Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9855 |
|---|---|
| ensemblid | ENSG00000006607.14 |
| hgncid | 16460 |
| symbol | FARP2 |
| name | FERM, ARH/RhoGEF and pleckstrin domain protein 2 |
| refseq_nuc | NM_014808.4 |
| refseq_prot | NP_055623.1 |
| ensembl_nuc | ENST00000264042.8 |
| ensembl_prot | ENSP00000264042.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 241356285 |
| end | 241494841 |
| strand | + |
| ver | v1.2 |
| region | chr2:241356285-241494841 |
| region5000 | chr2:241351285-241499841 |
| regionname0 | FARP2_chr2_241356285_241494841 |
| regionname5000 | FARP2_chr2_241351285_241499841 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1054 | 273 | 49 | 44 | 135 | 8 | 35 | 98 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0002 | 0/0 | 1054 | 34 | 0 | 13 | 21 | 0 | 0 | 18 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0003 | 0/0 | 1054 | 28 | 10 | 5 | 6 | 1 | 6 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0004 | 0/0 | 1054 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0005 | 0/0 | 1054 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0006 | 0/0 | 1054 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0007 | 0/0 | 1054 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0008 | 0/0 | 1054 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0009 | 0/0 | 1054 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0010 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0011 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0012 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0013 | 0/0 | 1054 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0014 | 0/0 | 1054 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0015 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0016 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0017 | 0/0 | 1054 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0018 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0019 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0020 | 0/0 | 1054 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3165 | 186 | 28 | 24 | 104 | 4 | 25 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0002 | 0/0 | 3165 | 34 | 0 | 13 | 21 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0003 | 0/0 | 3165 | 34 | 3 | 5 | 21 | 1 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0004 | 0/0 | 3165 | 30 | 14 | 11 | 0 | 3 | 2 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0005 | 0/0 | 3165 | 28 | 10 | 5 | 6 | 1 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0006 | 0/0 | 3165 | 13 | 0 | 1 | 8 | 0 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0007 | 0/0 | 3165 | 11 | 9 | 2 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0008 | 0/0 | 3165 | 8 | 8 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0009 | 0/0 | 3165 | 5 | 0 | 5 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0010 | 0/0 | 3165 | 3 | 0 | 3 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0011 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0012 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0013 | 0/0 | 3165 | 2 | 1 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0014 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0015 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0016 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0017 | 0/0 | 3165 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0018 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0019 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0020 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0021 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0022 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0023 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0024 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0025 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0026 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0027 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0028 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0029 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0030 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0031 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| c0032 | 0/1 | 3165 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 845 | 365 | 80 | 66 | 162 | 11 | 44 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0002 | 0/0 | 845 | 5 | 4 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0003 | 0/0 | 845 | 2 | 0 | 1 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0004 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0005 | 0/0 | 845 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0006 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0007 | 0/0 | 845 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0008 | 0/0 | 845 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| t0009 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3165 | 186 | 28 | 24 | 104 | 4 | 25 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0003 | 0/0 | 3165 | 34 | 3 | 5 | 21 | 1 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0004 | 0/0 | 3165 | 30 | 14 | 11 | 0 | 3 | 2 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0006 | 0/0 | 3165 | 13 | 0 | 1 | 8 | 0 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0010 | 0/0 | 3165 | 3 | 0 | 3 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0011 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0015 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0019 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0022 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0025 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0032 | 0/1 | 3165 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0002c0002 | 0/0 | 3165 | 34 | 0 | 13 | 21 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0003c0005 | 0/0 | 3165 | 28 | 10 | 5 | 6 | 1 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0004c0007 | 0/0 | 3165 | 11 | 9 | 2 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0005c0008 | 0/0 | 3165 | 8 | 8 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0005c0014 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0006c0009 | 0/0 | 3165 | 5 | 0 | 5 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0007c0013 | 0/0 | 3165 | 2 | 1 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0008c0021 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0008c0028 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0009c0012 | 0/0 | 3165 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0010c0026 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0011c0020 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0012c0023 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0013c0024 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0014c0018 | 0/0 | 3165 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0015c0029 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0016c0030 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0017c0017 | 0/0 | 3165 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0018c0016 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0019c0027 | 0/0 | 3165 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0020c0031 | 0/0 | 3165 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4009 | 179 | 23 | 22 | 104 | 4 | 25 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0001t0002 | 0/0 | 4009 | 4 | 3 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0001t0004 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0001t0005 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0001t0009 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0003t0001 | 0/0 | 4009 | 32 | 3 | 4 | 20 | 1 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0003t0007 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0003t0008 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0004t0001 | 0/0 | 4009 | 30 | 14 | 11 | 0 | 3 | 2 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0006t0001 | 0/0 | 4009 | 13 | 0 | 1 | 8 | 0 | 4 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0010t0001 | 0/0 | 4009 | 3 | 0 | 3 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0011t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0015t0002 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0019t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0022t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0025t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0001c0032t0001 | 0/1 | 4009 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0002c0002t0001 | 0/0 | 4009 | 33 | 0 | 13 | 20 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0002c0002t0006 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0003c0005t0001 | 0/0 | 4009 | 27 | 10 | 4 | 6 | 1 | 6 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0003c0005t0003 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0004c0007t0001 | 0/0 | 4009 | 11 | 9 | 2 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0005c0008t0001 | 0/0 | 4009 | 8 | 8 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0005c0014t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0006c0009t0001 | 0/0 | 4009 | 5 | 0 | 5 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0007c0013t0001 | 0/0 | 4009 | 2 | 1 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0008c0021t0003 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0008c0028t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0009c0012t0001 | 0/0 | 4009 | 2 | 2 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0010c0026t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0011c0020t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0012c0023t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0013c0024t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0014c0018t0001 | 0/0 | 4009 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0015c0029t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0016c0030t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0017c0017t0001 | 0/0 | 4009 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0018c0016t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0019c0027t0001 | 0/0 | 4009 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| a0020c0031t0001 | 0/0 | 4009 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | copy fasta | chr2 | 241351285 | 241499841 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0002g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0003t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0004t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0010t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0010t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0010t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0011t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0011t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0015t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0019t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0022t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0025t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0001c0032t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0002c0002t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0003c0005t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0004c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0008t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0014t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0005c0014t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0006c0009t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0006c0009t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0006c0009t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0006c0009t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0006c0009t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0007c0013t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0007c0013t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0008c0021t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0008c0028t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0009c0012t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0009c0012t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0010c0026t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0011c0020t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0012c0023t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0013c0024t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0014c0018t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0015c0029t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0016c0030t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0017c0017t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0018c0016t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0019c0027t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| a0020c0031t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0005 | t0001 | g0040 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0170 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0172 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00140 | hp2 | a0008 | c0021 | t0003 | g0334 | EUR | GBR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0033 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00323 | hp1 | a0011 | c0020 | t0001 | g0155 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00408 | hp1 | a0001 | c0006 | t0001 | g0244 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00597 | hp2 | a0001 | c0006 | t0001 | g0245 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00621 | hp2 | a0001 | c0006 | t0001 | g0242 | EAS | CHS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0173 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0347 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0349 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG00741 | hp2 | a0001 | c0010 | t0001 | g0365 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0169 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01069 | hp2 | a0001 | c0010 | t0001 | g0364 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0178 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0180 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01071 | hp2 | a0001 | c0010 | t0001 | g0363 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0174 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0344 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01081 | hp2 | a0006 | c0009 | t0001 | g0187 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01099 | hp1 | a0004 | c0007 | t0001 | g0106 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01106 | hp1 | a0001 | c0003 | t0008 | g0061 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01109 | hp1 | a0004 | c0007 | t0001 | g0129 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0165 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01168 | hp2 | a0006 | c0009 | t0001 | g0183 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01169 | hp1 | a0006 | c0009 | t0001 | g0184 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0181 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0357 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01192 | hp2 | a0001 | c0006 | t0001 | g0243 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0177 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0350 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0171 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01261 | hp1 | a0006 | c0009 | t0001 | g0185 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0372 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0182 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0348 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0179 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0120 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01496 | hp2 | a0003 | c0005 | t0001 | g0190 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0199 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01928 | hp1 | a0003 | c0005 | t0001 | g0008 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01934 | hp2 | a0003 | c0005 | t0001 | g0194 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0345 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01981 | hp1 | a0017 | c0017 | t0001 | g0255 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0352 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0351 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02004 | hp2 | a0003 | c0005 | t0003 | g0058 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02055 | hp1 | a0008 | c0028 | t0001 | g0018 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02055 | hp2 | a0003 | c0005 | t0001 | g0046 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02056 | hp1 | a0001 | c0006 | t0001 | g0241 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02071 | hp2 | a0001 | c0006 | t0001 | g0240 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02145 | hp2 | a0007 | c0013 | t0001 | g0191 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02155 | hp1 | a0001 | c0022 | t0001 | g0124 | EAS | CDX | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CDX | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0359 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0378 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02258 | hp2 | a0004 | c0007 | t0001 | g0156 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02451 | hp1 | a0003 | c0005 | t0001 | g0196 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02451 | hp2 | a0005 | c0008 | t0001 | g0147 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0164 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0375 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02615 | hp1 | a0005 | c0008 | t0001 | g0153 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02622 | hp1 | a0003 | c0005 | t0001 | g0198 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02630 | hp1 | a0005 | c0008 | t0001 | g0152 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02630 | hp2 | a0009 | c0012 | t0001 | g0002 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02647 | hp1 | a0005 | c0008 | t0001 | g0154 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0021 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02698 | hp2 | a0001 | c0006 | t0001 | g0246 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02717 | hp1 | a0004 | c0007 | t0001 | g0096 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02735 | hp1 | a0020 | c0031 | t0001 | g0019 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0373 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02818 | hp1 | a0001 | c0011 | t0001 | g0107 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02818 | hp2 | a0009 | c0012 | t0001 | g0001 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02886 | hp1 | a0001 | c0011 | t0001 | g0108 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02886 | hp2 | a0004 | c0007 | t0001 | g0114 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02895 | hp2 | a0004 | c0007 | t0001 | g0101 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0175 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02897 | hp2 | a0004 | c0007 | t0001 | g0102 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02965 | hp1 | a0015 | c0029 | t0001 | g0029 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02965 | hp2 | a0012 | c0023 | t0001 | g0203 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02970 | hp2 | a0005 | c0008 | t0001 | g0148 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0370 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0167 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03098 | hp2 | a0004 | c0007 | t0001 | g0097 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0193 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0104 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03139 | hp1 | a0005 | c0008 | t0001 | g0146 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03139 | hp2 | a0001 | c0025 | t0001 | g0160 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03195 | hp1 | a0004 | c0007 | t0001 | g0128 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03195 | hp2 | a0003 | c0005 | t0001 | g0197 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0159 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03239 | hp2 | a0003 | c0005 | t0001 | g0050 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03486 | hp1 | a0005 | c0014 | t0001 | g0149 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03486 | hp2 | a0004 | c0007 | t0001 | g0100 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03490 | hp1 | a0003 | c0005 | t0001 | g0042 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0010 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03492 | hp1 | a0003 | c0005 | t0001 | g0041 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03516 | hp1 | a0003 | c0005 | t0001 | g0369 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0362 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03540 | hp2 | a0019 | c0027 | t0001 | g0145 | AFR | GWD | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03579 | hp1 | a0005 | c0008 | t0001 | g0144 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03688 | hp2 | a0003 | c0005 | t0001 | g0059 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03831 | hp2 | a0001 | c0006 | t0001 | g0251 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03834 | hp1 | a0003 | c0005 | t0001 | g0052 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03927 | hp1 | a0010 | c0026 | t0001 | g0116 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0249 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04184 | hp2 | a0003 | c0005 | t0001 | g0039 | SAS | BEB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0176 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0250 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18522 | hp2 | a0003 | c0005 | t0001 | g0195 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0360 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18906 | hp2 | a0001 | c0015 | t0002 | g0371 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18945 | hp2 | a0001 | c0019 | t0001 | g0111 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18951 | hp2 | a0002 | c0002 | t0006 | g0252 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18953 | hp2 | a0003 | c0005 | t0001 | g0045 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18963 | hp2 | a0003 | c0005 | t0001 | g0044 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18964 | hp2 | a0003 | c0005 | t0001 | g0051 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18970 | hp2 | a0014 | c0018 | t0001 | g0339 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18972 | hp1 | a0001 | c0003 | t0007 | g0036 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18984 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18988 | hp1 | a0013 | c0024 | t0001 | g0087 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18998 | hp2 | a0003 | c0005 | t0001 | g0048 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19002 | hp2 | a0003 | c0005 | t0001 | g0043 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0361 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19043 | hp2 | a0004 | c0007 | t0001 | g0127 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19074 | hp1 | a0003 | c0005 | t0001 | g0047 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19077 | hp1 | a0001 | c0006 | t0001 | g0248 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19085 | hp2 | a0001 | c0006 | t0001 | g0247 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19240 | hp1 | a0003 | c0005 | t0001 | g0192 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | YRI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ASW | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0166 | EUR | TSI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20805 | hp2 | a0018 | c0016 | t0001 | g0321 | EUR | TSI | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20905 | hp1 | a0007 | c0013 | t0001 | g0028 | SAS | GIH | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01123 | hp1 | a0003 | c0005 | t0001 | g0057 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG01123 | hp2 | a0006 | c0009 | t0001 | g0186 | AMR | CLM | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02486 | hp1 | a0016 | c0030 | t0001 | g0006 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0374 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0162 | AFR | MSL | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG06807 | hp1 | a0005 | c0008 | t0001 | g0150 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20300 | hp1 | a0005 | c0014 | t0001 | g0151 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| NA21309 | hp2 | a0003 | c0005 | t0001 | g0049 | AFR | LWK | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0032 | t0001 | g0227 | REF | REF | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | FARP2_chr2_241351285_241499841 | FARP2 | chr2 | 241351285 | 241499841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241373157
