4:158905227
|
T | C | 7 | a0001c0001t0002a0001c0001t0009a0001c0005t0002others(4): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*683T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 683 | chr4 | 158905227 | |||||
| chr4:158905609
|
T | G | 2 | a0001c0001t0007a0002c0002t0007 | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1065T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1065 | chr4 | 158905609 | |||||
| chr4:158905621
|
T | G | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | 246 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*1077T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1077 | chr4 | 158905621 | |||||
| chr4:158905694
|
CA | C | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 230 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1166delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1166 | INFO_REALIGN_3_PRIME | chr4 | 158905694 | ||||
| chr4:158905709
|
AAC | A | 2 | a0001c0001t0005a0007c0011t0005 | 9 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1168delCA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1167 | INFO_REALIGN_3_PRIME | chr4 | 158905709 | ||||
| chr4:158905715
|
C | CTAAT | 2 | a0001c0001t0007a0002c0002t0007 | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1173_*1176dupAATT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1177 | INFO_REALIGN_3_PRIME | chr4 | 158905715 | ||||
| chr4:158905756
|
C | T | 1 | a0001c0014t0020 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1212 | chr4 | 158905756 | |||||
| chr4:158906007
|
A | C | 1 | a0001c0001t0012 | 2 | HG01891.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1463A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1463 | chr4 | 158906007 | |||||
| chr4:158906071
|
T | G | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | 249 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1527T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1527 | chr4 | 158906071 | |||||
| chr4:158906161
|
T | C | 7 | a0001c0001t0002a0001c0001t0009a0001c0005t0002others(4): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1617T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1617 | chr4 | 158906161 | |||||
| chr4:158906501
|
C | T | 1 | a0001c0001t0011 | 2 | HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 1957 | chr4 | 158906501 | |||||
| chr4:158906655
|
C | T | 1 | a0001c0001t0019 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2111 | chr4 | 158906655 | |||||
| chr4:158906656
|
G | A | 5 | a0001c0001t0003a0002c0002t0003a0002c0002t0016others(2): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2112G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2112 | chr4 | 158906656 | |||||
| chr4:158907176
|
T | C | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(7): Show | 124 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2632T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2632 | chr4 | 158907176 | |||||
| chr4:158907537
|
C | G | 1 | a0001c0001t0018 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 17/17 | 2993 | chr4 | 158907537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158769382
|
G | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG02083.hp1 NA18955.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+63G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769382 | ||||||
| chr4:158769470
|
C | T | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+151C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769470 | ||||||
| chr4:158769488
|
C | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+169C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769488 | ||||||
| chr4:158769491
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.107+172C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769491 | ||||||
| chr4:158769554
|
A | T | 1 | a0001c0001t0002g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.107+235A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769554 | ||||||
| chr4:158769820
|
A | G | 34 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.107+501A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769820 | ||||||
| chr4:158769920
|
G | T | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+601G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769920 | ||||||
| chr4:158769921
|
A | T | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+602A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769921 | ||||||
| chr4:158769960
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107+641G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158769960 | ||||||
| chr4:158770181
|
A | AC | 130 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(127): Show | 130 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.107+864dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158770181 | |||||
| chr4:158770261
|
ATATTGCC others(15): Show |
A | 1 | a0002c0002t0003g0166 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.107+943_107+964del others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770261 | ||||||
| chr4:158770304
|
A | G | 4 | a0001c0001t0003g0036a0001c0014t0020g0035a0002c0002t0004g0037others(1): Show | 4 | HG02280.hp2 HG03225.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+985A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770304 | ||||||
| chr4:158770435
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+1116A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770435 | ||||||
| chr4:158770443
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+1124A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770443 | ||||||
| chr4:158770502
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+1183G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770502 | ||||||
| chr4:158770851
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.107+1532C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770851 | ||||||
| chr4:158770986
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.107+1667A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770986 | ||||||
| chr4:158770991
|
A | G | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+1672A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158770991 | ||||||
| chr4:158771212
|
G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+1893G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771212 | ||||||
| chr4:158771360
|
C | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+2041C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771360 | ||||||
| chr4:158771400
|
C | T | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+2081C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771400 | ||||||
| chr4:158771433
|
A | G | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+2114A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771433 | ||||||
| chr4:158771558
|
A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+2239A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158771558 | ||||||
| chr4:158772144
|
C | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(126): Show | 129 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.107+2825C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772144 | ||||||
| chr4:158772265
|
C | G | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+2946C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772265 | ||||||
| chr4:158772425
|
A | G | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+3106A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772425 | ||||||
| chr4:158772824
|
A | G | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+3505A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772824 | ||||||
| chr4:158772879
|
A | G | 6 | a0001c0001t0007g0031a0001c0001t0007g0032a0001c0007t0006g0163others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+3560A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158772879 | ||||||
| chr4:158773029
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+3710C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773029 | ||||||
| chr4:158773460
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.107+4141T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773460 | ||||||
| chr4:158773464
|
C | T | 3 | a0004c0006t0002g0246a0004c0006t0002g0247a0004c0006t0002g0248 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107+4145C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773464 | ||||||
| chr4:158773640
|
C | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+4321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773640 | ||||||
| chr4:158773717
|
C | T | 14 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+4398C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773717 | ||||||
| chr4:158773724
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.107+4405A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773724 | ||||||
| chr4:158773833
|
C | T | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+4514C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773833 | ||||||
| chr4:158773872
|
T | A | 14 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+4553T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158773872 | ||||||
| chr4:158774055
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.107+4736G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774055 | ||||||
| chr4:158774541
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.107+5222C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774541 | ||||||
| chr4:158774700
|
G | C | 1 | a0002c0002t0003g0168 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.107+5381G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774700 | ||||||
| chr4:158774952
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.107+5633C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774952 | ||||||
| chr4:158774972
|
A | T | 38 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+5653A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158774972 | ||||||
| chr4:158775265
|
C | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG00597.hp1 NA18957.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.107+5946C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775265 | ||||||
| chr4:158775799
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+6480A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775799 | ||||||
| chr4:158775822
|
T | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+6503T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158775822 | ||||||
| chr4:158776122
|
A | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(122): Show | 125 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.107+6803A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776122 | ||||||
| chr4:158776184
|
A | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+6865A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776184 | ||||||
| chr4:158776270
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107+6951A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776270 | ||||||
| chr4:158776320
|
A | G | 1 | a0011c0013t0008g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107+7001A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776320 | ||||||
| chr4:158776332
|
C | G | 4 | a0003c0004t0001g0147a0003c0004t0001g0148a0003c0004t0001g0149others(1): Show | 4 | HG02922.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+7013C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776332 | ||||||
| chr4:158776407
|
G | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7088G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776407 | ||||||
| chr4:158776427
|
A | C | 8 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0239others(5): Show | 8 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+7108A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776427 | ||||||
| chr4:158776457
|
G | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0154others(4): Show | 7 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+7138G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776457 | ||||||
| chr4:158776458
|
C | T | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0154others(4): Show | 7 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+7139C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776458 | ||||||
| chr4:158776547
|
A | G | 38 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+7228A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776547 | ||||||
| chr4:158776594
|
T | A | 77 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(74): Show | 78 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.107+7275T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776594 | ||||||
| chr4:158776662
|
GA | G | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0009t0002g0234others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+7346delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158776662 | |||||
| chr4:158776751
|
G | T | 29 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(26): Show | 29 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.107+7432G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776751 | ||||||
| chr4:158776796
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(69): Show | 73 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.107+7477G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776796 | ||||||
| chr4:158776810
|
A | C | 38 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+7491A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776810 | ||||||
| chr4:158776874
|
T | C | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7555T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776874 | ||||||
| chr4:158776934
|
A | G | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+7615A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158776934 | ||||||
| chr4:158777117
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.107+7798A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777117 | ||||||
| chr4:158777131
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+7812G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777131 | ||||||
| chr4:158777455
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107+8136A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777455 | ||||||
| chr4:158777560
|
C | T | 38 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.107+8241C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777560 | ||||||
| chr4:158777633
|
C | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+8314C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777633 | ||||||
| chr4:158777732
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+8413C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158777732 | ||||||
| chr4:158778123
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+8804C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778123 | ||||||
| chr4:158778368
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+9049C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778368 | ||||||
| chr4:158778524
|
G | A | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+9205G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778524 | ||||||
| chr4:158778534
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.107+9215G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778534 | ||||||
| chr4:158778576
|
C | T | 1 | a0001c0001t0009g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.107+9257C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778576 | ||||||
| chr4:158778598
|
GTATAT | G | 11 | a0001c0001t0001g0058a0001c0001t0001g0152a0003c0004t0001g0053others(8): Show | 11 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+9284_107+9288d others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158778598 | |||||
| chr4:158778654
|
G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+9335G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778654 | ||||||
| chr4:158778819
|
A | G | 34 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.107+9500A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778819 | ||||||
| chr4:158778908
|
G | A | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+9589G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158778908 | ||||||
| chr4:158779059
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.107+9740G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779059 | ||||||
| chr4:158779325
|
T | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG02523.hp1 NA18956.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+10006T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779325 | ||||||
| chr4:158779343
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0014g0142 | 2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107+10024C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779343 | ||||||
| chr4:158779565
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+10246G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779565 | ||||||
| chr4:158779571
|
G | GT | 6 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+10269dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779571 | |||||
| chr4:158779571
|
GT | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(228): Show | 232 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.107+10269delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779571 | |||||
| chr4:158779681
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+10362C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779681 | ||||||
| chr4:158779737
|
C | CT | 69 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0063others(66): Show | 70 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.107+10434dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779737 | |||||
| chr4:158779737
|
C | CTT | 5 | a0001c0001t0002g0227a0001c0001t0002g0230a0001c0001t0009g0231others(2): Show | 5 | HG00597.hp2 HG03669.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+10433_107+1043 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158779737 | |||||
| chr4:158779767
|
C | T | 1 | a0007c0011t0005g0004 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107+10448C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779767 | ||||||
| chr4:158779778
|
T | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+10459T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779778 | ||||||
| chr4:158779795
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG00423.hp1 HG00609.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+10476G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779795 | ||||||
| chr4:158779808
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0005g0159 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.107+10489C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158779808 | ||||||
| chr4:158780043
|
A | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107+10724A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780043 | ||||||
| chr4:158780227
|
C | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(241): Show | 245 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.107+10908C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780227 | ||||||
| chr4:158780326
|
A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+11007A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780326 | ||||||
| chr4:158780543
|
A | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+11224A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158780543 | ||||||
| chr4:158781034
|
C | CA | 13 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.107+11731dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | |||||
| chr4:158781034
|
CA | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0058others(98): Show | 101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.107+11731delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | |||||
| chr4:158781034
|
CAA | C | 73 | a0001c0001t0001g0135a0001c0001t0002g0001a0001c0001t0002g0202others(70): Show | 74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+11730_107+1173 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781034 | |||||
| chr4:158781035
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+11716A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781035 | ||||||
| chr4:158781136
|
T | C | 1 | a0001c0001t0011g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107+11817T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781136 | ||||||
| chr4:158781154
|
A | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(70): Show | 74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+11835A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781154 | ||||||
| chr4:158781213
|
C | T | 1 | a0001c0003t0004g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107+11894C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781213 | ||||||
| chr4:158781323
|
G | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+12004G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781323 | ||||||
| chr4:158781380
|
G | A | 35 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.107+12061G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781380 | ||||||
| chr4:158781553
|
C | T | 39 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(36): Show | 39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.107+12234C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781553 | ||||||
| chr4:158781758
|
C | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12439C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781758 | ||||||
| chr4:158781759
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+12440C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781759 | ||||||
| chr4:158781776
|
G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+12457G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781776 | ||||||
| chr4:158781890
|
G | GT | 12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(9): Show | 12 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+12580dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158781890 | |||||
| chr4:158781909
|
A | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12590A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781909 | ||||||
| chr4:158781922
|
G | A | 1 | a0001c0001t0008g0092 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.107+12603G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781922 | ||||||
| chr4:158781968
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.107+12649A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781968 | ||||||
| chr4:158781993
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+12674G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158781993 | ||||||
| chr4:158782073
|
T | A | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(70): Show | 74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+12754T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782073 | ||||||
| chr4:158782376
|
A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+13057A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782376 | ||||||
| chr4:158782521
|
TTG | T | 10 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0237others(7): Show | 10 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+13204_107+1320 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158782521 | |||||
| chr4:158782522
|
TG | T | 39 | a0001c0001t0002g0001a0001c0001t0002g0204a0001c0001t0002g0205others(36): Show | 40 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.107+13204delG | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782522 | ||||||
| chr4:158782535
|
T | TCCTCAAA others(306): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+13233_107+1323 others(317): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158782535 | |||||
| chr4:158782752
|
C | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+13433C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158782752 | ||||||
| chr4:158783175
|
A | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+13856A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783175 | ||||||
| chr4:158783506
|
G | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(46): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.107+14187G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783506 | ||||||
| chr4:158783720
|
G | T | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.107+14401G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783720 | ||||||
| chr4:158783751
|
A | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+14432A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783751 | ||||||
| chr4:158783904
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(111): Show | 114 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.107+14585G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158783904 | ||||||
| chr4:158784076
|
A | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+14757A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784076 | ||||||
| chr4:158784092
|
T | C | 1 | a0003c0004t0001g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.107+14773T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784092 | ||||||
| chr4:158784302
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.107+14983G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784302 | ||||||
| chr4:158784337
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+15018G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784337 | ||||||
| chr4:158784352
|
T | C | 1 | a0001c0001t0009g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+15033T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784352 | ||||||