|
G | A | 1 | a0006 | 5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
missense_variant | MODERATE | c.50G>A | p.Arg17His | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/27 | 178/4009 | 50/3165 | 17/1054 | chr2 | 241373157 | ||
| chr2:241373241
|
A | G | 1 | a0020 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.134A>G | p.His45Arg | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/27 | 262/4009 | 134/3165 | 45/1054 | chr2 | 241373241 | ||
| chr2:241413353
|
A | C | 2 | a0005a0019 | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
missense_variant | MODERATE | c.555A>C | p.Lys185Asn | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/27 | 683/4009 | 555/3165 | 185/1054 | chr2 | 241413353 | ||
| chr2:241431686
|
C | T | 2 | a0003a0007 | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
missense_variant | MODERATE | c.779C>T | p.Thr260Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/27 | 907/4009 | 779/3165 | 260/1054 | chr2 | 241431686 | ||
| chr2:241441319
|
G | A | 1 | a0018 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1174G>A | p.Glu392Lys | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1302/4009 | 1174/3165 | 392/1054 | chr2 | 241441319 | ||
| chr2:241456756
|
C | T | 1 | a0010 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1421C>T | p.Thr474Met | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/27 | 1549/4009 | 1421/3165 | 474/1054 | chr2 | 241456756 | ||
| chr2:241462601
|
G | A | 1 | a0011 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1666G>A | p.Val556Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/27 | 1794/4009 | 1666/3165 | 556/1054 | chr2 | 241462601 | ||
| chr2:241468173
|
G | A | 3 | a0003a0008a0019 | 31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
missense_variant | MODERATE | c.1927G>A | p.Val643Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2055/4009 | 1927/3165 | 643/1054 | chr2 | 241468173 | ||
| chr2:241468312
|
G | A | 1 | a0012 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2066G>A | p.Arg689His | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2194/4009 | 2066/3165 | 689/1054 | chr2 | 241468312 | ||
| chr2:241468326
|
C | T | 1 | a0013 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.2080C>T | p.Arg694Cys | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2208/4009 | 2080/3165 | 694/1054 | chr2 | 241468326 | ||
| chr2:241475910
|
C | T | 1 | a0004 | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
missense_variant | MODERATE | c.2185C>T | p.Arg729Trp | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/27 | 2313/4009 | 2185/3165 | 729/1054 | chr2 | 241475910 | ||
| chr2:241475962
|
T | C | 1 | a0017 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.2237T>C | p.Ile746Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/27 | 2365/4009 | 2237/3165 | 746/1054 | chr2 | 241475962 | ||
| chr2:241490013
|
G | A | 1 | a0012 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2473G>A | p.Ala825Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/27 | 2601/4009 | 2473/3165 | 825/1054 | chr2 | 241490013 | ||
| chr2:241491065
|
C | T | 1 | a0016 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2509C>T | p.Arg837Trp | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/27 | 2637/4009 | 2509/3165 | 837/1054 | chr2 | 241491065 | ||
| chr2:241491173
|
C | T | 1 | a0009 | 2 | HG02630.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.2617C>T | p.Pro873Ser | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/27 | 2745/4009 | 2617/3165 | 873/1054 | chr2 | 241491173 | ||
| chr2:241491579
|
C | T | 3 | a0002a0014a0017 | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
missense_variant | MODERATE | c.2687C>T | p.Ser896Phe | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/27 | 2815/4009 | 2687/3165 | 896/1054 | chr2 | 241491579 | ||
| chr2:241491618
|
T | C | 1 | a0014 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2726T>C | p.Met909Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/27 | 2854/4009 | 2726/3165 | 909/1054 | chr2 | 241491618 | ||
| chr2:241493404
|
G | A | 1 | a0015 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3007G>A | p.Val1003Ile | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/27 | 3135/4009 | 3007/3165 | 1003/1054 | chr2 | 241493404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241373128
|
A | C | 1 | a0001c0032 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.21A>C | p.Thr7Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/27 | 149/4009 | 21/3165 | 7/1054 | chr2 | 241373128 | ||
| chr2:241411051
|
A | G | 5 | a0001c0003a0008c0028a0015c0029others(2): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
synonymous_variant | LOW | c.429A>G | p.Gln143Gln | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/27 | 557/4009 | 429/3165 | 143/1054 | chr2 | 241411051 | ||
| chr2:241413332
|
G | A | 1 | a0001c0011 | 2 | HG02818.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.534G>A | p.Thr178Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/27 | 662/4009 | 534/3165 | 178/1054 | chr2 | 241413332 | ||
| chr2:241436502
|
G | A | 1 | a0001c0015 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1122G>A | p.Thr374Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/27 | 1250/4009 | 1122/3165 | 374/1054 | chr2 | 241436502 | ||
| chr2:241441333
|
T | A | 4 | a0001c0006a0002c0002a0014c0018others(1): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
synonymous_variant | LOW | c.1188T>A | p.Thr396Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1316/4009 | 1188/3165 | 396/1054 | chr2 | 241441333 | ||
| chr2:241441516
|
G | A | 1 | a0001c0019 | 1 | NA18945.hp2 | synonymous_variant | LOW | c.1371G>A | p.Ser457Ser | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/27 | 1499/4009 | 1371/3165 | 457/1054 | chr2 | 241441516 | ||
| chr2:241462609
|
C | T | 2 | a0001c0025a0005c0008 | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
synonymous_variant | LOW | c.1674C>T | p.Thr558Thr | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/27 | 1802/4009 | 1674/3165 | 558/1054 | chr2 | 241462609 | ||
| chr2:241463391
|
G | C | 1 | a0001c0010 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.1734G>C | p.Leu578Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/27 | 1862/4009 | 1734/3165 | 578/1054 | chr2 | 241463391 | ||
| chr2:241468244
|
G | A | 1 | a0001c0022 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1998G>A | p.Leu666Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2126/4009 | 1998/3165 | 666/1054 | chr2 | 241468244 | ||
| chr2:241468331
|
A | G | 2 | a0001c0004a0001c0010 | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.2085A>G | p.Leu695Leu | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/27 | 2213/4009 | 2085/3165 | 695/1054 | chr2 | 241468331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241356286
|
G | C | 1 | a0001c0001t0004 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/27 | 16822 | chr2 | 241356286 | |||||
| chr2:241356355
|
G | A | 2 | a0001c0001t0002a0001c0015t0002 | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-58G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/27 | 16753 | chr2 | 241356355 | |||||
| chr2:241494371
|
G | A | 1 | a0001c0001t0005 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 246 | chr2 | 241494371 | |||||
| chr2:241494492
|
G | A | 1 | a0002c0002t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 367 | chr2 | 241494492 | |||||
| chr2:241494538
|
C | T | 2 | a0003c0005t0003a0008c0021t0003 | 2 | HG00140.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*413C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 413 | chr2 | 241494538 | |||||
| chr2:241494575
|
G | A | 1 | a0001c0003t0007 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 450 | chr2 | 241494575 | |||||
| chr2:241494613
|
G | A | 1 | a0001c0003t0008 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 488 | chr2 | 241494613 | |||||
| chr2:241494660
|
G | T | 1 | a0001c0001t0009 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 27/27 | 535 | chr2 | 241494660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241356420
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+32G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356420 | ||||||
| chr2:241356514
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-25+126T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356514 | ||||||
| chr2:241356799
|
A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+411A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356799 | ||||||
| chr2:241356816
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-25+428C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356816 | ||||||
| chr2:241356845
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+457G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356845 | ||||||
| chr2:241356858
|
G | C | 57 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.-25+470G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356858 | ||||||
| chr2:241356863
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-25+475G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241356863 | ||||||
| chr2:241357015
|
C | G | 2 | a0001c0001t0001g0376a0001c0001t0001g0377 | 2 | NA18968.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-25+627C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357015 | ||||||
| chr2:241357034
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(189): Show | 192 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.-25+646A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357034 | ||||||
| chr2:241357154
|
A | T | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-25+766A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357154 | ||||||
| chr2:241357221
|
C | A | 10 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+833C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357221 | ||||||
| chr2:241357313
|
G | A | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-25+925G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357313 | ||||||
| chr2:241357341
|
ACAG | A | 9 | a0001c0001t0001g0378a0001c0001t0002g0372a0001c0001t0002g0373others(6): Show | 9 | HG01261.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+954_-25+956del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357341 | ||||||
| chr2:241357402
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG00558.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-25+1014C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357402 | ||||||
| chr2:241357425
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-25+1037G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357425 | ||||||
| chr2:241357676
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-25+1288C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357676 | ||||||
| chr2:241357703
|
G | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(178): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-25+1315G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357703 | ||||||
| chr2:241357757
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+1369C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357757 | ||||||
| chr2:241357776
|
C | T | 2 | a0003c0005t0001g0198a0003c0005t0001g0199 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-25+1388C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357776 | ||||||
| chr2:241357843
|
A | G | 1 | a0004c0007t0001g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-25+1455A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357843 | ||||||
| chr2:241357925
|
A | G | 2 | a0001c0003t0001g0060a0001c0003t0008g0061 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-25+1537A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357925 | ||||||
| chr2:241357984
|
G | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-25+1596G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241357984 | ||||||
| chr2:241358186
|
C | T | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-25+1798C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358186 | ||||||
| chr2:241358203
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1815A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358203 | ||||||
| chr2:241358209
|
A | T | 2 | a0003c0005t0001g0057a0003c0005t0003g0058 | 2 | HG01123.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-25+1821A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358209 | ||||||
| chr2:241358426
|
A | G | 5 | a0006c0009t0001g0183a0006c0009t0001g0184a0006c0009t0001g0185others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+2038A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358426 | ||||||
| chr2:241358648
|
G | A | 1 | a0002c0002t0001g0200 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-25+2260G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358648 | ||||||
| chr2:241358696
|
C | T | 6 | a0001c0004t0001g0177a0001c0004t0001g0178a0001c0004t0001g0179others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2308C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358696 | ||||||
| chr2:241358748
|
G | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+2360G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358748 | ||||||
| chr2:241358813
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+2425G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358813 | ||||||
| chr2:241358866
|
C | T | 26 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-25+2478C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358866 | ||||||
| chr2:241358920
|
T | C | 3 | a0001c0001t0001g0378a0009c0012t0001g0001a0009c0012t0001g0002 | 3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+2532T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241358920 | ||||||
| chr2:241359078
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-25+2690T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359078 | ||||||
| chr2:241359293
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-25+2905A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359293 | ||||||
| chr2:241359338
|
C | G | 1 | a0006c0009t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+2950C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359338 | ||||||
| chr2:241359421
|
T | C | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-25+3033T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359421 | ||||||
| chr2:241359453
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0378 | 3 | HG02257.hp1 HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+3065G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359453 | ||||||
| chr2:241359517
|
C | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-25+3129C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359517 | ||||||
| chr2:241359786
|
T | G | 1 | a0003c0005t0001g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-25+3398T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241359786 | ||||||
| chr2:241360141
|
A | G | 3 | a0001c0010t0001g0363a0001c0010t0001g0364a0001c0010t0001g0365 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-25+3753A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360141 | ||||||
| chr2:241360164
|
G | T | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-25+3776G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360164 | ||||||
| chr2:241360254
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-25+3866G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360254 | ||||||
| chr2:241360368
|
C | T | 8 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+3980C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360368 | ||||||
| chr2:241360660
|
C | G | 4 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+4272C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360660 | ||||||
| chr2:241360661
|
G | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+4273G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360661 | ||||||
| chr2:241360668
|
T | C | 4 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+4280T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360668 | ||||||
| chr2:241360673
|
C | CA | 137 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(134): Show | 137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-25+4302dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241360673 | |||||
| chr2:241360673
|
C | CAA | 11 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0366others(8): Show | 11 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+4301_-25+4302d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241360673 | |||||
| chr2:241360804
|
C | A | 11 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(8): Show | 11 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+4416C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241360804 | ||||||
| chr2:241361028
|
G | GA | 34 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-25+4654dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241361028 | |||||
| chr2:241361028
|
GA | G | 36 | a0001c0001t0001g0142a0001c0001t0001g0158a0001c0004t0001g0143others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-25+4654delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241361028 | |||||
| chr2:241361041
|
A | AC | 25 | a0002c0002t0001g0200a0002c0002t0001g0335a0002c0002t0001g0336others(22): Show | 25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25+4653_-25+4654i others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361041 | ||||||
| chr2:241361041
|
A | C | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+4653A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361041 | ||||||
| chr2:241361044
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-25+4656A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361044 | ||||||
| chr2:241361075
|
A | G | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-25+4687A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361075 | ||||||
| chr2:241361091
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4703T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361091 | ||||||
| chr2:241361092
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4704G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361092 | ||||||
| chr2:241361093
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+4705G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361093 | ||||||
| chr2:241361135
|
A | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+4747A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361135 | ||||||
| chr2:241361191
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-25+4803C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361191 | ||||||
| chr2:241361236
|
A | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-25+4848A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361236 | ||||||
| chr2:241361622
|
C | T | 1 | a0008c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+5234C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361622 | ||||||
| chr2:241361675
|
T | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+5287T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361675 | ||||||
| chr2:241361682
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-25+5294A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361682 | ||||||
| chr2:241361948
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-25+5560G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361948 | ||||||
| chr2:241361998
|
G | A | 2 | a0006c0009t0001g0183a0006c0009t0001g0184 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-25+5610G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241361998 | ||||||