| chr4:158784662
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.107+15343C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784662 | ||||||
| chr4:158784665
|
G | A | 6 | a0001c0001t0001g0176a0002c0002t0003g0173a0002c0002t0003g0174others(3): Show | 6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+15346G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784665 | ||||||
| chr4:158784688
|
G | A | 70 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(67): Show | 71 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.107+15369G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784688 | ||||||
| chr4:158784707
|
A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.107+15388A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784707 | ||||||
| chr4:158784714
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0005g0159 | 3 | HG02258.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+15395C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784714 | ||||||
| chr4:158784715
|
A | G | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+15396A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784715 | ||||||
| chr4:158784762
|
C | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+15443C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784762 | ||||||
| chr4:158784794
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.107+15475A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784794 | ||||||
| chr4:158784821
|
G | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | NA18955.hp2 NA18963.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.107+15502G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784821 | ||||||
| chr4:158784834
|
G | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(70): Show | 74 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.107+15515G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784834 | ||||||
| chr4:158784904
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.107+15585T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784904 | ||||||
| chr4:158784958
|
A | C | 1 | a0002c0002t0003g0197 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.107+15639A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784958 | ||||||
| chr4:158784969
|
C | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(46): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.107+15650C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158784969 | ||||||
| chr4:158785087
|
C | CT | 18 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0051others(15): Show | 18 | HG01978.hp1 HG02109.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.107+15785dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTT | 59 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(56): Show | 60 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.107+15781_107+1578 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTTT | 9 | a0001c0001t0002g0226a0001c0001t0002g0243a0001c0003t0004g0026others(6): Show | 9 | HG02145.hp2 HG02486.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+15780_107+1578 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTTTT others(3): Show |
1 | a0001c0008t0010g0034 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.107+15776_107+1578 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0003g0036a0002c0002t0003g0180a0002c0002t0003g0181others(1): Show | 4 | HG02129.hp2 HG03225.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+15775_107+1578 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTTTT others(5): Show |
29 | a0001c0001t0001g0176a0001c0001t0003g0184a0001c0014t0020g0035others(26): Show | 29 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.107+15774_107+1578 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785087
|
C | CTTTTTTT others(6): Show |
5 | a0002c0002t0003g0178a0002c0002t0003g0196a0002c0002t0004g0037others(2): Show | 5 | HG02080.hp2 HG02280.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+15773_107+1578 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785087 | |||||
| chr4:158785155
|
A | G | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+15836A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785155 | ||||||
| chr4:158785303
|
C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+15984C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785303 | ||||||
| chr4:158785374
|
G | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0058others(67): Show | 70 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.107+16055G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785374 | ||||||
| chr4:158785382
|
C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+16063C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785382 | ||||||
| chr4:158785479
|
T | C | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+16160T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785479 | ||||||
| chr4:158785516
|
A | G | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.107+16197A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785516 | ||||||
| chr4:158785621
|
G | A | 1 | a0007c0011t0005g0004 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107+16302G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785621 | ||||||
| chr4:158785710
|
C | CT | 68 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(65): Show | 69 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.107+16403dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785710 | |||||
| chr4:158785710
|
C | CTT | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0009t0002g0234others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+16402_107+1640 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158785710 | |||||
| chr4:158785714
|
T | C | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+16395T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785714 | ||||||
| chr4:158785843
|
A | G | 1 | a0006c0010t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.107+16524A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158785843 | ||||||
| chr4:158786006
|
C | T | 3 | a0001c0014t0020g0035a0002c0002t0004g0037a0002c0002t0004g0038 | 3 | HG02280.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.107+16687C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786006 | ||||||
| chr4:158786450
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+17131T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786450 | ||||||
| chr4:158786542
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.107+17223G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786542 | ||||||
| chr4:158786545
|
T | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00621.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.107+17226T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786545 | ||||||
| chr4:158786668
|
T | A | 1 | a0001c0001t0011g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+17349T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786668 | ||||||
| chr4:158786669
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107+17350A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786669 | ||||||
| chr4:158786688
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(125): Show | 128 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.107+17369G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786688 | ||||||
| chr4:158786823
|
C | T | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+17504C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786823 | ||||||
| chr4:158786886
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.107+17567C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158786886 | ||||||
| chr4:158787008
|
C | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0083others(72): Show | 76 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.107+17689C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787008 | ||||||
| chr4:158787024
|
G | C | 76 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(73): Show | 77 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.107+17705G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787024 | ||||||
| chr4:158787081
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+17762G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787081 | ||||||
| chr4:158787132
|
C | A | 15 | a0001c0001t0001g0083a0001c0003t0004g0016a0001c0003t0004g0018others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+17813C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787132 | ||||||
| chr4:158787226
|
G | A | 14 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.107+17907G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787226 | ||||||
| chr4:158787379
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+18060G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787379 | ||||||
| chr4:158787539
|
C | T | 4 | a0001c0001t0001g0127a0001c0003t0004g0125a0001c0003t0004g0126others(1): Show | 4 | HG00609.hp2 HG02135.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+18220C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787539 | ||||||
| chr4:158787826
|
C | T | 1 | a0001c0001t0018g0124 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.107+18507C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787826 | ||||||
| chr4:158787849
|
C | G | 2 | a0001c0001t0011g0068a0001c0001t0011g0070 | 2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.107+18530C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787849 | ||||||
| chr4:158787852
|
A | G | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+18533A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158787852 | ||||||
| chr4:158788348
|
A | G | 6 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+19029A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788348 | ||||||
| chr4:158788383
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 199 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.107+19064T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788383 | ||||||
| chr4:158788517
|
T | C | 1 | a0001c0003t0004g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.107+19198T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788517 | ||||||
| chr4:158788779
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+19460C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788779 | ||||||
| chr4:158788881
|
C | T | 3 | a0001c0009t0002g0234a0001c0009t0002g0235a0009c0016t0002g0236 | 3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107+19562C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788881 | ||||||
| chr4:158788938
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0014g0142 | 2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107+19619A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158788938 | ||||||
| chr4:158789019
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(196): Show | 200 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.107+19700C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789019 | ||||||
| chr4:158789092
|
G | T | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+19773G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789092 | ||||||
| chr4:158789180
|
G | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 199 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.107+19861G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789180 | ||||||
| chr4:158789239
|
C | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+19920C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789239 | ||||||
| chr4:158789315
|
GTGTGTA | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(63): Show | 67 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.107+20002_107+2000 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789315 | |||||
| chr4:158789321
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(127): Show | 130 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.107+20002A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789321 | ||||||
| chr4:158789325
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 185 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.107+20006G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789325 | ||||||
| chr4:158789325
|
G | GTA | 11 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0119others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.107+20007_107+2000 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789325 | |||||
| chr4:158789644
|
C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+20325C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789644 | ||||||
| chr4:158789677
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.107+20358C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789677 | ||||||
| chr4:158789739
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+20420C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158789739 | ||||||
| chr4:158789826
|
G | GCCTATTA others(3): Show |
198 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 199 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.107+20510_107+2051 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158789826 | |||||
| chr4:158790057
|
A | G | 3 | a0002c0002t0003g0193a0002c0002t0003g0194a0002c0002t0003g0195 | 3 | NA18951.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.107+20738A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790057 | ||||||
| chr4:158790242
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+20923C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790242 | ||||||
| chr4:158790294
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.107+20975G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790294 | ||||||
| chr4:158790738
|
C | A | 36 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+21419C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790738 | ||||||
| chr4:158790789
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.107+21470G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158790789 | ||||||
| chr4:158791072
|
G | A | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107+21753G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791072 | ||||||
| chr4:158791118
|
GA | G | 44 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(41): Show | 45 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.107+21800delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791118 | ||||||
| chr4:158791266
|
CT | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.107+21976delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTT | C | 9 | a0001c0001t0001g0130a0001c0001t0001g0152a0001c0001t0001g0154others(6): Show | 9 | HG01192.hp2 HG01255.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+21975_107+2197 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTTT | C | 36 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0176others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+21974_107+2197 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTTTTTTT others(6): Show |
C | 12 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0020others(9): Show | 12 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+21964_107+2197 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0003t0004g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.107+21963_107+2197 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+21961_107+2197 others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791266
|
CTTTTTTT others(11): Show |
C | 54 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(51): Show | 55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.107+21959_107+2197 others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791266 | |||||
| chr4:158791282
|
TTTTTTTT others(7): Show |
T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107+21969_107+2198 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791282 | |||||
| chr4:158791283
|
TTTTTTTT others(6): Show |
T | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+21970_107+2198 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158791283 | |||||
| chr4:158791340
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+22021A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791340 | ||||||
| chr4:158791441
|
G | C | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107+22122G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791441 | ||||||
| chr4:158791573
|
C | T | 1 | a0001c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.107+22254C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791573 | ||||||
| chr4:158791888
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.107+22569G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791888 | ||||||
| chr4:158791905
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+22586C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791905 | ||||||
| chr4:158791933
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.107+22614G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158791933 | ||||||
| chr4:158792053
|
G | A | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+22734G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792053 | ||||||
| chr4:158792122
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107+22803C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792122 | ||||||
| chr4:158792203
|
A | G | 1 | a0004c0006t0002g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.107+22884A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792203 | ||||||
| chr4:158792216
|
C | T | 2 | a0002c0002t0003g0181a0002c0002t0003g0182 | 2 | HG02129.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.107+22897C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792216 | ||||||
| chr4:158792288
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.107+22969C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792288 | ||||||
| chr4:158792359
|
A | C | 4 | a0001c0001t0001g0152a0003c0004t0001g0054a0003c0004t0001g0055others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+23040A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792359 | ||||||
| chr4:158792372
|
C | CT | 6 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0002g0226others(3): Show | 6 | HG00735.hp2 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+23069dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158792372 | |||||
| chr4:158792482
|
A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.107+23163A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792482 | ||||||
| chr4:158792496
|
T | C | 1 | a0003c0004t0001g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107+23177T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158792496 | ||||||
| chr4:158793272
|
G | A | 7 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+23953G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158793272 | ||||||
| chr4:158794328
|
A | AT | 67 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0058others(64): Show | 67 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.107+25017dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158794328 | |||||
| chr4:158794329
|
T | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+25010T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794329 | ||||||
| chr4:158794414
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.107+25095G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794414 | ||||||
| chr4:158794428
|
C | T | 1 | a0001c0001t0011g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.107+25109C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794428 | ||||||
| chr4:158794457
|
C | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107+25138C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794457 | ||||||
| chr4:158794505
|
A | G | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.107+25186A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794505 | ||||||
| chr4:158794526
|
G | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.107+25207G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158794526 | ||||||
| chr4:158795011
|
A | G | 1 | a0001c0001t0011g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.107+25692A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795011 | ||||||
| chr4:158795189
|
C | T | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+25870C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795189 | ||||||
| chr4:158795349
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.107+26030G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158795349 | ||||||
| chr4:158796253
|
G | A | 1 | a0001c0001t0009g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+26934G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158796253 | ||||||
| chr4:158796406
|
CTTA | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+27090_107+2709 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158796406 | |||||
| chr4:158796460
|
T | G | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(3): Show | 6 | HG00621.hp2 NA18951.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+27141T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158796460 | ||||||
| chr4:158797007
|
T | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01167.hp1 HG01169.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.107+27688T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797007 | ||||||
| chr4:158797303
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107+27984C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797303 | ||||||
| chr4:158797362
|
T | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.107+28043T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797362 | ||||||
| chr4:158797499
|
A | C | 3 | a0001c0008t0010g0033a0001c0008t0010g0034a0001c0014t0020g0035 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107+28180A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797499 | ||||||
| chr4:158797527
|
C | T | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107+28208C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158797527 | ||||||
| chr4:158798010
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108-27906T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798010 | ||||||
| chr4:158798140
|
C | G | 37 | a0001c0001t0001g0176a0001c0001t0003g0036a0001c0001t0003g0184others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.108-27776C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798140 | ||||||
| chr4:158798165
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.108-27751A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798165 | ||||||
| chr4:158798387
|
A | C | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.108-27529A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798387 | ||||||
| chr4:158798792
|
T | TAACACA | 6 | a0001c0001t0001g0176a0002c0002t0003g0173a0002c0002t0003g0174others(3): Show | 6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-27123_108-2711 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158798792 | |||||
| chr4:158798803
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0006c0010t0001g0128 | 3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.108-27113A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158798803 | ||||||
| chr4:158799745
|
CT | C | 6 | a0001c0003t0004g0016a0001c0003t0004g0026a0001c0003t0013g0027others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-26169delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158799745 | |||||
| chr4:158799976
|
C | T | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-25940C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158799976 | ||||||
| chr4:158800141
|
T | G | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-25775T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800141 | ||||||
| chr4:158800192
|
C | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-25724C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800192 | ||||||
| chr4:158800302
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-25614A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800302 | ||||||
| chr4:158800364
|
T | C | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.108-25552T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800364 | ||||||
| chr4:158800615
|
T | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(46): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.108-25301T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800615 | ||||||
| chr4:158800723
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-25193T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800723 | ||||||
| chr4:158800733
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.108-25183T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800733 | ||||||
| chr4:158800824
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.108-25092A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800824 | ||||||
| chr4:158800996
|
A | G | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-24920A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158800996 | ||||||
| chr4:158801425
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.108-24491A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158801425 | ||||||
| chr4:158801565
|
C | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-24351C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158801565 | ||||||
| chr4:158802000
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-23916C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802000 | ||||||
| chr4:158802009