| chr2:241362429
|
C | T | 10 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+6041C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362429 | ||||||
| chr2:241362471
|
G | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-25+6083G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362471 | ||||||
| chr2:241362494
|
C | T | 1 | a0001c0004t0001g0176 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-25+6106C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362494 | ||||||
| chr2:241362552
|
A | G | 25 | a0002c0002t0001g0200a0002c0002t0001g0335a0002c0002t0001g0336others(22): Show | 25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25+6164A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362552 | ||||||
| chr2:241362567
|
T | C | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+6179T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362567 | ||||||
| chr2:241362767
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-25+6379G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241362767 | ||||||
| chr2:241363118
|
C | T | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+6730C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363118 | ||||||
| chr2:241363396
|
A | G | 97 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(94): Show | 97 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-25+7008A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363396 | ||||||
| chr2:241363414
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-25+7026C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363414 | ||||||
| chr2:241363416
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-25+7028G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363416 | ||||||
| chr2:241363430
|
G | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+7042G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363430 | ||||||
| chr2:241363444
|
G | A | 4 | a0001c0006t0001g0240a0001c0006t0001g0241a0001c0006t0001g0242others(1): Show | 4 | HG00621.hp2 HG01192.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+7056G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363444 | ||||||
| chr2:241363519
|
T | C | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+7131T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363519 | ||||||
| chr2:241363679
|
C | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-25+7291C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363679 | ||||||
| chr2:241363943
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-25+7555G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241363943 | ||||||
| chr2:241364041
|
T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-25+7653T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364041 | ||||||
| chr2:241364076
|
C | T | 3 | a0001c0001t0001g0378a0009c0012t0001g0001a0009c0012t0001g0002 | 3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-25+7688C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364076 | ||||||
| chr2:241364302
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25+7914G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364302 | ||||||
| chr2:241364558
|
A | C | 3 | a0001c0001t0001g0235a0001c0001t0001g0330a0001c0001t0001g0331 | 3 | NA18943.hp2 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-25+8170A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364558 | ||||||
| chr2:241364792
|
G | A | 16 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(13): Show | 16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24-8292G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364792 | ||||||
| chr2:241364927
|
C | G | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24-8157C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364927 | ||||||
| chr2:241364940
|
G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-8144G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241364940 | ||||||
| chr2:241365282
|
C | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-24-7802C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365282 | ||||||
| chr2:241365376
|
G | A | 48 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-7708G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365376 | ||||||
| chr2:241365695
|
G | A | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-7389G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365695 | ||||||
| chr2:241365697
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-24-7387A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365697 | ||||||
| chr2:241365742
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24-7342T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365742 | ||||||
| chr2:241365765
|
A | G | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-24-7319A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365765 | ||||||
| chr2:241365790
|
C | A | 48 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-7294C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241365790 | ||||||
| chr2:241365974
|
C | CT | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-7097dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241365974 | |||||
| chr2:241366092
|
TA | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(24): Show | 27 | HG00544.hp2 HG00639.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-24-6979delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366092 | |||||
| chr2:241366100
|
A | AATAT | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-24-6983_-24-6982i others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366100 | |||||
| chr2:241366100
|
A | T | 24 | a0003c0005t0001g0039a0003c0005t0001g0040a0003c0005t0001g0041others(21): Show | 24 | HG00099.hp1 HG02055.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-6984A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366100 | ||||||
| chr2:241366102
|
A | AAT | 8 | a0003c0005t0001g0190a0003c0005t0001g0195a0003c0005t0001g0196others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24-6981_-24-6980i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366102 | |||||
| chr2:241366102
|
A | AATATATA others(21): Show |
1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-24-6981_-24-6980i others(30): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366102 | |||||
| chr2:241366102
|
A | T | 117 | a0001c0003t0001g0007a0001c0003t0001g0011a0001c0003t0001g0012others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.-24-6982A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366102 | ||||||
| chr2:241366104
|
A | AAATATAT others(2): Show |
11 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 11 | HG01934.hp1 HG02071.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-6979_-24-6978i others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366104 | |||||
| chr2:241366104
|
A | AAATATAT others(4): Show |
15 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24-6979_-24-6978i others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366104 | |||||
| chr2:241366104
|
A | C | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-24-6980A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366104 | ||||||
| chr2:241366104
|
A | T | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0135others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-24-6980A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366104 | ||||||
| chr2:241366106
|
T | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0141a0004c0007t0001g0096others(1): Show | 4 | HG01099.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6978T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366106 | ||||||
| chr2:241366106
|
T | TATATATA others(19): Show |
24 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(21): Show | 24 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366106 | |||||
| chr2:241366108
|
T | TATATATA others(17): Show |
2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366108 | |||||
| chr2:241366108
|
T | TATATATA others(45): Show |
1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-24-6965_-24-6964i others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366108 | |||||
| chr2:241366109
|
A | ATATATAT others(5): Show |
1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-24-6967_-24-6966i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366109 | |||||
| chr2:241366110
|
T | TATATATA others(3): Show |
65 | a0001c0001t0001g0004a0001c0001t0001g0231a0001c0001t0001g0232others(62): Show | 65 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-6965_-24-6964i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366110 | |||||
| chr2:241366111
|
A | ATATATAT others(53): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0188a0004c0007t0001g0100others(2): Show | 5 | HG00558.hp1 HG02145.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | |||||
| chr2:241366111
|
A | ATATATAT others(55): Show |
39 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0093others(36): Show | 39 | HG00544.hp1 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | |||||
| chr2:241366111
|
A | ATATATAT others(53): Show |
1 | a0011c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-24-6963_-24-6962i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | |||||
| chr2:241366111
|
A | ATATATAT others(57): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(66): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | |||||
| chr2:241366111
|
A | ATATATAT others(57): Show |
5 | a0001c0001t0001g0095a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG01099.hp2 HG02083.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-6963_-24-6962i others(66): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366111 | |||||
| chr2:241366120
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6964T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366120 | ||||||
| chr2:241366122
|
C | T | 85 | a0001c0001t0001g0088a0001c0001t0001g0136a0001c0001t0001g0158others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.-24-6962C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366122 | ||||||
| chr2:241366123
|
G | A | 152 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0136others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.-24-6961G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366123 | ||||||
| chr2:241366123
|
GTA | G | 27 | a0001c0001t0001g0228a0001c0001t0001g0304a0001c0001t0001g0305others(24): Show | 27 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-24-6946_-24-6945d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366123 | |||||
| chr2:241366124
|
T | TATATATA others(5): Show |
1 | a0001c0006t0001g0246 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366124 | |||||
| chr2:241366125
|
A | ACACGTAT others(25): Show |
1 | a0001c0003t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24-6959_-24-6958i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366125 | ||||||
| chr2:241366125
|
A | ATACACGT others(27): Show |
1 | a0006c0009t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-24-6957_-24-6956i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATACGTAT others(25): Show |
33 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(30): Show | 33 | HG00099.hp1 HG01106.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-24-6957_-24-6956i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACAC others(27): Show |
11 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(8): Show | 11 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACGT others(27): Show |
7 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0001g0035others(4): Show | 7 | HG00280.hp1 HG02004.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(36): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACGT others(53): Show |
1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACGT others(55): Show |
2 | a0001c0003t0001g0054a0001c0003t0001g0055 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-24-6955_-24-6954i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACGT others(107): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(116): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATACGT others(55): Show |
1 | a0001c0003t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-24-6955_-24-6954i others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAC others(29): Show |
18 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24-6953_-24-6952i others(38): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAC others(29): Show |
1 | a0003c0005t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-24-6953_-24-6952i others(38): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(31): Show |
1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(40): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(17): Show |
5 | a0001c0001t0001g0235a0001c0001t0001g0328a0001c0001t0001g0330others(2): Show | 5 | HG01891.hp1 HG02257.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-6951_-24-6950i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(3): Show |
4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6951_-24-6950i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(31): Show |
1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-24-6951_-24-6950i others(40): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(52): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(19): Show |
69 | a0001c0001t0001g0378a0001c0001t0002g0372a0001c0001t0002g0373others(66): Show | 69 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(45): Show |
2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(71): Show |
21 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(80): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(97): Show |
1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(106): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(68): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(73): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | NA18982.hp2 NA18995.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(56): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(73): Show |
1 | a0001c0006t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(5): Show |
65 | a0001c0001t0001g0004a0001c0001t0001g0231a0001c0001t0001g0232others(62): Show | 65 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(83): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(92): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(53): Show |
25 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(62): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366125
|
A | ATATATAT others(93): Show |
1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-24-6945_-24-6944i others(102): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366125 | |||||
| chr2:241366127
|
A | ACGTATAT others(25): Show |
1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-24-6957_-24-6956i others(34): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366127 | ||||||
| chr2:241366127
|
A | ATATATAT others(17): Show |
9 | a0005c0008t0001g0144a0005c0008t0001g0148a0005c0008t0001g0150others(6): Show | 9 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-24-6949_-24-6948i others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366127 | |||||
| chr2:241366127
|
A | ATATATAT others(3): Show |
1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366127 | |||||
| chr2:241366129
|
A | ATATATAC others(15): Show |
1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366129 | |||||
| chr2:241366130
|
T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6954T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366130 | ||||||
| chr2:241366131
|
A | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6953A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366131 | ||||||
| chr2:241366133
|
A | ATACATAT others(73): Show |
1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-24-6949_-24-6948i others(82): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241366133 | |||||
| chr2:241366138
|
T | C | 50 | a0001c0001t0001g0378a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-24-6946T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366138 | ||||||
| chr2:241366140
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366140 | ||||||
| chr2:241366142
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6942C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366142 | ||||||
| chr2:241366146
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6938C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366146 | ||||||
| chr2:241366148
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6936C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366148 | ||||||
| chr2:241366157
|
T | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6927T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366157 | ||||||
| chr2:241366158
|
TTCTTCCT others(3444): Show |
T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-6925_-24-3475d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366158 | ||||||
| chr2:241366294
|
C | T | 1 | a0003c0005t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-24-6790C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366294 | ||||||
| chr2:241366360
|
T | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-6724T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366360 | ||||||
| chr2:241366440
|
A | G | 1 | a0005c0008t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-24-6644A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241366440 | ||||||
| chr2:241367201
|
G | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-5883G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241367201 | ||||||
| chr2:241367633
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-24-5451G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241367633 | ||||||
| chr2:241367875
|
C | CT | 14 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0125others(11): Show | 14 | HG01099.hp2 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-24-5198dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241367875 | |||||
| chr2:241368048
|
CATT | C | 35 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-5033_-24-5031d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241368048 | |||||
| chr2:241368188
|
G | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-4896G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368188 | ||||||
| chr2:241368237
|
G | A | 1 | a0003c0005t0001g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-24-4847G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368237 | ||||||
| chr2:241368409
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-24-4675G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368409 | ||||||
| chr2:241368413
|
C | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-24-4671C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368413 | ||||||
| chr2:241368547
|
C | T | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-4537C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368547 | ||||||
| chr2:241368611
|
G | A | 1 | a0001c0001t0009g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-4473G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368611 | ||||||
| chr2:241368624
|
A | T | 288 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-24-4460A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368624 | ||||||
| chr2:241368633
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-4451A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368633 | ||||||
| chr2:241368700
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-4384A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368700 | ||||||
| chr2:241368889
|
A | C | 1 | a0001c0003t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-24-4195A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241368889 | ||||||
| chr2:241369126
|
G | A | 1 | a0001c0006t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-24-3958G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369126 | ||||||
| chr2:241369202
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24-3882G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369202 | ||||||
| chr2:241369210
|
GTTTT | G | 5 | a0003c0005t0001g0008a0003c0005t0001g0040a0003c0005t0001g0052others(2): Show | 5 | HG00099.hp1 HG01123.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3871_-24-3868d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241369210 | |||||
| chr2:241369234
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24-3850T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369234 | ||||||
| chr2:241369397
|
CCTT | C | 35 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-3684_-24-3682d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241369397 | |||||
| chr2:241369571
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-24-3513A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369571 | ||||||
| chr2:241369612
|
T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3472T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369612 | ||||||
| chr2:241369614
|
T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3470T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369614 | ||||||
| chr2:241369617
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3467A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369617 | ||||||
| chr2:241369625
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3459C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369625 | ||||||
| chr2:241369626
|
T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3458T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369626 | ||||||
| chr2:241369629
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3455A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369629 | ||||||
| chr2:241369630
|
G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3454G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369630 | ||||||
| chr2:241369631
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3453A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369631 | ||||||
| chr2:241369633
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3451A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369633 | ||||||
| chr2:241369639
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3445A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369639 | ||||||
| chr2:241369647
|
T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3437T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369647 | ||||||
| chr2:241369652
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3432C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369652 | ||||||
| chr2:241369654
|
G | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3430G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369654 | ||||||
| chr2:241369655
|
T | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3429T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369655 | ||||||
| chr2:241369656
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3428A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369656 | ||||||
| chr2:241369658
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3426A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369658 | ||||||
| chr2:241369662
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3422A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369662 | ||||||
| chr2:241369671
|
A | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24-3413A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369671 | ||||||
| chr2:241369721
|
G | A | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-3363G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369721 | ||||||
| chr2:241369803
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-24-3281T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369803 | ||||||
| chr2:241369841
|
T | C | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-24-3243T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369841 | ||||||
| chr2:241369998
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-3086A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241369998 | ||||||
| chr2:241370375
|
C | T | 48 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-24-2709C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370375 | ||||||
| chr2:241370703
|
A | G | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-24-2381A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370703 | ||||||
| chr2:241370759
|
T | C | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-24-2325T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370759 | ||||||
| chr2:241370846
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-24-2238A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370846 | ||||||
| chr2:241370896
|
T | C | 4 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | NA18953.hp1 NA19000.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2188T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241370896 | ||||||
| chr2:241371006
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-24-2078G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371006 | ||||||
| chr2:241371011
|
G | A | 4 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(1): Show | 4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-2073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371011 | ||||||
| chr2:241371040
|
G | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-2044G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371040 | ||||||
| chr2:241371208
|
G | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-24-1876G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371208 | ||||||
| chr2:241371438
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-24-1646G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371438 | ||||||
| chr2:241371479
|
G | A | 1 | a0001c0004t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-24-1605G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371479 | ||||||
| chr2:241371562
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-24-1522C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371562 | ||||||
| chr2:241371579
|
C | T | 10 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-1505C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371579 | ||||||
| chr2:241371713
|
G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24-1371G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241371713 | ||||||
| chr2:241372090
|
CAT | C | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-24-992_-24-991del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241372090 | |||||
| chr2:241372094
|
G | A | 5 | a0006c0009t0001g0183a0006c0009t0001g0184a0006c0009t0001g0185others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-990G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372094 | ||||||
| chr2:241372273
|
G | T | 3 | a0001c0004t0001g0161a0001c0004t0001g0162a0001c0004t0001g0163 | 3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-24-811G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372273 | ||||||
| chr2:241372430
|
C | T | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-24-654C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372430 | ||||||
| chr2:241372601
|
G | A | 35 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-24-483G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372601 | ||||||
| chr2:241372717
|
G | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-24-367G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372717 | ||||||
| chr2:241372731
|
G | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-353G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372731 | ||||||
| chr2:241372937
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-24-147A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372937 | ||||||
| chr2:241372938
|
C | CT | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-24-143dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241372938 | |||||
| chr2:241372962
|
C | T | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-24-122C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372962 | ||||||
| chr2:241372995
|
C | T | 1 | a0003c0005t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-24-89C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241372995 | ||||||
| chr2:241373044
|
T | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-40T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241373044 | ||||||
| chr2:241373052
|
C | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-24-32C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | chr2 | 241373052 | ||||||
| chr2:241373062
|
G | GT | 108 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0092others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
splice_region_variant&intron_variant | LOW | c.-24-9dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 241373062 | |||||
| chr2:241373506
|
G | A | 1 | a0004c0007t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.183+216G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373506 | ||||||
| chr2:241373642
|
G | A | 1 | a0001c0006t0001g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.183+352G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373642 | ||||||
| chr2:241373948
|
A | G | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.183+658A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241373948 | ||||||
| chr2:241374043
|
T | C | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.183+753T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374043 | ||||||
| chr2:241374229
|
C | T | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+939C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374229 | ||||||
| chr2:241374714
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+1424T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374714 | ||||||
| chr2:241374745
|
G | A | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+1455G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374745 | ||||||
| chr2:241374814
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+1524T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374814 | ||||||
| chr2:241374858
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.183+1568G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374858 | ||||||
| chr2:241374971
|
G | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+1681G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241374971 | ||||||
| chr2:241375092
|
G | A | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.183+1802G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375092 | ||||||
| chr2:241375197
|
C | T | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+1907C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375197 | ||||||
| chr2:241375408
|
C | CT | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2128dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241375408 | |||||
| chr2:241375513
|
C | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+2223C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375513 | ||||||
| chr2:241375608
|
A | G | 4 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0004t0001g0171others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+2318A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375608 | ||||||
| chr2:241375777
|
G | T | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+2487G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241375777 | ||||||
| chr2:241376025
|
A | C | 1 | a0003c0005t0001g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.183+2735A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376025 | ||||||
| chr2:241376028
|
A | G | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+2738A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376028 | ||||||
| chr2:241376191
|
A | G | 5 | a0001c0004t0001g0361a0001c0004t0001g0362a0001c0010t0001g0363others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+2901A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376191 | ||||||
| chr2:241376221
|
G | A | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+2931G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376221 | ||||||
| chr2:241376404
|
A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+3114A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376404 | ||||||
| chr2:241376499
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.183+3209T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376499 | ||||||
| chr2:241376526
|
TC | T | 288 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.183+3241delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241376526 | |||||
| chr2:241376617
|
G | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+3327G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376617 | ||||||
| chr2:241376646
|
G | T | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+3356G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376646 | ||||||
| chr2:241376659
|
C | T | 1 | a0003c0005t0001g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+3369C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376659 | ||||||
| chr2:241376672
|
C | T | 1 | a0001c0006t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.183+3382C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376672 | ||||||
| chr2:241376748
|
G | A | 3 | a0001c0004t0001g0161a0001c0004t0001g0162a0001c0004t0001g0163 | 3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+3458G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376748 | ||||||
| chr2:241376787
|
G | A | 3 | a0001c0001t0009g0104a0001c0011t0001g0107a0001c0011t0001g0108 | 3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.183+3497G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376787 | ||||||
| chr2:241376969
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+3679A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241376969 | ||||||
| chr2:241377097
|
C | T | 26 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+3807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377097 | ||||||
| chr2:241377194
|
G | A | 1 | a0020c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.183+3904G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377194 | ||||||
| chr2:241377333
|
CT | C | 69 | a0001c0001t0001g0270a0001c0001t0001g0378a0001c0003t0001g0007others(66): Show | 69 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.183+4062delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241377333 | |||||
| chr2:241377333
|
CTT | C | 29 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(26): Show | 29 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.183+4061_183+4062d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241377333 | |||||
| chr2:241377352
|
T | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4062T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377352 | ||||||
| chr2:241377379
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.183+4089G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377379 | ||||||
| chr2:241377428
|
G | A | 26 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+4138G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377428 | ||||||
| chr2:241377464
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4174C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377464 | ||||||
| chr2:241377498
|
C | T | 1 | a0001c0001t0002g0375 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.183+4208C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377498 | ||||||
| chr2:241377686
|
C | A | 1 | a0001c0001t0009g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.183+4396C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377686 | ||||||
| chr2:241377813
|
G | A | 2 | a0001c0001t0001g0158a0001c0004t0001g0157 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.183+4523G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377813 | ||||||
| chr2:241377830
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4540G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377830 | ||||||
| chr2:241377859
|
G | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0358 | 2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.183+4569G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377859 | ||||||
| chr2:241377864
|
A | G | 1 | a0004c0007t0001g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.183+4574A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377864 | ||||||
| chr2:241377892
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+4602C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241377892 | ||||||
| chr2:241378109
|
A | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+4819A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378109 | ||||||
| chr2:241378140
|
C | T | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+4850C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378140 | ||||||
| chr2:241378270
|
AT | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.183+4992delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378270 | |||||
| chr2:241378299
|
C | T | 2 | a0001c0006t0001g0242a0001c0006t0001g0243 | 2 | HG00621.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.183+5009C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378299 | ||||||
| chr2:241378300
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.183+5010G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378300 | ||||||
| chr2:241378362
|
C | G | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+5072C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378362 | ||||||
| chr2:241378416
|
A | ATTTTTTT others(2): Show |
85 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(82): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.183+5131_183+5139d others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | |||||
| chr2:241378416
|
A | ATTTTTTT others(3): Show |
105 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.183+5130_183+5139d others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | |||||
| chr2:241378416
|
A | ATTTTTTT others(4): Show |
84 | a0001c0001t0001g0004a0001c0001t0001g0234a0001c0001t0001g0235others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.183+5129_183+5139d others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | |||||
| chr2:241378416
|
A | ATTTTTTT others(5): Show |
17 | a0001c0001t0001g0158a0001c0001t0001g0239a0001c0001t0001g0298others(14): Show | 17 | HG01071.hp1 HG01175.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+5128_183+5139d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241378416 | |||||
| chr2:241378506
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.183+5216G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378506 | ||||||
| chr2:241378537
|
T | C | 291 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.183+5247T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378537 | ||||||
| chr2:241378558
|
G | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+5268G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378558 | ||||||
| chr2:241378874
|
T | A | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.183+5584T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241378874 | ||||||
| chr2:241379043
|
G | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+5753G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379043 | ||||||
| chr2:241379086
|
G | C | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+5796G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379086 | ||||||
| chr2:241379168
|
C | G | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+5878C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379168 | ||||||
| chr2:241379368
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+6078G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379368 | ||||||
| chr2:241379395
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.183+6105C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379395 | ||||||
| chr2:241379449
|
C | G | 1 | a0005c0008t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+6159C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379449 | ||||||
| chr2:241379774
|
A | G | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.183+6484A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241379774 | ||||||
| chr2:241380084
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+6794A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380084 | ||||||
| chr2:241380360
|
G | T | 18 | a0002c0002t0001g0338a0002c0002t0001g0340a0002c0002t0001g0341others(15): Show | 18 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.183+7070G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380360 | ||||||
| chr2:241380378
|
C | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+7088C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380378 | ||||||
| chr2:241380574
|
C | G | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+7284C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380574 | ||||||
| chr2:241380600
|
C | A | 1 | a0001c0006t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.183+7310C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380600 | ||||||
| chr2:241380661
|
A | G | 1 | a0001c0022t0001g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.183+7371A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380661 | ||||||
| chr2:241380690
|
ATATAT | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+7411_183+7415d others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241380690 | |||||
| chr2:241380878
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+7588C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380878 | ||||||
| chr2:241380906
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.183+7616G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241380906 | ||||||
| chr2:241381187
|
T | C | 2 | a0001c0003t0001g0060a0001c0003t0008g0061 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.183+7897T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381187 | ||||||
| chr2:241381235
|
C | T | 17 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(14): Show | 17 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+7945C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381235 | ||||||
| chr2:241381320
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0109 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+8030G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381320 | ||||||
| chr2:241381363
|
G | C | 1 | a0001c0004t0001g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.183+8073G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381363 | ||||||
| chr2:241381404
|
G | A | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.183+8114G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381404 | ||||||
| chr2:241381607
|
T | G | 2 | a0001c0004t0001g0359a0001c0004t0001g0360 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+8317T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381607 | ||||||
| chr2:241381611
|
G | A | 280 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.183+8321G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381611 | ||||||
| chr2:241381656
|
G | A | 5 | a0001c0003t0001g0034a0001c0003t0001g0035a0001c0003t0001g0037others(2): Show | 5 | HG03139.hp1 NA18972.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+8366G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381656 | ||||||
| chr2:241381658
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.183+8368A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381658 | ||||||
| chr2:241381668
|
G | A | 370 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(367): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.183+8378G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381668 | ||||||
| chr2:241381756
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.183+8466T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381756 | ||||||
| chr2:241381828
|
G | A | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.183+8538G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381828 | ||||||
| chr2:241381943
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+8653C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241381943 | ||||||
| chr2:241382170
|
A | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+8880A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382170 | ||||||
| chr2:241382185
|
G | A | 4 | a0005c0008t0001g0144a0005c0008t0001g0148a0005c0008t0001g0154others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+8895G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382185 | ||||||
| chr2:241382288
|
A | ATC | 44 | a0001c0001t0001g0004a0001c0001t0001g0231a0001c0001t0001g0234others(41): Show | 44 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.183+9000_183+9001d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382288 | |||||