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.108-23907A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802009 | ||||||
| chr4:158802094
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108-23822G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802094 | ||||||
| chr4:158802417
|
G | A | 1 | a0001c0001t0005g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.108-23499G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802417 | ||||||
| chr4:158802516
|
G | A | 3 | a0003c0004t0001g0147a0003c0004t0001g0148a0003c0004t0001g0149 | 3 | HG03453.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.108-23400G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802516 | ||||||
| chr4:158802591
|
G | T | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.108-23325G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802591 | ||||||
| chr4:158802905
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.108-23011G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158802905 | ||||||
| chr4:158803032
|
G | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-22884G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803032 | ||||||
| chr4:158803063
|
C | T | 3 | a0001c0001t0007g0031a0001c0001t0007g0032a0010c0015t0004g0013 | 3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-22853C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803063 | ||||||
| chr4:158803140
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0116 | 2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.108-22776T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803140 | ||||||
| chr4:158803204
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-22712A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803204 | ||||||
| chr4:158803594
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.108-22322T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803594 | ||||||
| chr4:158803597
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.108-22319C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803597 | ||||||
| chr4:158803629
|
A | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(241): Show | 245 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.108-22287A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803629 | ||||||
| chr4:158803782
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108-22134A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803782 | ||||||
| chr4:158803817
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.108-22099A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158803817 | ||||||
| chr4:158804153
|
G | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-21763G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804153 | ||||||
| chr4:158804413
|
C | CT | 221 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(218): Show | 222 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.108-21486dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158804413 | |||||
| chr4:158804413
|
C | CTT | 15 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0060others(12): Show | 15 | HG00597.hp2 HG00735.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-21487_108-2148 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158804413 | |||||
| chr4:158804432
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.108-21484G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804432 | ||||||
| chr4:158804613
|
A | T | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-21303A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804613 | ||||||
| chr4:158804667
|
C | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-21249C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804667 | ||||||
| chr4:158804897
|
A | T | 1 | a0001c0001t0019g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.108-21019A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158804897 | ||||||
| chr4:158805051
|
C | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-20865C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805051 | ||||||
| chr4:158805123
|
A | G | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-20793A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805123 | ||||||
| chr4:158805132
|
G | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-20784G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805132 | ||||||
| chr4:158805147
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0008g0092 | 2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.108-20769A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805147 | ||||||
| chr4:158805193
|
T | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(123): Show | 126 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.108-20723T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805193 | ||||||
| chr4:158805390
|
T | C | 1 | a0001c0003t0004g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.108-20526T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805390 | ||||||
| chr4:158805411
|
A | G | 1 | a0007c0011t0005g0004 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.108-20505A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805411 | ||||||
| chr4:158805446
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-20470G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805446 | ||||||
| chr4:158805800
|
C | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-20116C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805800 | ||||||
| chr4:158805898
|
T | G | 3 | a0001c0009t0002g0234a0001c0009t0002g0235a0009c0016t0002g0236 | 3 | HG01884.hp2 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.108-20018T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805898 | ||||||
| chr4:158805913
|
A | G | 57 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(54): Show | 58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.108-20003A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158805913 | ||||||
| chr4:158806040
|
C | CT | 79 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(76): Show | 79 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.108-19863dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158806040 | |||||
| chr4:158806292
|
G | A | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.108-19624G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806292 | ||||||
| chr4:158806292
|
G | T | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-19624G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806292 | ||||||
| chr4:158806525
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.108-19391A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806525 | ||||||
| chr4:158806944
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.108-18972A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158806944 | ||||||
| chr4:158807147
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.108-18769C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807147 | ||||||
| chr4:158807486
|
G | A | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.108-18430G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807486 | ||||||
| chr4:158807558
|
A | G | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108-18358A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807558 | ||||||
| chr4:158807994
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-17922C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158807994 | ||||||
| chr4:158808104
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-17812A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808104 | ||||||
| chr4:158808359
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0019g0111 | 2 | HG01934.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.108-17557A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808359 | ||||||
| chr4:158808544
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.108-17372G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808544 | ||||||
| chr4:158808642
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0043others(63): Show | 66 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.108-17274C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808642 | ||||||
| chr4:158808761
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.108-17155C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808761 | ||||||
| chr4:158808801
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.108-17115G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808801 | ||||||
| chr4:158808831
|
T | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-17085T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808831 | ||||||
| chr4:158808858
|
A | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-17058A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158808858 | ||||||
| chr4:158809191
|
G | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-16725G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809191 | ||||||
| chr4:158809310
|
T | G | 2 | a0002c0002t0007g0169a0002c0002t0007g0170 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.108-16606T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809310 | ||||||
| chr4:158809328
|
A | G | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-16588A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809328 | ||||||
| chr4:158809385
|
G | C | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-16531G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809385 | ||||||
| chr4:158809630
|
T | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0073others(5): Show | 8 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-16286T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809630 | ||||||
| chr4:158809656
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0014g0142 | 2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.108-16260C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158809656 | ||||||
| chr4:158810151
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.108-15765C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810151 | ||||||
| chr4:158810667
|
C | T | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.108-15249C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810667 | ||||||
| chr4:158810885
|
G | A | 5 | a0001c0001t0002g0237a0001c0007t0006g0012a0001c0007t0006g0163others(2): Show | 5 | HG01934.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-15031G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158810885 | ||||||
| chr4:158811519
|
T | C | 117 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0176others(114): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.108-14397T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811519 | ||||||
| chr4:158811541
|
T | C | 97 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0176others(94): Show | 98 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.108-14375T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811541 | ||||||
| chr4:158811551
|
T | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.108-14365T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811551 | ||||||
| chr4:158811555
|
T | TTAATAA | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-14353_108-1434 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158811555 | |||||
| chr4:158811622
|
G | A | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-14294G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811622 | ||||||
| chr4:158811659
|
T | TAC | 54 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(51): Show | 55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.108-14243_108-1424 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158811659 | |||||
| chr4:158811696
|
G | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-14220G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811696 | ||||||
| chr4:158811736
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0008g0047 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.108-14180C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811736 | ||||||
| chr4:158811882
|
C | T | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108-14034C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158811882 | ||||||
| chr4:158812064
|
A | G | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.108-13852A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812064 | ||||||
| chr4:158812089
|
C | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.108-13827C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812089 | ||||||
| chr4:158812346
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0002g0226 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.108-13570C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812346 | ||||||
| chr4:158812347
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-13569G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812347 | ||||||
| chr4:158812495
|
A | G | 2 | a0001c0001t0012g0088a0001c0001t0012g0089 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.108-13421A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812495 | ||||||
| chr4:158812555
|
T | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-13361T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812555 | ||||||
| chr4:158812589
|
T | G | 3 | a0001c0001t0002g0204a0001c0001t0002g0209a0001c0001t0002g0249 | 3 | HG00280.hp2 HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.108-13327T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812589 | ||||||
| chr4:158812898
|
C | T | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-13018C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812898 | ||||||
| chr4:158812944
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.108-12972T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158812944 | ||||||
| chr4:158813222
|
C | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.108-12694C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813222 | ||||||
| chr4:158813534
|
A | G | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-12382A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813534 | ||||||
| chr4:158813840
|
G | C | 1 | a0001c0003t0004g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-12076G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158813840 | ||||||
| chr4:158814346
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.108-11570G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814346 | ||||||
| chr4:158814348
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.108-11568G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814348 | ||||||
| chr4:158814429
|
C | G | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-11487C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814429 | ||||||
| chr4:158814891
|
A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-11025A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158814891 | ||||||
| chr4:158815250
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-10666G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815250 | ||||||
| chr4:158815384
|
C | CT | 60 | a0001c0001t0001g0095a0001c0001t0002g0001a0001c0001t0002g0202others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.108-10516dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158815384 | |||||
| chr4:158815524
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-10392A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815524 | ||||||
| chr4:158815655
|
C | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.108-10261C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815655 | ||||||
| chr4:158815960
|
A | G | 54 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(51): Show | 55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.108-9956A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158815960 | ||||||
| chr4:158816071
|
G | GTA | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-9831_108-9830d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158816071 | |||||
| chr4:158816075
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108-9841A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816075 | ||||||
| chr4:158816145
|
G | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-9771G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816145 | ||||||
| chr4:158816585
|
C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-9331C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816585 | ||||||
| chr4:158816634
|
A | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0072others(4): Show | 7 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-9282A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816634 | ||||||
| chr4:158816756
|
G | C | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.108-9160G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816756 | ||||||
| chr4:158816784
|
CA | C | 100 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0119others(97): Show | 101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.108-9115delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158816784 | |||||
| chr4:158816809
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-9107A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816809 | ||||||
| chr4:158816959
|
T | G | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-8957T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816959 | ||||||
| chr4:158816969
|
T | G | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-8947T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158816969 | ||||||
| chr4:158817057
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-8859A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817057 | ||||||
| chr4:158817586
|
G | A | 1 | a0001c0003t0004g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.108-8330G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817586 | ||||||
| chr4:158817662
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.108-8254T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817662 | ||||||
| chr4:158817793
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108-8123C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817793 | ||||||
| chr4:158817797
|
G | A | 1 | a0003c0004t0001g0150 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-8119G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158817797 | ||||||
| chr4:158818048
|
T | C | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.108-7868T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818048 | ||||||
| chr4:158818542
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-7374A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818542 | ||||||
| chr4:158818731
|
T | A | 1 | a0008c0012t0002g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108-7185T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818731 | ||||||
| chr4:158818937
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.108-6979G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158818937 | ||||||
| chr4:158819112
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.108-6804G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819112 | ||||||
| chr4:158819142
|
C | T | 1 | a0002c0002t0007g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.108-6774C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819142 | ||||||
| chr4:158819287
|
G | C | 3 | a0001c0001t0001g0152a0003c0004t0001g0054a0003c0004t0001g0055 | 3 | HG02622.hp1 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.108-6629G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819287 | ||||||
| chr4:158819295
|
A | G | 10 | a0001c0001t0001g0152a0003c0004t0001g0053a0003c0004t0001g0054others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.108-6621A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819295 | ||||||
| chr4:158819398
|
AATTAAT | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.108-6509_108-6504d others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158819398 | |||||
| chr4:158819455
|
T | A | 1 | a0008c0012t0002g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108-6461T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819455 | ||||||
| chr4:158819891
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.108-6025A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158819891 | ||||||
| chr4:158820253
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.108-5663C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820253 | ||||||
| chr4:158820280
|
T | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.108-5636T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820280 | ||||||
| chr4:158820292
|
G | A | 6 | a0002c0002t0003g0168a0002c0002t0003g0187a0002c0002t0003g0188others(3): Show | 6 | NA18951.hp2 NA19004.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-5624G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820292 | ||||||
| chr4:158820391
|
G | A | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-5525G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820391 | ||||||
| chr4:158820648
|
C | T | 35 | a0001c0001t0001g0176a0001c0001t0003g0184a0002c0002t0003g0166others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.108-5268C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158820648 | ||||||
| chr4:158820710
|
TA | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.108-5204delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158820710 | |||||
| chr4:158821121
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108-4795A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821121 | ||||||
| chr4:158821256
|
G | T | 1 | a0001c0001t0014g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.108-4660G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821256 | ||||||
| chr4:158821274
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.108-4642A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821274 | ||||||
| chr4:158821994
|
A | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0087 | 2 | HG02257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.108-3922A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158821994 | ||||||
| chr4:158822034
|
A | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.108-3882A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822034 | ||||||
| chr4:158822044
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-3872C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822044 | ||||||
| chr4:158822174
|
C | CT | 59 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0052others(56): Show | 60 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.108-3721dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158822174 | |||||
| chr4:158822174
|
CT | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0093a0001c0007t0006g0012others(7): Show | 10 | HG01943.hp2 HG02055.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-3721delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158822174 | |||||
| chr4:158822273
|
G | A | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-3643G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822273 | ||||||
| chr4:158822427
|
G | A | 2 | a0003c0004t0001g0053a0003c0004t0001g0056 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.108-3489G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822427 | ||||||
| chr4:158822474
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.108-3442C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822474 | ||||||
| chr4:158822475
|
G | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-3441G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822475 | ||||||
| chr4:158822481
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-3435T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158822481 | ||||||
| chr4:158823316
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2600A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823316 | ||||||
| chr4:158823341
|
C | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108-2575C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823341 | ||||||
| chr4:158823486
|
G | C | 1 | a0002c0002t0004g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108-2430G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823486 | ||||||
| chr4:158823612
|
G | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2304G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158823612 | ||||||
| chr4:158824017
|
C | T | 57 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(54): Show | 58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.108-1899C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824017 | ||||||
| chr4:158824724
|
G | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.108-1192G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824724 | ||||||
| chr4:158824756
|
CT | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-1157delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 158824756 | |||||
| chr4:158824764
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-1152C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158824764 | ||||||
| chr4:158825480
|
G | C | 1 | a0001c0001t0002g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.108-436G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158825480 | ||||||
| chr4:158825585
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108-331T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 1/16 | chr4 | 158825585 | ||||||
| chr4:158826101
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.234+59C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826101 | ||||||
| chr4:158826197
|
C | G | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234+155C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826197 | ||||||