| chr2:241382290
|
C | CAA | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9000_183+9001i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382290 | ||||||
| chr2:241382290
|
C | CTCT | 3 | a0001c0001t0001g0238a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG03688.hp1 NA18943.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.183+9001_183+9002i others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382290 | |||||
| chr2:241382291
|
T | TC | 38 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0232others(35): Show | 38 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+9001_183+9002i others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382291 | ||||||
| chr2:241382292
|
A | AT | 68 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0109others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.183+9022dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241382292 | |||||
| chr2:241382292
|
A | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0305a0001c0001t0001g0306others(1): Show | 4 | HG01070.hp2 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+9002A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382292 | ||||||
| chr2:241382292
|
A | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0202a0001c0001t0001g0204others(89): Show | 92 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.183+9002A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382292 | ||||||
| chr2:241382349
|
C | T | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+9059C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382349 | ||||||
| chr2:241382407
|
C | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9117C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382407 | ||||||
| chr2:241382410
|
A | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+9120A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382410 | ||||||
| chr2:241382475
|
G | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9185G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382475 | ||||||
| chr2:241382483
|
A | G | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9193A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382483 | ||||||
| chr2:241382768
|
C | T | 52 | a0001c0001t0001g0378a0001c0006t0001g0236a0001c0006t0001g0240others(49): Show | 52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.183+9478C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241382768 | ||||||
| chr2:241383015
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+9725G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383015 | ||||||
| chr2:241383163
|
C | T | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.183+9873C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383163 | ||||||
| chr2:241383171
|
G | A | 30 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.183+9881G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383171 | ||||||
| chr2:241383225
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9935C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383225 | ||||||
| chr2:241383236
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.183+9946C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383236 | ||||||
| chr2:241383252
|
A | G | 370 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(367): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.183+9962A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383252 | ||||||
| chr2:241383258
|
C | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+9968C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383258 | ||||||
| chr2:241383265
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(178): Show | 181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.183+9975T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383265 | ||||||
| chr2:241383337
|
A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+10047A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383337 | ||||||
| chr2:241383520
|
G | A | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+10230G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383520 | ||||||
| chr2:241383702
|
G | T | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+10412G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383702 | ||||||
| chr2:241383813
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.183+10523G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383813 | ||||||
| chr2:241383918
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0226a0001c0032t0001g0227 | 3 | HG03654.hp1 NA21309.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.183+10628C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383918 | ||||||
| chr2:241383938
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02056.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.183+10648G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241383938 | ||||||
| chr2:241384108
|
A | G | 10 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00639.hp2 HG01167.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+10818A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384108 | ||||||
| chr2:241384201
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+10911G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384201 | ||||||
| chr2:241384222
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+10932A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384222 | ||||||
| chr2:241384360
|
C | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+11070C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384360 | ||||||
| chr2:241384363
|
G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183+11073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384363 | ||||||
| chr2:241384487
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.183+11197G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384487 | ||||||
| chr2:241384524
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+11234C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384524 | ||||||
| chr2:241384583
|
C | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+11293C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384583 | ||||||
| chr2:241384931
|
A | G | 1 | a0001c0003t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.183+11641A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384931 | ||||||
| chr2:241384964
|
A | G | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.183+11674A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241384964 | ||||||
| chr2:241385272
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+11982A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385272 | ||||||
| chr2:241385345
|
A | C | 86 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.183+12055A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385345 | ||||||
| chr2:241385348
|
G | A | 86 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(83): Show | 86 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.183+12058G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385348 | ||||||
| chr2:241385356
|
T | C | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.183+12066T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385356 | ||||||
| chr2:241385472
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+12182G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385472 | ||||||
| chr2:241385669
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.183+12379G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385669 | ||||||
| chr2:241385685
|
A | G | 1 | a0002c0002t0001g0261 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.183+12395A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385685 | ||||||
| chr2:241385772
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+12482T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385772 | ||||||
| chr2:241385966
|
T | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+12676T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241385966 | ||||||
| chr2:241386385
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+13095C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386385 | ||||||
| chr2:241386408
|
A | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.183+13118A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386408 | ||||||
| chr2:241386432
|
T | C | 3 | a0002c0002t0001g0335a0002c0002t0001g0336a0002c0002t0001g0353 | 3 | NA18952.hp2 NA18963.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.183+13142T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386432 | ||||||
| chr2:241386497
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0109 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+13207C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386497 | ||||||
| chr2:241386560
|
G | C | 7 | a0001c0001t0001g0270a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | NA18946.hp2 NA18949.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+13270G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386560 | ||||||
| chr2:241386565
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.183+13275G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386565 | ||||||
| chr2:241386654
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+13364C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386654 | ||||||
| chr2:241386908
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.183+13618A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386908 | ||||||
| chr2:241386935
|
A | G | 1 | a0001c0003t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.183+13645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241386935 | ||||||
| chr2:241387236
|
C | T | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.183+13946C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387236 | ||||||
| chr2:241387373
|
T | A | 1 | a0003c0005t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+14083T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387373 | ||||||
| chr2:241387454
|
C | T | 324 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.183+14164C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387454 | ||||||
| chr2:241387532
|
G | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG00621.hp1 HG02273.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.183+14242G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387532 | ||||||
| chr2:241387570
|
G | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.183+14280G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387570 | ||||||
| chr2:241387606
|
A | G | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.183+14316A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387606 | ||||||
| chr2:241387661
|
T | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+14371T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387661 | ||||||
| chr2:241387705
|
A | T | 1 | a0002c0002t0001g0352 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.183+14415A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387705 | ||||||
| chr2:241387748
|
G | A | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.183+14458G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387748 | ||||||
| chr2:241387790
|
CA | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(173): Show | 176 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.183+14519delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241387790 | |||||
| chr2:241387803
|
A | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+14513A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387803 | ||||||
| chr2:241387809
|
A | G | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183+14519A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387809 | ||||||
| chr2:241387878
|
C | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+14588C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241387878 | ||||||
| chr2:241388234
|
T | C | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+14944T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388234 | ||||||
| chr2:241388292
|
G | A | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+15002G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388292 | ||||||
| chr2:241388318
|
A | C | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.183+15028A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388318 | ||||||
| chr2:241388399
|
C | T | 2 | a0003c0005t0001g0198a0003c0005t0001g0199 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.183+15109C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388399 | ||||||
| chr2:241388558
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.183+15268A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388558 | ||||||
| chr2:241388662
|
C | T | 1 | a0001c0011t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-15166C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388662 | ||||||
| chr2:241388663
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-15165G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388663 | ||||||
| chr2:241388840
|
C | G | 4 | a0003c0005t0001g0043a0003c0005t0001g0044a0003c0005t0001g0045others(1): Show | 4 | NA18953.hp2 NA18963.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-14988C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388840 | ||||||
| chr2:241388973
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.184-14855T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388973 | ||||||
| chr2:241388997
|
G | A | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184-14831G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241388997 | ||||||
| chr2:241389270
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.184-14558C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241389270 | ||||||
| chr2:241389991
|
A | G | 16 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(13): Show | 16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.184-13837A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241389991 | ||||||
| chr2:241390039
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.184-13789A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390039 | ||||||
| chr2:241390086
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-13742C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390086 | ||||||
| chr2:241390138
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.184-13690G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390138 | ||||||
| chr2:241390174
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.184-13654C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390174 | ||||||
| chr2:241390402
|
A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.184-13426A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390402 | ||||||
| chr2:241390663
|
A | G | 4 | a0003c0005t0001g0043a0003c0005t0001g0044a0003c0005t0001g0045others(1): Show | 4 | NA18953.hp2 NA18963.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-13165A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390663 | ||||||
| chr2:241390777
|
G | T | 292 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0158others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.184-13051G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390777 | ||||||
| chr2:241390919
|
T | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-12909T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390919 | ||||||
| chr2:241390981
|
C | G | 1 | a0002c0002t0001g0351 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.184-12847C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241390981 | ||||||
| chr2:241391336
|
A | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-12492A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391336 | ||||||
| chr2:241391700
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-12128C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391700 | ||||||
| chr2:241391852
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.184-11976G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391852 | ||||||
| chr2:241391860
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-11968G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391860 | ||||||
| chr2:241391861
|
C | A | 1 | a0001c0022t0001g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.184-11967C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391861 | ||||||
| chr2:241391907
|
T | G | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.184-11921T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241391907 | ||||||
| chr2:241392200
|
C | T | 4 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-11628C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392200 | ||||||
| chr2:241392272
|
G | A | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184-11556G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392272 | ||||||
| chr2:241392796
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-11032A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392796 | ||||||
| chr2:241392842
|
C | T | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-10986C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241392842 | ||||||
| chr2:241392949
|
G | GA | 30 | a0001c0001t0001g0209a0003c0005t0001g0008a0003c0005t0001g0039others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.184-10868dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241392949 | |||||
| chr2:241393023
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.184-10805T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393023 | ||||||
| chr2:241393180
|
C | T | 42 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0237others(39): Show | 42 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.184-10648C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393180 | ||||||
| chr2:241393300
|
G | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-10528G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393300 | ||||||
| chr2:241393300
|
G | T | 33 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(30): Show | 33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.184-10528G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393300 | ||||||
| chr2:241393340
|
A | G | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.184-10488A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393340 | ||||||
| chr2:241393575
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.184-10253C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393575 | ||||||
| chr2:241393661
|
A | G | 1 | a0001c0004t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-10167A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393661 | ||||||
| chr2:241393709
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.184-10119A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393709 | ||||||
| chr2:241393775
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-10053A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393775 | ||||||
| chr2:241393999
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-9829G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241393999 | ||||||
| chr2:241394055
|
T | C | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-9773T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394055 | ||||||
| chr2:241394058
|
A | C | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.184-9770A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394058 | ||||||
| chr2:241394171
|
G | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-9657G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394171 | ||||||
| chr2:241394387
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.184-9441G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394387 | ||||||
| chr2:241394474
|
C | A | 99 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.184-9354C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394474 | ||||||
| chr2:241394517
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-9311C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394517 | ||||||
| chr2:241394517
|
C | CA | 31 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0134others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.184-9294dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241394517 | |||||
| chr2:241394517
|
CA | C | 52 | a0001c0001t0001g0201a0001c0001t0001g0303a0001c0001t0001g0377others(49): Show | 52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.184-9294delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241394517 | |||||
| chr2:241394605
|
C | T | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-9223C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394605 | ||||||
| chr2:241394920
|
G | A | 110 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.184-8908G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241394920 | ||||||
| chr2:241395034
|
G | T | 1 | a0001c0006t0001g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.184-8794G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395034 | ||||||
| chr2:241395044
|
A | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-8784A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395044 | ||||||
| chr2:241395080
|
G | A | 1 | a0003c0005t0001g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.184-8748G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395080 | ||||||
| chr2:241395093
|
A | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.184-8735A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395093 | ||||||
| chr2:241395187
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.184-8641C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395187 | ||||||
| chr2:241395193
|
G | T | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.184-8635G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395193 | ||||||
| chr2:241395220
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184-8608G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395220 | ||||||
| chr2:241395342
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.184-8486A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395342 | ||||||
| chr2:241395550
|
C | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-8278C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395550 | ||||||
| chr2:241395760
|
A | G | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.184-8068A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395760 | ||||||
| chr2:241395928
|
G | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-7900G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241395928 | ||||||
| chr2:241396009
|
T | C | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-7819T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396009 | ||||||
| chr2:241396044
|
T | A | 1 | a0001c0001t0001g0283 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.184-7784T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396044 | ||||||
| chr2:241396095
|
G | C | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-7733G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396095 | ||||||
| chr2:241396270
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.184-7558A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396270 | ||||||
| chr2:241396345
|
A | C | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-7483A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396345 | ||||||
| chr2:241396425
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-7403A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396425 | ||||||
| chr2:241396507
|
T | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG00733.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.184-7321T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396507 | ||||||
| chr2:241396517
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.184-7311G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396517 | ||||||
| chr2:241396587
|
T | G | 2 | a0001c0006t0001g0244a0001c0006t0001g0245 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.184-7241T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396587 | ||||||
| chr2:241396625
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-7203C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396625 | ||||||
| chr2:241396884
|
C | T | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.184-6944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396884 | ||||||
| chr2:241396958
|
G | GATTAAGA others(11): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-6867_184-6850d others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241396958 | |||||
| chr2:241396984
|
G | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-6844G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396984 | ||||||
| chr2:241396996
|
A | G | 1 | a0001c0004t0001g0179 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.184-6832A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241396996 | ||||||
| chr2:241397030
|
T | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-6798T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397030 | ||||||
| chr2:241397143
|
G | A | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-6685G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397143 | ||||||
| chr2:241397192
|
G | C | 1 | a0003c0005t0001g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.184-6636G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397192 | ||||||
| chr2:241397199
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.184-6629G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397199 | ||||||
| chr2:241397441
|
C | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.184-6387C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397441 | ||||||
| chr2:241397791
|
C | G | 2 | a0003c0005t0001g0047a0003c0005t0001g0048 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.184-6037C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397791 | ||||||
| chr2:241397831
|
C | CT | 53 | a0001c0001t0001g0134a0001c0001t0001g0204a0001c0001t0001g0217others(50): Show | 53 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.184-5979dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | |||||
| chr2:241397831
|
C | CTT | 28 | a0002c0002t0001g0343a0002c0002t0001g0357a0003c0005t0001g0008others(25): Show | 28 | HG00099.hp1 HG01123.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.184-5980_184-5979d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | |||||
| chr2:241397831
|
CT | C | 79 | a0001c0001t0001g0158a0001c0001t0001g0366a0001c0001t0001g0367others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-5979delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397831 | |||||
| chr2:241397868
|
C | T | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.184-5960C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397868 | ||||||
| chr2:241397884
|
C | T | 17 | a0001c0004t0001g0165a0001c0004t0001g0166a0001c0004t0001g0167others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.184-5944C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397884 | ||||||
| chr2:241397974
|
C | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-5854C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241397974 | ||||||
| chr2:241397996
|
A | AT | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-5824dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241397996 | |||||
| chr2:241398021
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184-5807T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398021 | ||||||
| chr2:241398036
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.184-5792T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398036 | ||||||
| chr2:241398218
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.184-5610A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398218 | ||||||
| chr2:241398233
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-5595T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398233 | ||||||
| chr2:241398245
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.184-5583C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398245 | ||||||
| chr2:241398268
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184-5560C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398268 | ||||||
| chr2:241398307
|
G | C | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.184-5521G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398307 | ||||||
| chr2:241398428
|
G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.184-5400G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398428 | ||||||
| chr2:241398572
|
C | CT | 40 | a0001c0001t0001g0005a0002c0002t0001g0200a0002c0002t0001g0253others(37): Show | 40 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.184-5241dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398572 | |||||
| chr2:241398572
|
C | CTT | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.184-5242_184-5241d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398572 | |||||
| chr2:241398666
|
T | C | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184-5162T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398666 | ||||||
| chr2:241398812
|
G | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-5016G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398812 | ||||||
| chr2:241398838
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.184-4990G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398838 | ||||||
| chr2:241398876
|
C | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.184-4952C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398876 | ||||||
| chr2:241398899
|
A | G | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-4929A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241398899 | ||||||
| chr2:241398980
|
ATAC | A | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184-4846_184-4844d others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241398980 | |||||
| chr2:241399220
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.184-4608C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399220 | ||||||
| chr2:241399394
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.184-4434T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399394 | ||||||
| chr2:241399431
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.184-4397A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399431 | ||||||
| chr2:241399733
|
G | T | 1 | a0001c0003t0001g0026 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-4095G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399733 | ||||||
| chr2:241399802
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-4026G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241399802 | ||||||
| chr2:241399988
|
CTG | C | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.184-3837_184-3836d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241399988 | |||||
| chr2:241400027
|
G | A | 2 | a0001c0004t0001g0359a0001c0004t0001g0360 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-3801G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400027 | ||||||
| chr2:241400059
|
G | C | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.184-3769G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400059 | ||||||
| chr2:241400120
|
G | T | 1 | a0001c0006t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.184-3708G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400120 | ||||||
| chr2:241400170
|
G | C | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.184-3658G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400170 | ||||||
| chr2:241400229
|
A | AAG | 222 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(219): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.184-3598_184-3597d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241400229 | |||||
| chr2:241400234
|
T | G | 291 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.184-3594T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400234 | ||||||
| chr2:241400241
|
A | G | 85 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(82): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.184-3587A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400241 | ||||||
| chr2:241400321
|
G | C | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-3507G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241400321 | ||||||
| chr2:241401125
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2703G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401125 | ||||||
| chr2:241401259
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-2569C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401259 | ||||||
| chr2:241401573
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-2255G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401573 | ||||||
| chr2:241401662
|
T | A | 1 | a0001c0003t0001g0026 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.184-2166T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401662 | ||||||
| chr2:241401806
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.184-2022C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401806 | ||||||
| chr2:241401807
|
G | A | 1 | a0020c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.184-2021G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401807 | ||||||
| chr2:241401818
|
C | CTT | 291 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.184-2010_184-2009i others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401818 | ||||||
| chr2:241401844
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.184-1984G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241401844 | ||||||
| chr2:241402021
|
C | T | 2 | a0001c0004t0001g0359a0001c0004t0001g0360 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402021 | ||||||
| chr2:241402091
|
A | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-1737A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402091 | ||||||
| chr2:241402159
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.184-1669G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402159 | ||||||
| chr2:241402485
|
G | A | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.184-1343G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402485 | ||||||
| chr2:241402834
|
A | ATT | 7 | a0001c0001t0001g0283a0001c0001t0001g0287a0001c0001t0001g0308others(4): Show | 7 | HG00099.hp1 HG01993.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-992_184-991dup others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402834 | |||||
| chr2:241402836
|
T | TTATA | 3 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0141 | 3 | HG04228.hp1 HG04228.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.184-950_184-947dup others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0135a0001c0001t0001g0188a0001c0011t0001g0108 | 3 | HG00544.hp1 HG00558.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.184-954_184-947dup others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0218a0011c0020t0001g0155 | 3 | HG00323.hp1 HG02135.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.184-956_184-947dup others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTATATAT others(5): Show |
1 | a0001c0019t0001g0111 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.184-958_184-947dup others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTATATAT others(9): Show |
1 | a0001c0022t0001g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.184-962_184-947dup others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTTTATAT others(5): Show |
2 | a0001c0001t0001g0204a0003c0005t0001g0051 | 2 | HG03669.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.184-991_184-990ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
T | TTTTATAT others(13): Show |
3 | a0003c0005t0001g0041a0003c0005t0001g0042a0016c0030t0001g0006 | 3 | HG02486.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.184-991_184-990ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTA | T | 11 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG00408.hp2 HG00733.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-948_184-947del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0223a0001c0004t0001g0164a0003c0005t0001g0057 | 3 | HG01123.hp1 HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.184-956_184-947del others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTATATAT others(5): Show |
T | 9 | a0001c0001t0001g0368a0001c0004t0001g0162a0001c0004t0001g0163others(6): Show | 9 | HG00642.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-958_184-947del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTATATAT others(11): Show |
T | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.184-964_184-947del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTATATAT others(13): Show |
T | 11 | a0001c0003t0001g0010a0001c0003t0001g0016a0001c0003t0001g0020others(8): Show | 11 | HG01255.hp2 HG02129.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-966_184-947del others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402836
|
TTATATAT others(17): Show |
T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-970_184-947del others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402836 | |||||
| chr2:241402838
|
A | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.184-990A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402838 | ||||||
| chr2:241402840
|
A | T | 6 | a0001c0001t0001g0297a0001c0001t0001g0309a0001c0001t0001g0319others(3): Show | 6 | HG00408.hp2 HG00733.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-988A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402840 | ||||||
| chr2:241402844
|
A | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.184-984A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402844 | ||||||
| chr2:241402844
|
A | T | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.184-984A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402844 | ||||||
| chr2:241402845
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402845 | |||||
| chr2:241402845
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0084 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.184-964_184-963ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402845 | |||||
| chr2:241402846
|
A | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-982A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402846 | ||||||
| chr2:241402847
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0079 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.184-968_184-967ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402847 | |||||
| chr2:241402847
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0066 | 2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.184-966_184-965ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402847 | |||||
| chr2:241402848
|
A | T | 2 | a0001c0004t0001g0164a0003c0005t0001g0057 | 2 | HG01123.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.184-980A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402848 | ||||||
| chr2:241402849
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402849 | |||||
| chr2:241402850
|
A | T | 8 | a0001c0004t0001g0162a0001c0004t0001g0163a0001c0004t0001g0168others(5): Show | 8 | HG00642.hp1 HG01169.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-978A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402850 | ||||||
| chr2:241402853
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-966_184-965ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402853 | |||||
| chr2:241402856
|
A | T | 1 | a0001c0003t0001g0011 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.184-972A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402856 | ||||||
| chr2:241402858
|
A | T | 11 | a0001c0003t0001g0010a0001c0003t0001g0016a0001c0003t0001g0020others(8): Show | 11 | HG01255.hp2 HG02129.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-970A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402858 | ||||||
| chr2:241402858
|
ATATATAT others(21): Show |
A | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.184-968_184-941del others(28): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402858 | |||||
| chr2:241402859
|
TATATATA others(10): Show |
T | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.184-968_184-952del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402859 | ||||||
| chr2:241402859
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.184-968_184-950del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402859 | ||||||
| chr2:241402860
|
A | C | 35 | a0002c0002t0001g0200a0002c0002t0001g0254a0002c0002t0001g0256others(32): Show | 35 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.184-968A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402860 | ||||||
| chr2:241402860
|
ATATATAT others(14): Show |
A | 2 | a0008c0028t0001g0018a0020c0031t0001g0019 | 2 | HG02055.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.184-966_184-946del others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402860 | |||||
| chr2:241402861
|
TATATATA others(12): Show |
T | 2 | a0001c0003t0001g0017a0001c0003t0001g0037 | 2 | HG00609.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.184-966_184-948del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402861 | ||||||
| chr2:241402862
|
A | C | 1 | a0002c0002t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.184-966A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402862 | ||||||
| chr2:241402862
|
ATATATAT others(12): Show |
A | 2 | a0001c0003t0001g0023a0001c0003t0001g0060 | 2 | HG01192.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.184-964_184-946del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402862 | |||||
| chr2:241402862
|
ATATATAT others(13): Show |
A | 9 | a0001c0001t0001g0123a0001c0003t0001g0007a0001c0003t0001g0022others(6): Show | 9 | HG00280.hp1 HG01106.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-964_184-945del others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402862 | |||||
| chr2:241402863
|
T | C | 21 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.184-965T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402863 | ||||||
| chr2:241402863
|
TATATATA others(10): Show |
T | 3 | a0001c0001t0001g0322a0001c0001t0001g0378a0001c0003t0001g0009 | 3 | HG02083.hp1 HG02258.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.184-964_184-948del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402863 | ||||||
| chr2:241402864
|
ATATATAT others(11): Show |
A | 5 | a0001c0003t0001g0012a0001c0003t0001g0013a0001c0003t0001g0014others(2): Show | 5 | HG03486.hp1 NA18955.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-962_184-945del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402864 | |||||
| chr2:241402864
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0269a0005c0008t0001g0147 | 2 | HG02451.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.184-962_184-944del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402864 | |||||
| chr2:241402865
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.184-963T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402865 | ||||||
| chr2:241402866
|
ATATATAT others(9): Show |
A | 2 | a0005c0008t0001g0152a0005c0008t0001g0153 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.184-960_184-945del others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402866 | |||||
| chr2:241402866
|
ATATATAT others(10): Show |
A | 1 | a0005c0008t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.184-960_184-944del others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402866 | |||||
| chr2:241402867
|
T | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0091 | 2 | HG02071.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.184-961T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | ||||||
| chr2:241402867
|
TATATATA others(4): Show |
T | 5 | a0003c0005t0001g0192a0003c0005t0001g0195a0003c0005t0001g0196others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-960_184-950del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | ||||||
| chr2:241402867
|
TATATATA others(6): Show |
T | 1 | a0006c0009t0001g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.184-960_184-948del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402867 | ||||||
| chr2:241402868
|
ATATATAT others(6): Show |
A | 1 | a0001c0004t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.184-958_184-946del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | |||||
| chr2:241402868
|
ATATATAT others(7): Show |
A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.184-958_184-945del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | |||||
| chr2:241402868
|
ATATATAT others(8): Show |
A | 1 | a0001c0003t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.184-958_184-944del others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | |||||
| chr2:241402868
|
ATATATAT others(9): Show |
A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.184-958_184-943del others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | |||||
| chr2:241402868
|
ATATATAT others(12): Show |
A | 2 | a0001c0006t0001g0246a0001c0006t0001g0251 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.184-958_184-940del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402868 | |||||
| chr2:241402869
|
TATATATA others(4): Show |
T | 2 | a0003c0005t0001g0046a0003c0005t0001g0193 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.184-958_184-948del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402869 | ||||||
| chr2:241402870
|
ATATATAT others(4): Show |
A | 5 | a0001c0025t0001g0160a0003c0005t0001g0197a0006c0009t0001g0183others(2): Show | 5 | HG01123.hp2 HG01168.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-956_184-946del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | |||||
| chr2:241402870
|
ATATATAT others(5): Show |
A | 4 | a0001c0004t0001g0166a0001c0004t0001g0167a0001c0004t0001g0179others(1): Show | 4 | HG01433.hp2 HG03017.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-956_184-945del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | |||||
| chr2:241402870
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.184-956_184-943del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | |||||
| chr2:241402870
|
ATATATAT others(11): Show |
A | 1 | a0001c0006t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.184-956_184-939del others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | |||||
| chr2:241402870
|
ATATATAT others(12): Show |
A | 3 | a0001c0006t0001g0236a0001c0006t0001g0247a0001c0006t0001g0248 | 3 | NA18984.hp2 NA19077.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.184-956_184-938del others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402870 | |||||
| chr2:241402872
|
A | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.184-956A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402872 | ||||||
| chr2:241402872
|
ATATATAT others(4): Show |
A | 2 | a0001c0004t0001g0177a0001c0004t0001g0181 | 2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.184-954_184-944del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | |||||
| chr2:241402872
|
ATATATAT others(5): Show |
A | 2 | a0001c0004t0001g0178a0001c0004t0001g0180 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.184-954_184-943del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | |||||
| chr2:241402872
|
ATATATAT others(7): Show |
A | 2 | a0001c0006t0001g0241a0001c0006t0001g0250 | 2 | HG02056.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.184-954_184-941del others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402872 | |||||
| chr2:241402874
|
ATATATAT others(4): Show |
A | 2 | a0002c0002t0001g0259a0002c0002t0001g0358 | 2 | HG02080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.184-952_184-942del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | |||||
| chr2:241402874
|
ATATATAT others(5): Show |
A | 9 | a0002c0002t0001g0256a0002c0002t0001g0257a0002c0002t0001g0258others(6): Show | 9 | HG00609.hp2 NA18942.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-952_184-941del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | |||||
| chr2:241402874
|
ATATATAT others(6): Show |
A | 2 | a0001c0006t0001g0244a0002c0002t0001g0200 | 2 | HG00408.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.184-952_184-940del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | |||||
| chr2:241402874
|
ATATATAT others(8): Show |
A | 1 | a0001c0006t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.184-952_184-938del others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402874 | |||||
| chr2:241402875
|
TATA | T | 3 | a0001c0001t0001g0306a0001c0001t0001g0318a0008c0021t0003g0334 | 3 | HG00140.hp2 HG01070.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.184-952_184-950del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402875 | ||||||
| chr2:241402876
|
A | T | 5 | a0001c0001t0001g0305a0001c0001t0001g0307a0001c0004t0001g0157others(2): Show | 5 | HG00738.hp1 HG01516.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-952A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402876 | ||||||
| chr2:241402876
|
ATATATTT others(3): Show |
A | 3 | a0002c0002t0001g0253a0002c0002t0001g0260a0017c0017t0001g0255 | 3 | HG00597.hp1 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.184-950_184-941del others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | |||||
| chr2:241402876
|
ATATATTT others(4): Show |
A | 3 | a0002c0002t0001g0254a0002c0002t0001g0261a0002c0002t0001g0342 | 3 | HG00639.hp1 HG02293.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.184-950_184-940del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | |||||
| chr2:241402876
|
ATATATTT others(5): Show |
A | 14 | a0002c0002t0001g0335a0002c0002t0001g0340a0002c0002t0001g0341others(11): Show | 14 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.184-950_184-939del others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | |||||
| chr2:241402876
|
ATATATTT others(6): Show |
A | 2 | a0001c0006t0001g0245a0002c0002t0001g0345 | 2 | HG00597.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.184-950_184-938del others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402876 | |||||
| chr2:241402878
|
A | T | 21 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0216others(18): Show | 21 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.184-950A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402878 | ||||||
| chr2:241402878
|
ATAT | A | 7 | a0001c0001t0001g0202a0001c0001t0001g0267a0001c0001t0001g0279others(4): Show | 7 | NA18960.hp2 NA18971.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-948_184-946del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402878 | |||||
| chr2:241402878
|
ATATTTTT others(4): Show |
A | 4 | a0001c0006t0001g0242a0002c0002t0001g0338a0002c0002t0001g0343others(1): Show | 4 | HG00621.hp2 HG01175.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-948_184-938del others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402878 | |||||
| chr2:241402879
|
TA | T | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0004g0265others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-948delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402879 | ||||||
| chr2:241402880
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0213 | 2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0303 | 2 | HG01891.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(27): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0221a0001c0001t0001g0224 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(19): Show |
1 | a0004c0007t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(26): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0211 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0091 | 2 | HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(17): Show |
1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0206 | 2 | HG03942.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0209 | 2 | NA18971.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(10): Show |
8 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0075others(5): Show | 8 | HG02056.hp2 HG03927.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0083a0001c0001t0001g0090 | 3 | HG01934.hp1 NA18962.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | NA18979.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(13): Show |
1 | a0004c0007t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0137a0003c0005t0001g0052others(1): Show | 4 | HG02074.hp1 HG02559.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0071a0003c0005t0003g0058 | 2 | HG02004.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0222 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0232a0003c0005t0001g0044 | 2 | HG02257.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(5): Show |
1 | a0001c0003t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0210a0004c0007t0001g0129 | 2 | HG01109.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATAT others(3): Show |
2 | a0001c0011t0001g0107a0003c0005t0001g0369 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATTT others(3): Show |
1 | a0004c0007t0001g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 241402880 | |||||
| chr2:241402880
|
A | T | 56 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0084others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.184-948A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402880 | ||||||
| chr2:241402881
|
T | TA | 4 | a0001c0001t0001g0298a0001c0001t0002g0373a0007c0013t0001g0028others(1): Show | 4 | HG02809.hp2 HG02965.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(1): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATA | 5 | a0001c0001t0001g0113a0001c0001t0001g0268a0001c0001t0001g0286others(2): Show | 5 | HG00558.hp2 HG02735.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATA | 5 | a0001c0001t0001g0131a0001c0001t0001g0142a0001c0003t0001g0053others(2): Show | 5 | HG01243.hp2 HG01928.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-947_184-946ins others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0285 | 3 | HG02074.hp2 HG03491.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.184-947_184-946ins others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(4): Show |
3 | a0001c0001t0001g0140a0001c0001t0001g0208a0001c0001t0002g0375 | 3 | HG00544.hp2 HG02572.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.184-947_184-946ins others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0302 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.184-947_184-946ins others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402881
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.184-947_184-946ins others(23): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402881 | ||||||
| chr2:241402882
|
T | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0109a0001c0001t0001g0118others(14): Show | 17 | HG00323.hp1 HG00558.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.184-946T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402882 | ||||||
| chr2:241402883
|
T | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0130others(10): Show | 13 | HG00558.hp2 HG01168.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.184-945T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402883 | ||||||
| chr2:241402884
|
T | A | 8 | a0001c0001t0001g0141a0001c0001t0001g0229a0001c0001t0001g0278others(5): Show | 8 | HG00323.hp1 HG02027.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-944T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402884 | ||||||
| chr2:241402885
|
T | A | 9 | a0001c0001t0001g0131a0001c0001t0001g0142a0001c0001t0001g0235others(6): Show | 9 | HG01928.hp1 HG02572.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-943T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402885 | ||||||
| chr2:241402886
|
T | A | 2 | a0001c0001t0001g0229a0001c0004t0001g0143 | 2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-942T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402886 | ||||||
| chr2:241402887
|
T | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0235a0001c0001t0001g0333others(1): Show | 4 | HG02965.hp2 HG03017.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-941T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402887 | ||||||
| chr2:241402888
|
T | A | 2 | a0001c0001t0001g0229a0001c0004t0001g0143 | 2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-940T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402888 | ||||||
| chr2:241402889
|
T | A | 2 | a0001c0001t0001g0142a0012c0023t0001g0203 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-939T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402889 | ||||||
| chr2:241402890
|
T | A | 2 | a0001c0001t0001g0229a0001c0004t0001g0143 | 2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-938T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402890 | ||||||
| chr2:241402891
|
T | A | 2 | a0001c0001t0001g0142a0012c0023t0001g0203 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-937T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402891 | ||||||
| chr2:241402892
|
T | A | 2 | a0001c0001t0001g0229a0001c0004t0001g0143 | 2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.184-936T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402892 | ||||||
| chr2:241402893
|
T | A | 2 | a0001c0001t0001g0142a0012c0023t0001g0203 | 2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.184-935T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402893 | ||||||
| chr2:241402895
|
T | A | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184-933T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402895 | ||||||
| chr2:241402911
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.184-917T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402911 | ||||||
| chr2:241402964
|
C | G | 26 | a0001c0001t0001g0268a0001c0001t0001g0304a0001c0001t0001g0305others(23): Show | 26 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.184-864C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241402964 | ||||||
| chr2:241403254
|
A | G | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.184-574A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403254 | ||||||
| chr2:241403353
|
T | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.184-475T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403353 | ||||||
| chr2:241403375
|
C | T | 2 | a0001c0006t0001g0246a0001c0006t0001g0251 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.184-453C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403375 | ||||||
| chr2:241403505
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.184-323C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403505 | ||||||
| chr2:241403543
|
C | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-285C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403543 | ||||||
| chr2:241403569
|
T | C | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.184-259T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 2/26 | chr2 | 241403569 | ||||||
| chr2:241403989
|
C | T | 29 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(26): Show | 29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.288+57C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241403989 | ||||||
| chr2:241404058
|
G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.288+126G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404058 | ||||||
| chr2:241404201
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.288+269C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404201 | ||||||
| chr2:241404289
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.288+357T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404289 | ||||||
| chr2:241404380
|
C | A | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.289-419C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404380 | ||||||
| chr2:241404388
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.289-411T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404388 | ||||||
| chr2:241404622
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.289-177G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404622 | ||||||
| chr2:241404670
|
G | C | 2 | a0003c0005t0001g0047a0003c0005t0001g0048 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.289-129G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404670 | ||||||
| chr2:241404713
|
T | C | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.289-86T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404713 | ||||||
| chr2:241404754
|
G | T | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289-45G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 3/26 | chr2 | 241404754 | ||||||
| chr2:241404918
|
A | G | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.331+77A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241404918 | ||||||
| chr2:241404969
|
C | T | 1 | a0001c0003t0001g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.331+128C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241404969 | ||||||
| chr2:241405078
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.331+237G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405078 | ||||||
| chr2:241405184
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.331+343T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405184 | ||||||
| chr2:241405261
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.331+420C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405261 | ||||||
| chr2:241405280
|
T | C | 4 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0004t0001g0171others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+439T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405280 | ||||||
| chr2:241405370
|
C | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.331+529C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405370 | ||||||
| chr2:241405371
|
G | A | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.331+530G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405371 | ||||||
| chr2:241405434
|
A | G | 5 | a0005c0008t0001g0147a0005c0008t0001g0150a0005c0008t0001g0152others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+593A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405434 | ||||||
| chr2:241405452
|
T | A | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+611T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405452 | ||||||
| chr2:241405507
|
A | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.331+666A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405507 | ||||||
| chr2:241405622
|
A | T | 1 | a0001c0001t0001g0284 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.331+781A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405622 | ||||||
| chr2:241405662
|
T | TG | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.331+825dupG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241405662 | |||||
| chr2:241405715
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.331+874C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405715 | ||||||
| chr2:241405725
|
G | A | 6 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0042others(3): Show | 6 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.331+884G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405725 | ||||||
| chr2:241405745
|
C | T | 1 | a0002c0002t0001g0258 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.331+904C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405745 | ||||||
| chr2:241405795
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.331+954G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405795 | ||||||
| chr2:241405802
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.331+961C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405802 | ||||||
| chr2:241405817
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.331+976T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405817 | ||||||
| chr2:241405865
|
C | T | 1 | a0002c0002t0001g0258 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.331+1024C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405865 | ||||||
| chr2:241405891
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.331+1050A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405891 | ||||||
| chr2:241405938
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.331+1097A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405938 | ||||||
| chr2:241405972
|
T | A | 2 | a0003c0005t0001g0195a0019c0027t0001g0145 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331+1131T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241405972 | ||||||
| chr2:241406086
|
A | C | 9 | a0001c0001t0001g0098a0001c0001t0002g0372a0001c0004t0001g0359others(6): Show | 9 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+1245A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406086 | ||||||
| chr2:241406099
|
C | T | 31 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.331+1258C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406099 | ||||||
| chr2:241406114
|
T | C | 3 | a0001c0001t0001g0329a0001c0004t0001g0168a0003c0005t0001g0194 | 3 | HG01934.hp2 HG02895.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.331+1273T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406114 | ||||||
| chr2:241406119
|
T | C | 42 | a0001c0001t0001g0066a0001c0001t0001g0105a0001c0001t0001g0205others(39): Show | 42 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.331+1278T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406119 | ||||||
| chr2:241406128
|
T | C | 5 | a0001c0004t0001g0178a0001c0004t0001g0180a0001c0004t0001g0181others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+1287T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406128 | ||||||
| chr2:241406132
|
C | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0115others(9): Show | 12 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+1291C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406132 | ||||||
| chr2:241406157
|
G | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0125others(14): Show | 17 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.331+1316G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406157 | ||||||
| chr2:241406179
|
G | A | 1 | a0002c0002t0001g0335 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.331+1338G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406179 | ||||||
| chr2:241406200
|
C | T | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.332-1337C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406200 | ||||||
| chr2:241406257
|
G | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-1280G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406257 | ||||||
| chr2:241406265
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.332-1272G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406265 | ||||||
| chr2:241406367
|
TTA | T | 10 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00639.hp2 HG01167.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1156_332-1155d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406367 | |||||
| chr2:241406411
|
G | GTA | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0188others(1): Show | 4 | HG00558.hp1 HG02083.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1117_332-1116d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406411 | |||||