| chr4:158826301
|
C | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+259C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826301 | ||||||
| chr4:158826462
|
C | T | 1 | a0002c0002t0003g0195 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.234+420C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826462 | ||||||
| chr4:158826616
|
AGTG | A | 8 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0239others(5): Show | 8 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+593_234+595del others(3): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr4 | 158826616 | |||||
| chr4:158826834
|
C | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.234+792C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826834 | ||||||
| chr4:158826880
|
A | G | 1 | a0002c0002t0003g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.234+838A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158826880 | ||||||
| chr4:158827001
|
A | G | 6 | a0002c0002t0003g0168a0002c0002t0003g0187a0002c0002t0003g0188others(3): Show | 6 | NA18951.hp2 NA19004.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+959A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827001 | ||||||
| chr4:158827064
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+1022C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827064 | ||||||
| chr4:158827303
|
T | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+1261T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827303 | ||||||
| chr4:158827458
|
T | G | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+1416T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827458 | ||||||
| chr4:158827511
|
G | A | 1 | a0001c0003t0004g0125 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.234+1469G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827511 | ||||||
| chr4:158827872
|
A | G | 7 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0219others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-1207A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827872 | ||||||
| chr4:158827899
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.235-1180A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827899 | ||||||
| chr4:158827968
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-1111A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158827968 | ||||||
| chr4:158828014
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.235-1065T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828014 | ||||||
| chr4:158828344
|
C | T | 1 | a0006c0010t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.235-735C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828344 | ||||||
| chr4:158828345
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-734G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828345 | ||||||
| chr4:158828636
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.235-443A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828636 | ||||||
| chr4:158828820
|
T | C | 7 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(4): Show | 7 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-259T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828820 | ||||||
| chr4:158828878
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-201C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 2/16 | chr4 | 158828878 | ||||||
| chr4:158829392
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.381+167G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829392 | ||||||
| chr4:158829647
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+422G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829647 | ||||||
| chr4:158829711
|
G | GGT | 20 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0048others(17): Show | 20 | HG02055.hp1 HG02486.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.381+511_381+512dup others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | |||||
| chr4:158829711
|
G | GGTGT | 3 | a0001c0003t0004g0024a0001c0003t0004g0125a0001c0003t0004g0134 | 3 | HG00609.hp2 HG02683.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.381+509_381+512dup others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | |||||
| chr4:158829711
|
GGT | G | 33 | a0001c0001t0001g0161a0001c0001t0003g0036a0002c0002t0003g0166others(30): Show | 33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+511_381+512del others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158829711 | |||||
| chr4:158829713
|
T | G | 6 | a0001c0001t0001g0153a0001c0001t0005g0006a0001c0007t0006g0012others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+488T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829713 | ||||||
| chr4:158829747
|
G | A | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.381+522G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829747 | ||||||
| chr4:158829845
|
T | C | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+620T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829845 | ||||||
| chr4:158829903
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.381+678A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829903 | ||||||
| chr4:158829919
|
C | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.381+694C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158829919 | ||||||
| chr4:158830001
|
A | T | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.381+776A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830001 | ||||||
| chr4:158830082
|
T | G | 1 | a0001c0001t0018g0124 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.381+857T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830082 | ||||||
| chr4:158830116
|
G | C | 2 | a0001c0001t0002g0219a0001c0001t0002g0223 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.381+891G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830116 | ||||||
| chr4:158830123
|
G | A | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+898G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830123 | ||||||
| chr4:158830173
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.381+948A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830173 | ||||||
| chr4:158830210
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+985G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830210 | ||||||
| chr4:158830235
|
T | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+1010T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830235 | ||||||
| chr4:158830248
|
C | CT | 9 | a0001c0001t0001g0152a0003c0004t0001g0053a0003c0004t0001g0054others(6): Show | 9 | HG01981.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+1048dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | |||||
| chr4:158830248
|
CT | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(153): Show | 157 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.381+1048delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | |||||
| chr4:158830248
|
CTT | C | 58 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0079others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.381+1047_381+1048d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr4 | 158830248 | |||||
| chr4:158830278
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+1053C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830278 | ||||||
| chr4:158830299
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+1074A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830299 | ||||||
| chr4:158830316
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.381+1091G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830316 | ||||||
| chr4:158830329
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.381+1104C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830329 | ||||||
| chr4:158830388
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+1163G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830388 | ||||||
| chr4:158830424
|
G | A | 3 | a0001c0001t0007g0031a0001c0001t0007g0032a0010c0015t0004g0013 | 3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+1199G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830424 | ||||||
| chr4:158830551
|
C | T | 3 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242 | 3 | NA18963.hp2 NA18972.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.382-1310C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830551 | ||||||
| chr4:158830583
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.382-1278G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830583 | ||||||
| chr4:158830707
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-1154T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830707 | ||||||
| chr4:158830795
|
A | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01255.hp2 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-1066A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830795 | ||||||
| chr4:158830855
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-1006G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830855 | ||||||
| chr4:158830926
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.382-935C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830926 | ||||||
| chr4:158830976
|
G | C | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382-885G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158830976 | ||||||
| chr4:158831037
|
G | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382-824G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831037 | ||||||
| chr4:158831219
|
A | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(2): Show | 5 | HG03471.hp2 HG04228.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-642A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831219 | ||||||
| chr4:158831513
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.382-348A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831513 | ||||||
| chr4:158831689
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-172G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 3/16 | chr4 | 158831689 | ||||||
| chr4:158832192
|
A | G | 2 | a0001c0001t0002g0238a0001c0001t0009g0244 | 2 | HG00597.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.554+54A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832192 | ||||||
| chr4:158832254
|
T | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.554+116T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832254 | ||||||
| chr4:158832423
|
A | G | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063others(5): Show | 8 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+285A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832423 | ||||||
| chr4:158832770
|
T | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.554+632T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832770 | ||||||
| chr4:158832929
|
T | C | 2 | a0001c0001t0005g0006a0001c0001t0005g0008 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.555-599T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158832929 | ||||||
| chr4:158833197
|
G | T | 1 | a0001c0001t0002g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.555-331G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833197 | ||||||
| chr4:158833208
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0074 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.555-320T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833208 | ||||||
| chr4:158833432
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.555-96C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833432 | ||||||
| chr4:158833499
|
C | A | 1 | a0001c0001t0012g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.555-29C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 5/16 | chr4 | 158833499 | ||||||
| chr4:158833713
|
G | GT | 23 | a0001c0001t0001g0137a0001c0001t0008g0092a0001c0003t0004g0016others(20): Show | 23 | HG00609.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.655+96dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158833713 | |||||
| chr4:158833727
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.655+99G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158833727 | ||||||
| chr4:158833792
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.655+164C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158833792 | ||||||
| chr4:158834012
|
T | C | 1 | a0002c0002t0003g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.655+384T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834012 | ||||||
| chr4:158834025
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+397C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834025 | ||||||
| chr4:158834084
|
G | A | 1 | a0002c0002t0003g0166 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.655+456G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834084 | ||||||
| chr4:158834140
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.655+512G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834140 | ||||||
| chr4:158834246
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655+618C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834246 | ||||||
| chr4:158834288
|
T | TTC | 3 | a0001c0001t0001g0072a0002c0002t0003g0175a0007c0011t0005g0004 | 3 | HG01981.hp2 HG03491.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.655+701_655+702dup others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTC | 12 | a0001c0001t0001g0084a0001c0001t0001g0127a0001c0001t0002g0249others(9): Show | 12 | HG00423.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+699_655+702dup others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTC | 14 | a0001c0001t0002g0202a0001c0001t0003g0184a0002c0002t0003g0166others(11): Show | 14 | HG00280.hp1 HG00738.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+697_655+702dup others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(1): Show |
9 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0122others(6): Show | 9 | HG00735.hp1 HG00738.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+695_655+702dup others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(3): Show |
29 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0077others(26): Show | 29 | HG00609.hp1 HG00639.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.655+693_655+702dup others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(5): Show |
43 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0049others(40): Show | 44 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.655+691_655+702dup others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(7): Show |
34 | a0001c0001t0001g0039a0001c0001t0001g0071a0001c0001t0001g0076others(31): Show | 34 | HG00280.hp2 HG00642.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.655+689_655+702dup others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(9): Show |
28 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0065others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.655+687_655+702dup others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(11): Show |
14 | a0001c0001t0001g0052a0001c0001t0001g0066a0001c0001t0001g0067others(11): Show | 14 | HG01261.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+685_655+702dup others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(13): Show |
9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0058others(6): Show | 9 | HG00597.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+683_655+702dup others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(15): Show |
3 | a0001c0001t0001g0064a0003c0004t0001g0054a0003c0004t0001g0056 | 3 | HG02717.hp1 NA18906.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.655+681_655+702dup others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(17): Show |
3 | a0001c0001t0001g0043a0001c0001t0012g0088a0003c0004t0001g0057 | 3 | HG02109.hp2 HG02145.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.655+679_655+702dup others(24): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(19): Show |
2 | a0001c0001t0001g0090a0001c0001t0019g0111 | 2 | HG01934.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.655+677_655+702dup others(26): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(23): Show |
1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.655+673_655+702dup others(30): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
T | TTCTCTCT others(13): Show |
1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.655+677_655+678ins others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
TTC | T | 9 | a0001c0001t0001g0101a0001c0001t0002g0238a0001c0001t0005g0005others(6): Show | 9 | HG00558.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+701_655+702del others(2): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834288
|
TTCTCTC | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0005g0159 | 3 | HG02258.hp1 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.655+697_655+702del others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834288 | |||||
| chr4:158834313
|
TCTCTCTC others(11): Show |
T | 3 | a0001c0007t0006g0012a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02145.hp2 HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.655+692_655+709del others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834313 | |||||
| chr4:158834317
|
TCTCTCTC others(7): Show |
T | 1 | a0001c0007t0006g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655+696_655+709del others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834317 | |||||
| chr4:158834325
|
T | TCTCTCTC others(11): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834325 | |||||
| chr4:158834329
|
T | TCTCTCTC others(7): Show |
2 | a0001c0003t0004g0020a0001c0003t0004g0021 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834329 | |||||
| chr4:158834329
|
T | TCTCTCTC others(11): Show |
1 | a0003c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 158834329 | |||||
| chr4:158834330
|
C | CTCTCTCT others(2): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0138a0002c0002t0004g0037 | 3 | HG02280.hp2 HG03225.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(4): Show |
7 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0105others(4): Show | 7 | HG00642.hp2 HG01192.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+702_655+703ins others(11): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(6): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0155a0004c0006t0002g0248 | 3 | HG01258.hp1 HG01975.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(13): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(8): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0123 | 2 | HG02148.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(10): Show |
1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.655+702_655+703ins others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(12): Show |
2 | a0001c0001t0004g0136a0003c0004t0001g0149 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.655+702_655+703ins others(19): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834330
|
C | CTCTCTCT others(14): Show |
1 | a0001c0001t0001g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.655+702_655+703ins others(21): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834330 | ||||||
| chr4:158834331
|
C | T | 1 | a0002c0002t0003g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.655+703C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834331 | ||||||
| chr4:158834342
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+714A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834342 | ||||||
| chr4:158834841
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.656-564T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158834841 | ||||||
| chr4:158835018
|
C | T | 33 | a0002c0002t0003g0166a0002c0002t0003g0167a0002c0002t0003g0168others(30): Show | 33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.656-387C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835018 | ||||||
| chr4:158835393
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.656-12C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835393 | ||||||
| chr4:158835395
|
T | G | 1 | a0001c0001t0002g0230 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.656-10T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 6/16 | chr4 | 158835395 | ||||||
| chr4:158836168
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.727+692T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836168 | ||||||
| chr4:158836423
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.727+947G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836423 | ||||||
| chr4:158836644
|
CA | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.727+1182delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836644 | |||||
| chr4:158836677
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1201G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836677 | ||||||
| chr4:158836693
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727+1217A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836693 | ||||||
| chr4:158836811
|
C | CA | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0043others(16): Show | 19 | HG00597.hp1 HG01192.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.727+1362dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | |||||
| chr4:158836811
|
CA | C | 89 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(86): Show | 90 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.727+1362delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | |||||
| chr4:158836811
|
CAA | C | 51 | a0001c0001t0001g0085a0001c0001t0007g0031a0001c0001t0007g0032others(48): Show | 51 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.727+1361_727+1362d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | |||||
| chr4:158836811
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0003g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.727+1349_727+1362d others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158836811 | |||||
| chr4:158836927
|
T | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1451T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158836927 | ||||||
| chr4:158837441
|
A | G | 7 | a0002c0002t0003g0171a0002c0002t0003g0172a0002c0002t0004g0037others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1965A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837441 | ||||||
| chr4:158837764
|
G | A | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.727+2288G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837764 | ||||||
| chr4:158837928
|
G | A | 3 | a0001c0001t0007g0031a0001c0001t0007g0032a0010c0015t0004g0013 | 3 | HG02615.hp2 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.727+2452G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837928 | ||||||
| chr4:158837974
|
G | A | 36 | a0002c0002t0003g0166a0002c0002t0003g0167a0002c0002t0003g0168others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.727+2498G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158837974 | ||||||
| chr4:158838101
|
A | AATTGTGT others(14): Show |
1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+2627_727+2647d others(23): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838101 | |||||
| chr4:158838229
|
C | CT | 114 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(111): Show | 114 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.727+2772dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838229 | |||||
| chr4:158838229
|
CT | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0145others(54): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.727+2772delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158838229 | |||||
| chr4:158838339
|
G | A | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.727+2863G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838339 | ||||||
| chr4:158838391
|
T | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(1): Show | 4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+2915T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838391 | ||||||
| chr4:158838497
|
A | G | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.727+3021A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838497 | ||||||
| chr4:158838545
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.727+3069G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838545 | ||||||
| chr4:158838761
|
T | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+3285T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158838761 | ||||||
| chr4:158839124
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0008g0092 | 2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.727+3648C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839124 | ||||||
| chr4:158839200
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.727+3724C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839200 | ||||||
| chr4:158839357
|
A | ATTAT | 8 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0008t0010g0033others(5): Show | 8 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.727+3896_727+3899d others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158839357 | |||||
| chr4:158839357
|
A | ATTATTTA others(1): Show |
46 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(43): Show | 47 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.727+3892_727+3899d others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158839357 | |||||
| chr4:158839577
|
C | T | 20 | a0001c0001t0007g0031a0001c0001t0007g0032a0001c0003t0004g0016others(17): Show | 20 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.727+4101C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839577 | ||||||
| chr4:158839831
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(241): Show | 245 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.727+4355A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158839831 | ||||||
| chr4:158840132
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02523.hp1 NA18956.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.727+4656G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840132 | ||||||
| chr4:158840200
|
T | C | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.727+4724T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840200 | ||||||
| chr4:158840240
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+4764C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840240 | ||||||
| chr4:158840330
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.727+4854G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840330 | ||||||
| chr4:158840394
|
TTTG | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+4927_727+4929d others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr4 | 158840394 | |||||
| chr4:158840457
|
G | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp1 HG00609.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+4981G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840457 | ||||||
| chr4:158840541
|
G | A | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727+5065G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840541 | ||||||
| chr4:158840756
|
T | G | 1 | a0002c0002t0003g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.727+5280T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840756 | ||||||
| chr4:158840839
|
A | C | 1 | a0002c0002t0007g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.727+5363A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158840839 | ||||||
| chr4:158841208
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+5732T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841208 | ||||||
| chr4:158841280
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+5804G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841280 | ||||||
| chr4:158841478
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(1): Show | 4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+6002G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841478 | ||||||
| chr4:158841683
|
A | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.727+6207A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841683 | ||||||
| chr4:158841777
|
G | A | 1 | a0007c0011t0005g0004 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.727+6301G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841777 | ||||||
| chr4:158841957
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+6481G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841957 | ||||||
| chr4:158841978
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0002g0217 | 2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.727+6502A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158841978 | ||||||
| chr4:158842044
|
T | G | 1 | a0004c0006t0002g0247 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.727+6568T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842044 | ||||||
| chr4:158842147
|
T | C | 37 | a0001c0001t0003g0184a0002c0002t0003g0166a0002c0002t0003g0167others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.727+6671T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842147 | ||||||
| chr4:158842184
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.727+6708A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842184 | ||||||
| chr4:158842215
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0006c0010t0001g0128 | 3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.727+6739A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842215 | ||||||
| chr4:158842388
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.727+6912A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842388 | ||||||
| chr4:158842483
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+7007T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842483 | ||||||
| chr4:158842577
|
G | A | 1 | a0002c0002t0004g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.727+7101G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842577 | ||||||
| chr4:158842611
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.727+7135C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842611 | ||||||
| chr4:158842616
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.727+7140A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842616 | ||||||
| chr4:158842687
|
A | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727+7211A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158842687 | ||||||
| chr4:158843145
|
C | G | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727+7669C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158843145 | ||||||
| chr4:158843710
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-7611T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158843710 | ||||||
| chr4:158844044
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.728-7277T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844044 | ||||||
| chr4:158844132
|
G | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-7189G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844132 | ||||||
| chr4:158844209
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-7112A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844209 | ||||||
| chr4:158844285
|
A | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0073others(5): Show | 8 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.728-7036A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844285 | ||||||
| chr4:158844517
|
C | G | 1 | a0002c0002t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.728-6804C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844517 | ||||||
| chr4:158844798
|
A | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.728-6523A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158844798 | ||||||
| chr4:158845009
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.728-6312G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845009 | ||||||
| chr4:158845081
|
T | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-6240T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845081 | ||||||
| chr4:158845187
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-6134A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845187 | ||||||
| chr4:158845305
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.728-6016C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845305 | ||||||
| chr4:158845362
|
C | T | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-5959C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845362 | ||||||
| chr4:158845397
|
C | T | 10 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-5924C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845397 | ||||||
| chr4:158845445
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.728-5876T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845445 | ||||||
| chr4:158845633
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.728-5688A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845633 | ||||||
| chr4:158845834
|
T | C | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-5487T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845834 | ||||||
| chr4:158845938
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.728-5383G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158845938 | ||||||
| chr4:158846010
|
A | T | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-5311A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846010 | ||||||
| chr4:158846102
|
T | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-5219T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846102 | ||||||
| chr4:158846161
|
G | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.728-5160G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846161 | ||||||
| chr4:158846271
|
T | G | 7 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0008others(4): Show | 7 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-5050T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846271 | ||||||
| chr4:158846363
|
G | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.728-4958G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846363 | ||||||
| chr4:158846434
|
G | T | 1 | a0001c0001t0004g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-4887G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846434 | ||||||
| chr4:158846786
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-4535C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846786 | ||||||
| chr4:158846962
|
G | A | 1 | a0001c0001t0007g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-4359G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158846962 | ||||||
| chr4:158847032
|
G | C | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.728-4289G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847032 | ||||||
| chr4:158847074
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.728-4247G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847074 | ||||||
| chr4:158847232
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-4089G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847232 | ||||||
| chr4:158847458
|
C | G | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.728-3863C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847458 | ||||||
| chr4:158847877
|
C | T | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.728-3444C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847877 | ||||||
| chr4:158847909
|
C | T | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.728-3412C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847909 | ||||||
| chr4:158847943
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.728-3378A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158847943 | ||||||
| chr4:158848004
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.728-3317G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848004 | ||||||
| chr4:158848038
|
A | G | 10 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-3283A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848038 | ||||||
| chr4:158848805
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-2516C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848805 | ||||||
| chr4:158848953
|
G | C | 1 | a0001c0001t0005g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.728-2368G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848953 | ||||||
| chr4:158848961
|
A | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728-2360A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158848961 | ||||||
| chr4:158849133
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0008g0047 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.728-2188A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849133 | ||||||
| chr4:158849602
|
A | C | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728-1719A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849602 | ||||||
| chr4:158849605
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.728-1716G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849605 | ||||||
| chr4:158849904
|
T | C | 38 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0166others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.728-1417T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849904 | ||||||
| chr4:158849970
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.728-1351G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158849970 | ||||||
| chr4:158850293
|
T | C | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-1028T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850293 | ||||||
| chr4:158850317
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.728-1004T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850317 | ||||||
| chr4:158850488
|
T | C | 1 | a0001c0001t0009g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.728-833T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850488 | ||||||
| chr4:158850689
|
A | C | 4 | a0001c0003t0004g0016a0001c0003t0013g0027a0001c0003t0013g0028others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-632A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850689 | ||||||
| chr4:158850822
|
G | T | 1 | a0004c0006t0002g0247 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.728-499G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850822 | ||||||
| chr4:158850921
|
G | A | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.728-400G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850921 | ||||||
| chr4:158850934
|
C | T | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.728-387C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158850934 | ||||||
| chr4:158851180
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.728-141G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158851180 | ||||||
| chr4:158851201
|
T | C | 1 | a0001c0003t0017g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.728-120T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 7/16 | chr4 | 158851201 | ||||||
| chr4:158851490
|
G | C | 1 | a0001c0001t0019g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.857+40G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851490 | ||||||
| chr4:158851557
|
C | G | 3 | a0001c0001t0002g0204a0001c0001t0002g0209a0001c0001t0002g0249 | 3 | HG00280.hp2 HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.857+107C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851557 | ||||||
| chr4:158851627
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+177G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851627 | ||||||
| chr4:158851628
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+178C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851628 | ||||||
| chr4:158851688
|
T | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0059 | 2 | HG01081.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857+238T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851688 | ||||||
| chr4:158851704
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.857+254G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158851704 | ||||||
| chr4:158852062
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.857+612G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852062 | ||||||
| chr4:158852360
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+910T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852360 | ||||||
| chr4:158852453
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.857+1003A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852453 | ||||||
| chr4:158852550
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+1100G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158852550 | ||||||
| chr4:158853110
|
CATA | C | 37 | a0002c0002t0003g0104a0002c0002t0003g0166a0002c0002t0003g0167others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.857+1664_857+1666d others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158853110 | |||||
| chr4:158853208
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+1758G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853208 | ||||||
| chr4:158853329
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(1): Show | 4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+1879G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853329 | ||||||
| chr4:158853419
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.857+1969C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853419 | ||||||
| chr4:158853504
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.857+2054C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853504 | ||||||
| chr4:158853833
|
A | G | 2 | a0001c0001t0002g0212a0001c0001t0002g0217 | 2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.857+2383A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158853833 | ||||||
| chr4:158854090
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+2640T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854090 | ||||||
| chr4:158854286
|
C | CTGGCCTC others(3): Show |
1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.857+2837_857+2846d others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158854286 | |||||
| chr4:158854449
|
T | G | 117 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(114): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.857+2999T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854449 | ||||||
| chr4:158854521
|
G | A | 38 | a0002c0002t0003g0025a0002c0002t0003g0104a0002c0002t0003g0166others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.857+3071G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854521 | ||||||
| chr4:158854876
|
G | A | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.857+3426G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158854876 | ||||||
| chr4:158855000
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.857+3550C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855000 | ||||||
| chr4:158855008
|
T | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.857+3558T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855008 | ||||||
| chr4:158855123
|
T | C | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 29 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.857+3673T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855123 | ||||||
| chr4:158855212
|
G | A | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.857+3762G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855212 | ||||||
| chr4:158855446
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.858-3611G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855446 | ||||||
| chr4:158855851
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.858-3206C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855851 | ||||||
| chr4:158855984
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.858-3073C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158855984 | ||||||
| chr4:158856038
|
C | T | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.858-3019C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856038 | ||||||
| chr4:158856371
|
T | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-2686T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856371 | ||||||
| chr4:158856438
|
A | C | 98 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(95): Show | 99 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.858-2619A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856438 | ||||||
| chr4:158856444
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858-2613G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856444 | ||||||
| chr4:158856612
|
A | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.858-2445A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856612 | ||||||
| chr4:158856718
|
A | T | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-2339A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856718 | ||||||
| chr4:158856953
|
T | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-2104T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856953 | ||||||
| chr4:158856969
|
G | A | 2 | a0001c0001t0002g0240a0001c0001t0002g0241 | 2 | NA18963.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.858-2088G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158856969 | ||||||
| chr4:158857092
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.858-1965G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857092 | ||||||
| chr4:158857332
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.858-1725G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857332 | ||||||
| chr4:158857647
|
T | C | 1 | a0002c0002t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1410T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857647 | ||||||
| chr4:158857650
|
A | T | 1 | a0002c0002t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1407A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857650 | ||||||
| chr4:158857663
|
C | G | 1 | a0002c0002t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.858-1394C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857663 | ||||||
| chr4:158857693
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858-1364A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857693 | ||||||
| chr4:158857771
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858-1286C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857771 | ||||||
| chr4:158857780
|
C | CA | 106 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(103): Show | 106 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.858-1260dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | |||||
| chr4:158857780
|
CA | C | 55 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0204others(52): Show | 56 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.858-1260delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | |||||
| chr4:158857780
|
CAAAAAAA others(1): Show |
C | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-1267_858-1260d others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 158857780 | |||||
| chr4:158857785
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.858-1272A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857785 | ||||||
| chr4:158857946
|
C | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0079others(9): Show | 12 | HG01081.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.858-1111C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857946 | ||||||
| chr4:158857975
|
C | T | 1 | a0001c0001t0005g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.858-1082C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857975 | ||||||
| chr4:158857986
|
A | G | 1 | a0001c0003t0004g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.858-1071A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158857986 | ||||||
| chr4:158858017
|
T | C | 1 | a0001c0001t0015g0097 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.858-1040T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858017 | ||||||
| chr4:158858042
|
T | C | 117 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(114): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.858-1015T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858042 | ||||||
| chr4:158858089
|
G | A | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 29 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.858-968G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858089 | ||||||
| chr4:158858109
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.858-948T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858109 | ||||||
| chr4:158858112
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.858-945T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858112 | ||||||
| chr4:158858156
|
A | G | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.858-901A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858156 | ||||||
| chr4:158858660
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-397C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 8/16 | chr4 | 158858660 | ||||||
| chr4:158859516
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1060-62G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 9/16 | chr4 | 158859516 | ||||||
| chr4:158859696
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1148+30A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859696 | ||||||
| chr4:158859838
|
C | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1148+172C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859838 | ||||||
| chr4:158859854
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1148+188C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158859854 | ||||||
| chr4:158860418
|
C | CT | 35 | a0002c0002t0003g0025a0002c0002t0003g0104a0002c0002t0003g0166others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1148+760dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 158860418 | |||||
| chr4:158860470
|
T | C | 1 | a0001c0001t0005g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1148+804T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860470 | ||||||
| chr4:158860549
|
T | C | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1149-793T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860549 | ||||||
| chr4:158860654
|
C | CT | 64 | a0001c0001t0001g0075a0001c0001t0001g0253a0001c0001t0002g0001others(61): Show | 65 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1149-666dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 158860654 | |||||
| chr4:158860689
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149-653G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860689 | ||||||
| chr4:158860798
|
A | C | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-544A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860798 | ||||||
| chr4:158860799
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-543G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860799 | ||||||
| chr4:158860800
|
G | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-542G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860800 | ||||||
| chr4:158860801
|
C | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1149-541C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860801 | ||||||
| chr4:158860857
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-485A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158860857 | ||||||
| chr4:158861001
|
A | G | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1149-341A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158861001 | ||||||
| chr4:158861128
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1149-214C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 10/16 | chr4 | 158861128 | ||||||
| chr4:158861858
|
C | G | 17 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1465+82C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158861858 | ||||||
| chr4:158862003
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1465+227A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862003 | ||||||
| chr4:158862087
|
T | C | 1 | a0001c0003t0004g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1465+311T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862087 | ||||||
| chr4:158862497
|
A | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1465+721A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862497 | ||||||
| chr4:158862819
|
T | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.1465+1043T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862819 | ||||||
| chr4:158862956
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1465+1180T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158862956 | ||||||
| chr4:158863217
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1465+1441C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863217 | ||||||
| chr4:158863218
|
G | A | 1 | a0001c0009t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1465+1442G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863218 | ||||||
| chr4:158863243
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+1467G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863243 | ||||||
| chr4:158863304
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1465+1528G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863304 | ||||||
| chr4:158863343
|
C | T | 38 | a0001c0001t0003g0184a0002c0002t0003g0104a0002c0002t0003g0166others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1465+1567C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863343 | ||||||
| chr4:158863376
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1465+1600A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863376 | ||||||
| chr4:158863509
|
C | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1465+1733C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863509 | ||||||
| chr4:158863594
|
G | A | 6 | a0002c0002t0003g0025a0002c0002t0003g0167a0002c0002t0003g0171others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465+1818G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158863594 | ||||||
| chr4:158863810
|
TC | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(46): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1465+2036delC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158863810 | |||||
| chr4:158864183
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2407G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864183 | ||||||
| chr4:158864250
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1465+2474T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864250 | ||||||
| chr4:158864266
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2490C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864266 | ||||||
| chr4:158864267
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1465+2491G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864267 | ||||||
| chr4:158864361
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465+2585C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864361 | ||||||
| chr4:158864365
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG02129.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1465+2589T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864365 | ||||||
| chr4:158864377
|
AATT | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(2): Show | 5 | HG03471.hp2 HG04228.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465+2603_1465+260 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158864377 | |||||
| chr4:158864590
|
A | G | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1465+2814A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864590 | ||||||
| chr4:158864786
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1465+3010A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864786 | ||||||
| chr4:158864835
|
C | T | 16 | a0001c0003t0004g0018a0001c0003t0004g0019a0001c0003t0004g0020others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+3059C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864835 | ||||||
| chr4:158864955
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-3147C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158864955 | ||||||
| chr4:158865039
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0043others(63): Show | 66 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1466-3063C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865039 | ||||||
| chr4:158865105
|
G | A | 4 | a0001c0003t0004g0024a0001c0003t0004g0125a0001c0003t0004g0126others(1): Show | 4 | HG00609.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1466-2997G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865105 | ||||||
| chr4:158865458
|
A | G | 1 | a0001c0001t0018g0124 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1466-2644A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865458 | ||||||
| chr4:158865627
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1466-2475G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865627 | ||||||
| chr4:158865686
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-2416C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865686 | ||||||
| chr4:158865992
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-2110C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158865992 | ||||||
| chr4:158866065
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1466-2037A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866065 | ||||||
| chr4:158866221
|
C | CTTTTTTT others(3): Show |
55 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(52): Show | 55 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1466-1875_1466-186 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | |||||
| chr4:158866221
|
C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0146others(11): Show | 14 | HG01257.hp2 HG01891.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1466-1876_1466-186 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | |||||
| chr4:158866221
|
C | CTTTTTTT others(5): Show |
133 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(130): Show | 134 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1466-1877_1466-186 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | |||||
| chr4:158866221
|
C | CTTTTTTT others(6): Show |
36 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0058others(33): Show | 36 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1466-1878_1466-186 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | |||||
| chr4:158866221
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0130a0001c0001t0002g0223a0001c0001t0009g0231 | 3 | HG01192.hp2 HG02300.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1466-1879_1466-186 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr4 | 158866221 | |||||
| chr4:158866221
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1466-1881C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866221 | ||||||
| chr4:158866305
|
G | A | 1 | a0004c0006t0002g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1466-1797G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866305 | ||||||
| chr4:158866322
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-1780G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866322 | ||||||
| chr4:158866416
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(1): Show | 4 | HG04228.hp1 NA18986.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466-1686C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866416 | ||||||
| chr4:158866507
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1466-1595C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866507 | ||||||
| chr4:158866584
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1466-1518T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866584 | ||||||
| chr4:158866736
|
TGGCTAAT others(54): Show |
T | 1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-1365_1466-130 others(65): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866736 | ||||||
| chr4:158866877
|
G | A | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(12): Show | 15 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1466-1225G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866877 | ||||||
| chr4:158866947
|
C | T | 1 | a0001c0003t0004g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1466-1155C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158866947 | ||||||
| chr4:158867212
|
A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1466-890A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867212 | ||||||
| chr4:158867453
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1466-649A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867453 | ||||||
| chr4:158867455
|
G | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1466-647G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867455 | ||||||
| chr4:158867602
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1466-500G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867602 | ||||||
| chr4:158867698
|
A | G | 38 | a0002c0002t0003g0025a0002c0002t0003g0104a0002c0002t0003g0166others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1466-404A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867698 | ||||||
| chr4:158867714
|
C | G | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0009t0002g0234others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1466-388C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867714 | ||||||
| chr4:158867779
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1466-323C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867779 | ||||||
| chr4:158867838
|
C | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1466-264C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867838 | ||||||
| chr4:158867848
|
A | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1466-254A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158867848 | ||||||
| chr4:158868016
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466-86A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868016 | ||||||
| chr4:158868045
|
A | C | 1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-57A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868045 | ||||||
| chr4:158868047
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1466-55C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 12/16 | chr4 | 158868047 | ||||||
| chr4:158869717
|
G | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2792+289G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 13/16 | chr4 | 158869717 | ||||||
| chr4:158870737
|
T | G | 1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2949+268T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870737 | ||||||
| chr4:158870828
|
G | A | 1 | a0001c0001t0008g0120 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2949+359G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870828 | ||||||
| chr4:158870880
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2949+411G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870880 | ||||||
| chr4:158870919
|
C | T | 1 | a0002c0002t0003g0197 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2949+450C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158870919 | ||||||
| chr4:158871178
|
G | A | 1 | a0001c0001t0009g0144 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2949+709G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871178 | ||||||
| chr4:158871478
|
C | A | 1 | a0001c0001t0002g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2949+1009C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871478 | ||||||
| chr4:158871478
|
C | T | 56 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(53): Show | 57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2949+1009C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871478 | ||||||
| chr4:158871557
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2949+1088A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871557 | ||||||
| chr4:158871831
|
C | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2949+1362C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158871831 | ||||||
| chr4:158872490
|
C | T | 1 | a0008c0012t0002g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2949+2021C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872490 | ||||||
| chr4:158872734
|
G | GT | 16 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0090others(13): Show | 16 | HG01981.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2949+2282dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158872734 | |||||
| chr4:158872736
|
T | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+2267T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872736 | ||||||
| chr4:158872741
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2949+2272T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872741 | ||||||
| chr4:158872743
|
T | TG | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2949+2274_2949+227 others(5): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872743 | ||||||
| chr4:158872745
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2949+2276T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872745 | ||||||
| chr4:158872751
|
TA | T | 9 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0001g0114others(6): Show | 9 | HG01169.hp1 HG01257.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2949+2288delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158872751 | |||||
| chr4:158872752
|
A | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 239 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.2949+2283A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872752 | ||||||
| chr4:158872753
|
A | T | 15 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(12): Show | 15 | HG00558.hp2 HG02083.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+2284A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872753 | ||||||
| chr4:158872983
|
A | G | 6 | a0002c0002t0003g0104a0002c0002t0003g0173a0002c0002t0003g0174others(3): Show | 6 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2949+2514A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158872983 | ||||||
| chr4:158873032
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2949+2563C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873032 | ||||||
| chr4:158873156
|
AAAG | A | 10 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+2690_2949+269 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158873156 | |||||
| chr4:158873636
|
T | C | 1 | a0001c0001t0002g0001 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2949+3167T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873636 | ||||||
| chr4:158873824
|
T | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+3355T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873824 | ||||||
| chr4:158873908
|
G | A | 1 | a0003c0004t0001g0150 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2949+3439G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873908 | ||||||
| chr4:158873928
|
G | T | 1 | a0001c0001t0002g0226 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2949+3459G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158873928 | ||||||
| chr4:158874492
|
C | CAAAAAAA others(2): Show |
43 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0079others(40): Show | 43 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2949+4028_2949+403 others(13): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | |||||
| chr4:158874492
|
C | CAAAAAAA others(3): Show |
113 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0039others(110): Show | 113 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.2949+4027_2949+403 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | |||||
| chr4:158874492
|
C | CAAAAAAA others(4): Show |
84 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0045others(81): Show | 85 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.2949+4026_2949+403 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | |||||
| chr4:158874492
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0218a0001c0001t0012g0088 | 2 | HG02145.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2949+4025_2949+403 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | |||||
| chr4:158874492
|
C | CAAAAAAA others(6): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+4024_2949+403 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874492 | |||||
| chr4:158874579
|
A | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2949+4110A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874579 | ||||||
| chr4:158874593
|
C | G | 1 | a0011c0013t0008g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2949+4124C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874593 | ||||||
| chr4:158874790
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+4321A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158874790 | ||||||
| chr4:158874923
|
CA | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(246): Show | 250 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.2949+4468delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158874923 | |||||
| chr4:158875086
|
C | CA | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0065others(5): Show | 8 | HG00423.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2949+4632dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875086 | |||||
| chr4:158875091
|
A | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4622A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875091 | ||||||
| chr4:158875098
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0005g0009 | 2 | HG03486.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2949+4629A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875098 | ||||||
| chr4:158875159
|
C | G | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4690C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875159 | ||||||
| chr4:158875412
|
C | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2949+4943C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875412 | ||||||
| chr4:158875515
|
G | GATATAT | 57 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(54): Show | 57 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.2949+5067_2949+507 others(10): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(1): Show |
36 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0043others(33): Show | 36 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2949+5065_2949+507 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(3): Show |
9 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0135others(6): Show | 9 | HG00423.hp1 HG00609.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2949+5063_2949+507 others(14): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(5): Show |
7 | a0001c0001t0001g0066a0001c0001t0001g0084a0002c0002t0007g0169others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+5061_2949+507 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(7): Show |
10 | a0002c0002t0003g0104a0002c0002t0003g0174a0002c0002t0003g0178others(7): Show | 10 | HG00438.hp2 HG02080.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5059_2949+507 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(9): Show |
10 | a0001c0001t0003g0184a0001c0001t0004g0136a0001c0001t0012g0089others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5057_2949+507 others(20): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(11): Show |
10 | a0001c0001t0012g0088a0001c0003t0004g0019a0001c0003t0004g0022others(7): Show | 10 | HG00280.hp1 HG01943.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2949+5055_2949+507 others(22): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(13): Show |
15 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0073others(12): Show | 15 | HG00438.hp1 HG00738.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2949+5053_2949+507 others(24): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(15): Show |
6 | a0001c0001t0001g0087a0001c0001t0005g0007a0001c0001t0005g0008others(3): Show | 6 | HG02922.hp1 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2949+5051_2949+507 others(26): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(17): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0005g0159others(4): Show | 7 | HG01981.hp2 HG02135.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2949+5049_2949+507 others(28): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(19): Show |
7 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0145others(4): Show | 7 | HG00423.hp2 HG00609.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+5047_2949+507 others(30): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(21): Show |
3 | a0001c0003t0013g0027a0002c0002t0003g0192a0010c0015t0004g0013 | 3 | HG02615.hp2 HG02965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(32): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(23): Show |
3 | a0001c0001t0003g0036a0003c0004t0001g0056a0003c0004t0001g0149 | 3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(34): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(25): Show |
3 | a0001c0001t0005g0010a0002c0002t0003g0201a0003c0004t0001g0054 | 3 | HG01169.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(27): Show |
1 | a0002c0002t0004g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(38): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(29): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0146others(1): Show | 4 | HG02109.hp2 HG03471.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(40): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(31): Show |
3 | a0001c0003t0017g0017a0002c0002t0003g0173a0003c0004t0001g0053 | 3 | HG00558.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(42): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(33): Show |
4 | a0001c0003t0004g0016a0002c0002t0003g0167a0003c0004t0001g0148others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
G | GATATATA others(39): Show |
1 | a0001c0003t0013g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(50): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
GATATATA others(1): Show |
G | 48 | a0001c0001t0001g0041a0001c0001t0002g0001a0001c0001t0002g0202others(45): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2949+5065_2949+507 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875515
|
GATATATA others(7): Show |
G | 2 | a0001c0001t0007g0031a0001c0001t0007g0032 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2949+5059_2949+507 others(18): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158875515 | |||||
| chr4:158875540
|
A | G | 45 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(42): Show | 46 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2949+5071A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875540 | ||||||
| chr4:158875541
|
T | C | 45 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(42): Show | 46 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2949+5072T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | ||||||
| chr4:158875541
|
T | TATATATA others(41): Show |
1 | a0009c0016t0002g0236 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(52): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | ||||||
| chr4:158875541
|
T | TATATATA others(39): Show |
2 | a0001c0001t0002g0233a0001c0009t0002g0235 | 2 | HG00735.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2949+5072_2949+507 others(50): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | ||||||
| chr4:158875541
|
T | TATATATA others(25): Show |
1 | a0001c0009t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | ||||||
| chr4:158875541
|
T | TATATATA others(23): Show |
1 | a0001c0001t0002g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2949+5072_2949+507 others(34): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875541 | ||||||
| chr4:158875542
|
G | A | 38 | a0001c0001t0003g0184a0002c0002t0003g0104a0002c0002t0003g0166others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.2949+5073G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875542 | ||||||
| chr4:158875704
|
T | A | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2949+5235T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875704 | ||||||
| chr4:158875890
|
A | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5421A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158875890 | ||||||
| chr4:158876010
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+5541C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876010 | ||||||
| chr4:158876063
|
A | G | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+5594A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876063 | ||||||
| chr4:158876174
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2949+5705C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876174 | ||||||
| chr4:158876245
|
T | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0079others(9): Show | 12 | HG01081.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2949+5776T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876245 | ||||||
| chr4:158876463
|
A | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0112others(7): Show | 10 | HG00621.hp1 HG02080.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.2949+5994A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876463 | ||||||
| chr4:158876507
|
C | T | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2949+6038C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876507 | ||||||
| chr4:158876773
|
A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2949+6304A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876773 | ||||||
| chr4:158876994
|
C | T | 6 | a0002c0002t0003g0166a0002c0002t0003g0185a0002c0002t0003g0186others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2949+6525C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158876994 | ||||||
| chr4:158877010
|
A | G | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2949+6541A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877010 | ||||||
| chr4:158877265
|
C | T | 5 | a0001c0005t0002g0211a0001c0005t0002g0213a0001c0005t0002g0215others(2): Show | 5 | HG02735.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2949+6796C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877265 | ||||||
| chr4:158877310
|
C | A | 1 | a0007c0011t0005g0004 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2949+6841C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877310 | ||||||
| chr4:158877386
|
A | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(55): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2949+6917A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877386 | ||||||
| chr4:158877531
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2949+7062G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877531 | ||||||
| chr4:158877803
|
A | G | 115 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(112): Show | 116 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2949+7334A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877803 | ||||||
| chr4:158877883
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2949+7414T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877883 | ||||||
| chr4:158877934
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2949+7465C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158877934 | ||||||
| chr4:158878191
|
G | T | 1 | a0001c0001t0002g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2949+7722G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878191 | ||||||
| chr4:158878536
|
A | G | 1 | a0002c0002t0003g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2949+8067A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878536 | ||||||
| chr4:158878790
|
C | T | 52 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(49): Show | 53 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2949+8321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878790 | ||||||
| chr4:158878862
|
TGTAAGAA others(1290): Show |
T | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+8394_2949+969 others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878862 | ||||||
| chr4:158878999
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2949+8530T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158878999 | ||||||
| chr4:158879081
|
A | G | 2 | a0003c0004t0001g0053a0003c0004t0001g0056 | 2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2949+8612A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879081 | ||||||
| chr4:158879640
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2949+9171A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879640 | ||||||
| chr4:158879923
|
A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2949+9454A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158879923 | ||||||
| chr4:158880139
|
C | G | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2949+9670C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880139 | ||||||
| chr4:158880160
|
A | T | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9691A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880160 | ||||||
| chr4:158880166
|
C | T | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9697C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880166 | ||||||
| chr4:158880174
|
C | T | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9705C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880174 | ||||||
| chr4:158880193
|
C | G | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9724C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880193 | ||||||
| chr4:158880207
|
T | G | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9738T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880207 | ||||||
| chr4:158880208
|
A | G | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9739A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880208 | ||||||
| chr4:158880220
|
T | A | 35 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(32): Show | 35 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.2949+9751T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880220 | ||||||
| chr4:158880332
|
C | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098 | 3 | HG00621.hp2 NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2949+9863C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880332 | ||||||
| chr4:158880813
|
A | G | 1 | a0001c0007t0006g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2949+10344A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880813 | ||||||
| chr4:158880877
|
G | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+10408G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880877 | ||||||
| chr4:158880959
|
A | G | 57 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(54): Show | 58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-10487A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880959 | ||||||
| chr4:158880996
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2950-10450C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158880996 | ||||||
| chr4:158881115
|
C | T | 18 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0052others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.2950-10331C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881115 | ||||||
| chr4:158881190
|
CTCCACGG others(18): Show |
C | 7 | a0001c0001t0003g0036a0001c0001t0007g0031a0001c0001t0007g0032others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950-10199_2950-10 others(31): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881190 | |||||
| chr4:158881211
|
C | G | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-10235C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881211 | ||||||
| chr4:158881221
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.2950-10225G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881221 | ||||||
| chr4:158881247
|
G | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-10199G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881247 | ||||||
| chr4:158881272
|
T | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10174T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881272 | ||||||
| chr4:158881287
|
T | TCTTTCCA others(12): Show |
8 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(5): Show | 8 | HG01884.hp1 HG01981.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-10156_2950-10 others(25): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881287 | |||||
| chr4:158881296
|
GGTCTCCC others(23): Show |
G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10140_2950-10 others(36): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881296 | |||||
| chr4:158881322
|
G | A | 19 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0098others(16): Show | 19 | HG00609.hp2 HG00621.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2950-10124G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881322 | ||||||
| chr4:158881326
|
C | CGTCTCCC others(18): Show |
2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-10076_2950-10 others(31): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881326 | |||||
| chr4:158881327
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-10119G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881327 | ||||||
| chr4:158881327
|
G | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10119G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881327 | ||||||
| chr4:158881361
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10085T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881361 | ||||||
| chr4:158881363
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10083C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881363 | ||||||
| chr4:158881376
|
G | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10070G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881376 | ||||||
| chr4:158881380
|
TC | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10063delC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881380 | |||||
| chr4:158881383
|
C | G | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10063C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881383 | ||||||
| chr4:158881393
|
C | T | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-10053C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881393 | ||||||
| chr4:158881394
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10052T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881394 | ||||||
| chr4:158881394
|
TCTCTCTT others(18): Show |
T | 240 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(237): Show | 241 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.2950-9978_2950-995 others(29): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881394 | |||||
| chr4:158881394
|
TCTCTCTT others(43): Show |
T | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2950-10003_2950-99 others(55): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881394 | |||||
| chr4:158881444
|
C | CCTCTCT | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063 | 3 | HG00597.hp1 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2950-10001_2950-99 others(11): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881444 | |||||
| chr4:158881481
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2950-9965C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881481 | ||||||
| chr4:158881509
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9937T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881509 | ||||||
| chr4:158881513
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2950-9933C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881513 | ||||||
| chr4:158881535
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2950-9911C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881535 | ||||||
| chr4:158881546
|
CCCTGCCT others(6): Show |
C | 195 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(192): Show | 195 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.2950-9892_2950-988 others(17): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881546 | |||||
| chr4:158881561
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0008g0092 | 2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2950-9885C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881561 | ||||||
| chr4:158881626
|
T | A | 3 | a0001c0001t0004g0136a0001c0001t0012g0088a0001c0001t0012g0089 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2950-9820T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881626 | ||||||
| chr4:158881660
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2950-9786C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881660 | ||||||
| chr4:158881685
|
G | A | 1 | a0001c0001t0019g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2950-9761G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881685 | ||||||
| chr4:158881712
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950-9734C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881712 | ||||||
| chr4:158881783
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0073others(5): Show | 8 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2950-9663C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881783 | ||||||
| chr4:158881871
|
A | AC | 9 | a0001c0001t0001g0039a0001c0001t0001g0116a0001c0001t0002g0218others(6): Show | 9 | HG02145.hp2 HG02602.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-9571dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158881871 | |||||
| chr4:158881983
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2950-9463C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158881983 | ||||||
| chr4:158882059
|
T | G | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.2950-9387T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882059 | ||||||
| chr4:158882187
|
A | AGCAGCCG others(33): Show |
1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9220_2950-918 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882187 | |||||
| chr4:158882187
|
AGCAGCCG others(33): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2950-9220_2950-918 others(44): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882187 | |||||
| chr4:158882193
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0006c0010t0001g0128 | 3 | HG01517.hp2 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2950-9253C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882193 | ||||||
| chr4:158882197
|
C | G | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-9249C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882197 | ||||||
| chr4:158882226
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(14): Show | 17 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.2950-9220C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882226 | ||||||
| chr4:158882233
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2950-9213C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882233 | ||||||
| chr4:158882239
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2950-9207G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882239 | ||||||
| chr4:158882266
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9180T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882266 | ||||||
| chr4:158882274
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9172A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882274 | ||||||
| chr4:158882297
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2950-9149G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882297 | ||||||
| chr4:158882309
|
C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9137C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882309 | ||||||
| chr4:158882365
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-9081G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882365 | ||||||
| chr4:158882396
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2950-9050C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882396 | ||||||
| chr4:158882413
|
G | A | 1 | a0002c0002t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2950-9033G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882413 | ||||||
| chr4:158882481
|
A | AC | 69 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0050others(66): Show | 69 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.2950-8961dupC | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158882481 | |||||
| chr4:158882532
|
C | T | 1 | a0001c0001t0018g0124 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2950-8914C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882532 | ||||||
| chr4:158882548
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8898G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882548 | ||||||
| chr4:158882568
|
C | T | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-8878C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882568 | ||||||
| chr4:158882653
|
G | C | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2950-8793G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882653 | ||||||
| chr4:158882787
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0002g0226 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2950-8659G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882787 | ||||||
| chr4:158882800
|
A | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0032a0002c0002t0007g0169others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-8646A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882800 | ||||||
| chr4:158882856
|
C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8590C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882856 | ||||||
| chr4:158882859
|
C | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8587C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882859 | ||||||
| chr4:158882867
|
C | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0032a0002c0002t0007g0169others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-8579C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882867 | ||||||
| chr4:158882976
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-8470C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158882976 | ||||||
| chr4:158883113
|
A | C | 61 | a0001c0001t0001g0095a0001c0001t0001g0106a0001c0001t0001g0108others(58): Show | 62 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2950-8333A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883113 | ||||||
| chr4:158883115
|
A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-8331A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883115 | ||||||
| chr4:158883146
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0067 | 2 | HG02129.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2950-8300A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883146 | ||||||
| chr4:158883238
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2950-8208T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883238 | ||||||
| chr4:158883243
|
G | GT | 48 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(45): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2950-8195dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883243 | |||||
| chr4:158883320
|
C | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0087 | 2 | HG02257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2950-8126C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883320 | ||||||
| chr4:158883334
|
T | C | 1 | a0002c0002t0003g0194 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2950-8112T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883334 | ||||||
| chr4:158883342
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2950-8104C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883342 | ||||||
| chr4:158883387
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2950-8059G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883387 | ||||||
| chr4:158883429
|
G | A | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2950-8017G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883429 | ||||||
| chr4:158883431
|
C | T | 5 | a0001c0001t0002g0237a0001c0001t0002g0240a0001c0001t0002g0241others(2): Show | 5 | HG01934.hp1 NA18955.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950-8015C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883431 | ||||||
| chr4:158883521
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2950-7925G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883521 | ||||||
| chr4:158883529
|
T | C | 117 | a0001c0001t0001g0137a0001c0001t0002g0001a0001c0001t0002g0202others(114): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2950-7917T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883529 | ||||||
| chr4:158883587
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2950-7859T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883587 | ||||||
| chr4:158883802
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2950-7644A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158883802 | ||||||
| chr4:158883949
|
CT | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 203 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.2950-7477delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883949 | |||||
| chr4:158883949
|
CTT | C | 36 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(33): Show | 36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.2950-7478_2950-747 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158883949 | |||||
| chr4:158884218
|
T | G | 57 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(54): Show | 58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-7228T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884218 | ||||||
| chr4:158884424
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-7022A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884424 | ||||||
| chr4:158884495
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2950-6951G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884495 | ||||||
| chr4:158884723
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-6723G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884723 | ||||||
| chr4:158884733
|
G | C | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2950-6713G>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884733 | ||||||
| chr4:158884762
|
G | A | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-6684G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884762 | ||||||
| chr4:158884858
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2950-6588C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158884858 | ||||||
| chr4:158884978
|
T | TA | 10 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0099others(7): Show | 10 | HG01192.hp1 HG01192.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2950-6448dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158884978 | |||||
| chr4:158884978
|
TA | T | 56 | a0001c0001t0001g0066a0001c0001t0002g0001a0001c0001t0002g0202others(53): Show | 57 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2950-6448delA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158884978 | |||||
| chr4:158885000
|
A | T | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2950-6446A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885000 | ||||||
| chr4:158885037
|
T | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2950-6409T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885037 | ||||||
| chr4:158885594
|
G | T | 1 | a0002c0002t0003g0178 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2950-5852G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885594 | ||||||
| chr4:158885651
|
G | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-5795G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885651 | ||||||
| chr4:158885658
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2950-5788C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885658 | ||||||
| chr4:158885810
|
C | G | 4 | a0001c0001t0007g0031a0001c0001t0007g0032a0002c0002t0007g0169others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-5636C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158885810 | ||||||
| chr4:158886051
|
C | G | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0063others(5): Show | 8 | HG00597.hp1 HG01192.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.2950-5395C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886051 | ||||||
| chr4:158886456
|
T | G | 34 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-4990T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886456 | ||||||
| chr4:158886511
|
C | A | 18 | a0001c0001t0003g0036a0001c0003t0004g0016a0001c0003t0004g0018others(15): Show | 18 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.2950-4935C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886511 | ||||||
| chr4:158886526
|
C | G | 34 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-4920C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886526 | ||||||
| chr4:158886860
|
A | G | 6 | a0001c0001t0003g0036a0001c0001t0007g0031a0001c0001t0007g0032others(3): Show | 6 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2950-4586A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158886860 | ||||||
| chr4:158887047
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2950-4399C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887047 | ||||||
| chr4:158887064
|
G | T | 8 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(5): Show | 8 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-4382G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887064 | ||||||
| chr4:158887084
|
A | G | 1 | a0002c0002t0007g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2950-4362A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887084 | ||||||
| chr4:158887631
|
G | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0032a0002c0002t0007g0169others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-3815G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887631 | ||||||
| chr4:158887736
|
C | CA | 5 | a0001c0001t0002g0241a0001c0001t0005g0006a0001c0008t0010g0033others(2): Show | 5 | HG01169.hp2 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950-3689dupA | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | |||||
| chr4:158887736
|
C | CAA | 177 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0039others(174): Show | 178 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.2950-3690_2950-368 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | |||||
| chr4:158887736
|
C | CAAA | 46 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0045others(43): Show | 46 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2950-3691_2950-368 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | |||||
| chr4:158887736
|
C | CAAAA | 9 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(6): Show | 9 | HG00609.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-3692_2950-368 others(8): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | |||||
| chr4:158887736
|
C | CAAAAA | 7 | a0001c0003t0004g0020a0001c0003t0004g0021a0001c0003t0004g0022others(4): Show | 7 | HG02055.hp1 HG02135.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2950-3693_2950-368 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158887736 | |||||
| chr4:158887758
|
C | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-3688C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158887758 | ||||||
| chr4:158888228
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2950-3218G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888228 | ||||||
| chr4:158888288
|
T | C | 10 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2950-3158T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888288 | ||||||
| chr4:158888346
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(240): Show | 244 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.2950-3100A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888346 | ||||||
| chr4:158888404
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2950-3042A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888404 | ||||||
| chr4:158888432
|
C | T | 1 | a0006c0010t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2950-3014C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888432 | ||||||
| chr4:158888643
|
T | G | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2950-2803T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888643 | ||||||
| chr4:158888830
|
C | T | 54 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(51): Show | 55 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2950-2616C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888830 | ||||||
| chr4:158888853
|
G | A | 1 | a0001c0003t0004g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2950-2593G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158888853 | ||||||
| chr4:158888875
|
CAAAAAAA others(1): Show |
C | 34 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.2950-2561_2950-255 others(12): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158888875 | |||||
| chr4:158889237
|
AT | A | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950-2203delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158889237 | |||||
| chr4:158889263
|
A | G | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2950-2183A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889263 | ||||||
| chr4:158889325
|
T | A | 1 | a0001c0001t0007g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2950-2121T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889325 | ||||||
| chr4:158889489
|
C | A | 5 | a0002c0002t0003g0179a0002c0002t0003g0190a0002c0002t0003g0191others(2): Show | 5 | HG00423.hp2 NA18966.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.2950-1957C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889489 | ||||||
| chr4:158889566
|
C | A | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-1880C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889566 | ||||||
| chr4:158889619
|
A | T | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2950-1827A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889619 | ||||||
| chr4:158889638
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2950-1808A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158889638 | ||||||
| chr4:158889805
|
CT | C | 57 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(54): Show | 58 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2950-1627delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 158889805 | |||||
| chr4:158890633
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2950-813T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890633 | ||||||
| chr4:158890767
|
G | T | 2 | a0002c0002t0004g0037a0002c0002t0004g0038 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-679G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890767 | ||||||
| chr4:158890959
|
C | T | 3 | a0001c0001t0007g0032a0002c0002t0007g0169a0002c0002t0007g0170 | 3 | HG02559.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2950-487C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158890959 | ||||||
| chr4:158891149
|
T | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2950-297T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891149 | ||||||
| chr4:158891158
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2950-288T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891158 | ||||||
| chr4:158891192
|
C | G | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0009t0002g0234others(2): Show | 5 | HG00735.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2950-254C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891192 | ||||||
| chr4:158891247
|
C | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.2950-199C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 14/16 | chr4 | 158891247 | ||||||
| chr4:158891794
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3150+148C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158891794 | ||||||
| chr4:158891830
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00621.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.3150+184G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158891830 | ||||||
| chr4:158892047
|
G | A | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+401G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892047 | ||||||
| chr4:158892141
|
C | CT | 11 | a0001c0001t0001g0087a0001c0001t0001g0106a0001c0001t0001g0138others(8): Show | 11 | HG01891.hp2 HG02135.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3150+516dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892141 | |||||
| chr4:158892141
|
CT | C | 52 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0002g0001others(49): Show | 53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3150+516delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892141 | |||||
| chr4:158892412
|
G | A | 6 | a0001c0001t0003g0036a0001c0001t0007g0031a0001c0001t0007g0032others(3): Show | 6 | HG02559.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+766G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892412 | ||||||
| chr4:158892552
|
A | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3150+906A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892552 | ||||||
| chr4:158892622
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+976C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892622 | ||||||
| chr4:158892624
|
C | G | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3150+978C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892624 | ||||||
| chr4:158892666
|
C | G | 1 | a0010c0015t0004g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3150+1020C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158892666 | ||||||
| chr4:158892945
|
AAG | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG00735.hp1 HG01081.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.3150+1302_3150+130 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158892945 | |||||
| chr4:158893099
|
A | C | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3150+1453A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893099 | ||||||
| chr4:158893277
|
T | C | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3150+1631T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893277 | ||||||
| chr4:158893481
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0110 | 2 | NA18982.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3150+1835A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893481 | ||||||
| chr4:158893626
|
T | TATGATCT others(369): Show |
1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3150+1995_3150+199 others(380): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158893626 | |||||
| chr4:158893702
|
G | A | 1 | a0002c0002t0003g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3151-2048G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893702 | ||||||
| chr4:158893891
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3151-1859A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158893891 | ||||||
| chr4:158894170
|
C | CT | 17 | a0001c0001t0007g0031a0001c0003t0004g0016a0001c0003t0004g0019others(14): Show | 17 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.3151-1562dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158894170 | |||||
| chr4:158894170
|
CT | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0039others(107): Show | 110 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.3151-1562delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 158894170 | |||||
| chr4:158894418
|
T | C | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3151-1332T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894418 | ||||||
| chr4:158894604
|
G | A | 1 | a0002c0017t0003g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3151-1146G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894604 | ||||||
| chr4:158894727
|
G | A | 3 | a0001c0003t0004g0125a0001c0003t0004g0126a0001c0003t0004g0134 | 3 | HG00609.hp2 HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3151-1023G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158894727 | ||||||
| chr4:158895344
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3151-406T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158895344 | ||||||
| chr4:158895610
|
G | T | 2 | a0001c0001t0001g0040a0001c0001t0008g0092 | 2 | NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3151-140G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 15/16 | chr4 | 158895610 | ||||||
| chr4:158895973
|
C | T | 4 | a0001c0007t0006g0012a0001c0007t0006g0163a0001c0007t0006g0164others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3266+108C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158895973 | ||||||
| chr4:158896254
|
GGCACATT | G | 4 | a0003c0004t0001g0054a0003c0004t0001g0055a0003c0004t0001g0057others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+390_3266+396d others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896254 | ||||||
| chr4:158896497
|
TTTGGG | T | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3266+633_3266+637d others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896497 | ||||||
| chr4:158896503
|
G | A | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3266+638G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896503 | ||||||
| chr4:158896777
|
G | GT | 19 | a0001c0001t0001g0117a0001c0001t0005g0159a0001c0003t0004g0016others(16): Show | 19 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.3266+924dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896777 | |||||
| chr4:158896816
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3266+951C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896816 | ||||||
| chr4:158896841
|
G | GT | 43 | a0001c0001t0003g0184a0001c0007t0006g0163a0001c0007t0006g0164others(40): Show | 43 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.3266+986dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896841 | |||||
| chr4:158896841
|
G | GTT | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3266+985_3266+986d others(4): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158896841 | |||||
| chr4:158896851
|
T | A | 4 | a0001c0001t0007g0032a0002c0002t0007g0169a0002c0002t0007g0170others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+986T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158896851 | ||||||
| chr4:158897036
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0073others(5): Show | 8 | HG00438.hp1 HG01261.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.3266+1171C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897036 | ||||||
| chr4:158897154
|
C | T | 1 | a0005c0018t0003g0183 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3266+1289C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897154 | ||||||
| chr4:158897201
|
A | C | 1 | a0001c0009t0002g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3266+1336A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897201 | ||||||
| chr4:158897205
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3266+1340T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897205 | ||||||
| chr4:158897412
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0002c0017t0003g0030 | 3 | HG02258.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3266+1547G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897412 | ||||||
| chr4:158897531
|
G | A | 2 | a0002c0002t0003g0025a0002c0002t0003g0171 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3266+1666G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897531 | ||||||
| chr4:158897796
|
C | A | 1 | a0001c0001t0002g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3266+1931C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158897796 | ||||||
| chr4:158898031
|
G | A | 1 | a0002c0002t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3266+2166G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898031 | ||||||
| chr4:158898104
|
C | T | 35 | a0001c0001t0002g0001a0001c0001t0002g0203a0001c0001t0002g0204others(32): Show | 36 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.3266+2239C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898104 | ||||||
| chr4:158898176
|
A | T | 116 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.3266+2311A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898176 | ||||||
| chr4:158898237
|
G | A | 3 | a0002c0002t0003g0193a0002c0002t0003g0194a0002c0002t0003g0195 | 3 | NA18951.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3266+2372G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898237 | ||||||
| chr4:158898374
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(124): Show | 127 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.3266+2509G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898374 | ||||||
| chr4:158898600
|
A | G | 1 | a0001c0007t0006g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3266+2735A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898600 | ||||||
| chr4:158898645
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3266+2780T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898645 | ||||||
| chr4:158898658
|
C | T | 4 | a0001c0001t0007g0031a0001c0001t0007g0032a0002c0002t0007g0169others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+2793C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898658 | ||||||
| chr4:158898769
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3266+2904G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898769 | ||||||
| chr4:158898824
|
A | C | 2 | a0001c0001t0002g0208a0001c0001t0002g0226 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3266+2959A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898824 | ||||||
| chr4:158898998
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 4 | HG03491.hp2 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266+3133T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158898998 | ||||||
| chr4:158899109
|
C | G | 1 | a0001c0003t0004g0126 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3266+3244C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899109 | ||||||
| chr4:158899535
|
A | G | 1 | a0002c0002t0003g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3266+3670A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899535 | ||||||
| chr4:158899755
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3266+3890G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899755 | ||||||
| chr4:158899946
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3266+4081C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899946 | ||||||
| chr4:158899981
|
T | C | 1 | a0002c0002t0003g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3266+4116T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158899981 | ||||||
| chr4:158900006
|
A | T | 5 | a0001c0001t0002g0237a0001c0001t0002g0240a0001c0001t0002g0241others(2): Show | 5 | HG01934.hp1 NA18955.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.3266+4141A>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900006 | ||||||
| chr4:158900216
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3267-4250T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900216 | ||||||
| chr4:158900350
|
A | G | 1 | a0001c0014t0020g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3267-4116A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900350 | ||||||
| chr4:158900582
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3267-3884A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900582 | ||||||
| chr4:158900704
|
CTTTAT | C | 3 | a0002c0002t0003g0166a0002c0002t0003g0185a0002c0002t0003g0201 | 3 | HG00738.hp1 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.3267-3758_3267-375 others(9): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158900704 | |||||
| chr4:158900826
|
C | T | 2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3267-3640C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900826 | ||||||
| chr4:158900853
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3267-3613A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900853 | ||||||
| chr4:158900963
|
T | C | 7 | a0001c0003t0004g0018a0001c0003t0004g0019a0001c0003t0004g0020others(4): Show | 7 | HG02055.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3267-3503T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900963 | ||||||
| chr4:158900986
|
C | T | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.3267-3480C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158900986 | ||||||
| chr4:158901128
|
A | AT | 47 | a0001c0001t0001g0039a0001c0001t0001g0064a0001c0001t0001g0067others(44): Show | 47 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3267-3316dupT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | |||||
| chr4:158901128
|
A | ATT | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0041others(83): Show | 87 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.3267-3317_3267-331 others(6): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | |||||
| chr4:158901128
|
A | ATTT | 14 | a0001c0001t0002g0237a0001c0001t0002g0238a0001c0001t0002g0240others(11): Show | 14 | HG00597.hp2 HG01884.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.3267-3318_3267-331 others(7): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | |||||
| chr4:158901128
|
AT | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0063others(4): Show | 7 | HG00597.hp1 HG00639.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3267-3316delT | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | |||||
| chr4:158901128
|
ATTTTTTT others(4): Show |
A | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3267-3326_3267-331 others(15): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158901128 | |||||
| chr4:158901194
|
G | A | 1 | a0003c0004t0001g0150 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3267-3272G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901194 | ||||||
| chr4:158901238
|
A | G | 1 | a0002c0002t0003g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3267-3228A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901238 | ||||||
| chr4:158901287
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3267-3179G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901287 | ||||||
| chr4:158901502
|
T | G | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0221others(1): Show | 4 | HG00639.hp2 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2964T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901502 | ||||||
| chr4:158901634
|
G | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3267-2832G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901634 | ||||||
| chr4:158901717
|
C | T | 1 | a0001c0001t0009g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3267-2749C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901717 | ||||||
| chr4:158901744
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(1): Show | 4 | HG03491.hp2 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2722A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901744 | ||||||
| chr4:158901901
|
G | T | 16 | a0001c0003t0004g0016a0001c0003t0004g0018a0001c0003t0004g0019others(13): Show | 16 | HG00609.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.3267-2565G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901901 | ||||||
| chr4:158901911
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG01517.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3267-2555T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158901911 | ||||||
| chr4:158902130
|
A | G | 1 | a0011c0013t0008g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3267-2336A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902130 | ||||||
| chr4:158902145
|
C | T | 1 | a0003c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3267-2321C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902145 | ||||||
| chr4:158902278
|
A | G | 4 | a0002c0002t0003g0190a0002c0002t0003g0191a0002c0002t0003g0196others(1): Show | 4 | NA18966.hp1 NA18967.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-2188A>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902278 | ||||||
| chr4:158902296
|
C | G | 3 | a0001c0007t0006g0163a0001c0007t0006g0164a0001c0007t0006g0165 | 3 | HG02055.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3267-2170C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902296 | ||||||
| chr4:158902419
|
C | T | 50 | a0001c0001t0002g0001a0001c0001t0002g0202a0001c0001t0002g0203others(47): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.3267-2047C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902419 | ||||||
| chr4:158902521
|
G | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0040others(75): Show | 78 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3267-1945G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902521 | ||||||
| chr4:158902625
|
G | A | 4 | a0001c0003t0004g0024a0001c0003t0004g0125a0001c0003t0004g0126others(1): Show | 4 | HG00609.hp2 HG02135.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.3267-1841G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902625 | ||||||
| chr4:158902719
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3267-1747G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902719 | ||||||
| chr4:158902955
|
C | CGGCTCCC others(5): Show |
2 | a0001c0008t0010g0033a0001c0008t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3267-1502_3267-150 others(16): Show |
FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr4 | 158902955 | |||||
| chr4:158902955
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3267-1511C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158902955 | ||||||
| chr4:158903103
|
G | A | 1 | a0002c0002t0003g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3267-1363G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903103 | ||||||
| chr4:158903383
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3267-1083G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903383 | ||||||
| chr4:158903426
|
G | A | 1 | a0008c0012t0002g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3267-1040G>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903426 | ||||||
| chr4:158903541
|
C | G | 2 | a0001c0001t0003g0036a0002c0002t0003g0172 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3267-925C>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903541 | ||||||
| chr4:158903619
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3267-847C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903619 | ||||||
| chr4:158903843
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3267-623C>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903843 | ||||||
| chr4:158903909
|
T | G | 1 | a0001c0001t0009g0231 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3267-557T>G | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158903909 | ||||||
| chr4:158904039
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(249): Show | 253 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.3267-427T>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904039 | ||||||
| chr4:158904105
|
A | C | 1 | a0001c0001t0005g0011 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3267-361A>C | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904105 | ||||||
| chr4:158904127
|
T | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(248): Show | 252 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.3267-339T>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904127 | ||||||
| chr4:158904148
|
G | T | 10 | a0003c0004t0001g0053a0003c0004t0001g0054a0003c0004t0001g0055others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.3267-318G>T | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904148 | ||||||
| chr4:158904242
|
C | A | 34 | a0001c0001t0003g0184a0002c0002t0003g0025a0002c0002t0003g0104others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.3267-224C>A | FNIP2 | ENSG00000052795.13 | transcript | ENST00000264433.11 | protein_coding | 16/16 | chr4 | 158904242 |