| chr2:241406420
|
T | TAG | 13 | a0001c0001t0001g0094a0001c0001t0001g0103a0004c0007t0001g0096others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-1100_332-1099d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406420 | |||||
| chr2:241406420
|
TAG | T | 228 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(225): Show | 228 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.332-1100_332-1099d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 241406420 | |||||
| chr2:241406422
|
G | T | 86 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0003t0001g0007others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.332-1115G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406422 | ||||||
| chr2:241406424
|
G | T | 142 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(139): Show | 142 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.332-1113G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406424 | ||||||
| chr2:241406426
|
G | T | 73 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(70): Show | 73 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.332-1111G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406426 | ||||||
| chr2:241406628
|
G | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.332-909G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406628 | ||||||
| chr2:241406630
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.332-907G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406630 | ||||||
| chr2:241406642
|
C | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-895C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406642 | ||||||
| chr2:241406642
|
C | T | 26 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.332-895C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406642 | ||||||
| chr2:241406655
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.332-882G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406655 | ||||||
| chr2:241406831
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.332-706G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406831 | ||||||
| chr2:241406876
|
C | T | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.332-661C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406876 | ||||||
| chr2:241406941
|
G | C | 1 | a0001c0003t0001g0026 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.332-596G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406941 | ||||||
| chr2:241406965
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.332-572G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406965 | ||||||
| chr2:241406968
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.332-569C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406968 | ||||||
| chr2:241406991
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-546A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241406991 | ||||||
| chr2:241407001
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-536G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407001 | ||||||
| chr2:241407009
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0366a0001c0001t0001g0367 | 3 | HG01167.hp1 HG01169.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.332-528T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407009 | ||||||
| chr2:241407010
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.332-527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407010 | ||||||
| chr2:241407011
|
T | G | 17 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(14): Show | 17 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-526T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407011 | ||||||
| chr2:241407012
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-525G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | ||||||
| chr2:241407012
|
G | C | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.332-525G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | ||||||
| chr2:241407012
|
G | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | NA18981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.332-525G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407012 | ||||||
| chr2:241407015
|
G | A | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.332-522G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407015 | ||||||
| chr2:241407019
|
A | G | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.332-518A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407019 | ||||||
| chr2:241407056
|
C | G | 95 | a0001c0001t0001g0223a0001c0001t0001g0268a0001c0001t0001g0304others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.332-481C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407056 | ||||||
| chr2:241407090
|
G | C | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.332-447G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407090 | ||||||
| chr2:241407100
|
G | T | 1 | a0001c0001t0005g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.332-437G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407100 | ||||||
| chr2:241407104
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.332-433A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407104 | ||||||
| chr2:241407118
|
T | C | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.332-419T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 4/26 | chr2 | 241407118 | ||||||
| chr2:241407788
|
A | G | 2 | a0001c0001t0001g0071a0013c0024t0001g0087 | 2 | NA18970.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.410+173A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241407788 | ||||||
| chr2:241408049
|
G | T | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+434G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408049 | ||||||
| chr2:241408186
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.410+571A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408186 | ||||||
| chr2:241408199
|
C | T | 20 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(17): Show | 20 | HG00099.hp1 HG01123.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+584C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408199 | ||||||
| chr2:241408243
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.410+628G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408243 | ||||||
| chr2:241408307
|
G | A | 1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.410+692G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408307 | ||||||
| chr2:241408466
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.410+851C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408466 | ||||||
| chr2:241408492
|
G | A | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.410+877G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408492 | ||||||
| chr2:241408541
|
CA | C | 229 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.410+941delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241408541 | |||||
| chr2:241408541
|
CAA | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0083a0001c0001t0001g0201others(95): Show | 98 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.410+940_410+941del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241408541 | |||||
| chr2:241408556
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+941A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408556 | ||||||
| chr2:241408577
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.410+962C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408577 | ||||||
| chr2:241408667
|
C | T | 1 | a0004c0007t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.410+1052C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408667 | ||||||
| chr2:241408756
|
A | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.410+1141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408756 | ||||||
| chr2:241408835
|
G | A | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.410+1220G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408835 | ||||||
| chr2:241408858
|
T | C | 4 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+1243T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241408858 | ||||||
| chr2:241409004
|
A | G | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.410+1389A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409004 | ||||||
| chr2:241409038
|
T | TGATA | 146 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0064others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.410+1460_410+1463d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | |||||
| chr2:241409038
|
T | TGATAGAT others(1): Show |
82 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0086others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.410+1456_410+1463d others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | |||||
| chr2:241409038
|
T | TGATAGAT others(5): Show |
29 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.410+1452_410+1463d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | |||||
| chr2:241409038
|
T | TGATAGAT others(9): Show |
2 | a0001c0001t0001g0098a0003c0005t0001g0194 | 2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.410+1448_410+1463d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | |||||
| chr2:241409038
|
TGATA | T | 30 | a0001c0001t0001g0201a0001c0001t0001g0204a0001c0004t0001g0177others(27): Show | 30 | HG00597.hp1 HG01243.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.410+1460_410+1463d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409038 | |||||
| chr2:241409199
|
AT | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.410+1586delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241409199 | |||||
| chr2:241409245
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.410+1630T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409245 | ||||||
| chr2:241409416
|
G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.411-1617G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409416 | ||||||
| chr2:241409506
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.411-1527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409506 | ||||||
| chr2:241409831
|
T | C | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.411-1202T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409831 | ||||||
| chr2:241409846
|
A | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-1187A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409846 | ||||||
| chr2:241409852
|
C | T | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-1181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409852 | ||||||
| chr2:241409918
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.411-1115A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409918 | ||||||
| chr2:241409932
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.411-1101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241409932 | ||||||
| chr2:241410038
|
CAG | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | HG02965.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-994_411-993del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410038 | ||||||
| chr2:241410043
|
G | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0303 | 2 | NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.411-990G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410043 | ||||||
| chr2:241410182
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-851T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410182 | ||||||
| chr2:241410233
|
C | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.411-800C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410233 | ||||||
| chr2:241410237
|
C | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-796C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410237 | ||||||
| chr2:241410238
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.411-795C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410238 | ||||||
| chr2:241410388
|
A | G | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.411-645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410388 | ||||||
| chr2:241410433
|
C | CT | 260 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.411-586dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241410433 | |||||
| chr2:241410478
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.411-555A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410478 | ||||||
| chr2:241410479
|
T | C | 4 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(1): Show | 4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-554T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410479 | ||||||
| chr2:241410650
|
G | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.411-383G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410650 | ||||||
| chr2:241410677
|
G | GC | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG00423.hp1 HG02056.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.411-352dupC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 241410677 | |||||
| chr2:241410743
|
T | A | 6 | a0001c0003t0001g0007a0001c0003t0001g0022a0001c0003t0001g0023others(3): Show | 6 | NA18949.hp2 NA18951.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-290T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410743 | ||||||
| chr2:241410892
|
G | A | 1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.411-141G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410892 | ||||||
| chr2:241410938
|
A | C | 4 | a0001c0004t0001g0161a0001c0004t0001g0162a0001c0004t0001g0163others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-95A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410938 | ||||||
| chr2:241410974
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-59A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 5/26 | chr2 | 241410974 | ||||||
| chr2:241411190
|
T | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+60T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411190 | ||||||
| chr2:241411215
|
T | G | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.508+85T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411215 | ||||||
| chr2:241411367
|
G | A | 2 | a0001c0006t0001g0246a0001c0006t0001g0251 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.508+237G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411367 | ||||||
| chr2:241411506
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.508+376C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411506 | ||||||
| chr2:241411522
|
A | G | 373 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(370): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.508+392A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411522 | ||||||
| chr2:241411529
|
A | G | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.508+399A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411529 | ||||||
| chr2:241411571
|
C | T | 1 | a0001c0003t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.508+441C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411571 | ||||||
| chr2:241411595
|
A | G | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.508+465A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411595 | ||||||
| chr2:241411651
|
A | G | 291 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.508+521A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411651 | ||||||
| chr2:241411740
|
C | G | 1 | a0005c0008t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508+610C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411740 | ||||||
| chr2:241411816
|
G | A | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.508+686G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411816 | ||||||
| chr2:241411860
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508+730A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411860 | ||||||
| chr2:241411964
|
T | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.508+834T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411964 | ||||||
| chr2:241411970
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.508+840G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241411970 | ||||||
| chr2:241412065
|
C | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.508+935C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412065 | ||||||
| chr2:241412224
|
C | G | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.509-1083C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412224 | ||||||
| chr2:241412264
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.509-1043C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412264 | ||||||
| chr2:241412398
|
A | G | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.509-909A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412398 | ||||||
| chr2:241412471
|
A | C | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.509-836A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412471 | ||||||
| chr2:241412630
|
C | G | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.509-677C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412630 | ||||||
| chr2:241412642
|
A | T | 1 | a0005c0008t0001g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-665A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412642 | ||||||
| chr2:241412693
|
A | G | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.509-614A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412693 | ||||||
| chr2:241412760
|
C | T | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-547C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412760 | ||||||
| chr2:241412831
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.509-476C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412831 | ||||||
| chr2:241412842
|
A | G | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.509-465A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241412842 | ||||||
| chr2:241413166
|
T | C | 2 | a0003c0005t0001g0046a0003c0005t0001g0049 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509-141T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413166 | ||||||
| chr2:241413167
|
A | T | 85 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(82): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.509-140A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413167 | ||||||
| chr2:241413218
|
A | AT | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.509-80dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr2 | 241413218 | |||||
| chr2:241413218
|
A | T | 2 | a0001c0001t0001g0113a0010c0026t0001g0116 | 2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.509-89A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 6/26 | chr2 | 241413218 | ||||||
| chr2:241413762
|
G | C | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+341G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413762 | ||||||
| chr2:241413867
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.623+446A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413867 | ||||||
| chr2:241413936
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.623+515G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241413936 | ||||||
| chr2:241413940
|
C | CA | 6 | a0001c0001t0001g0088a0001c0001t0002g0372a0001c0001t0002g0373others(3): Show | 6 | HG01261.hp2 HG02523.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+534dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241413940 | |||||
| chr2:241413940
|
CA | C | 11 | a0001c0001t0001g0268a0001c0003t0001g0035a0003c0005t0001g0047others(8): Show | 11 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.623+534delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241413940 | |||||
| chr2:241414078
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.623+657G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414078 | ||||||
| chr2:241414289
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.623+868G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414289 | ||||||
| chr2:241414409
|
G | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+988G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414409 | ||||||
| chr2:241414438
|
T | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.623+1017T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414438 | ||||||
| chr2:241414525
|
A | G | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.623+1104A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414525 | ||||||
| chr2:241414606
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.623+1185C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414606 | ||||||
| chr2:241414608
|
G | A | 1 | a0003c0005t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+1187G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414608 | ||||||
| chr2:241414715
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.623+1294A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414715 | ||||||
| chr2:241414725
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.623+1304G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414725 | ||||||
| chr2:241414752
|
G | A | 6 | a0001c0001t0001g0271a0001c0001t0002g0372a0001c0001t0002g0373others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.623+1331G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414752 | ||||||
| chr2:241414956
|
A | G | 22 | a0001c0003t0001g0062a0002c0002t0001g0200a0002c0002t0001g0338others(19): Show | 22 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.623+1535A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241414956 | ||||||
| chr2:241415088
|
C | T | 1 | a0001c0003t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.623+1667C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415088 | ||||||
| chr2:241415181
|
G | C | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.623+1760G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415181 | ||||||
| chr2:241415217
|
T | C | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.623+1796T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415217 | ||||||
| chr2:241415232
|
A | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.623+1811A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415232 | ||||||
| chr2:241415235
|
C | T | 1 | a0009c0012t0001g0002 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.623+1814C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415235 | ||||||
| chr2:241415413
|
A | G | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.623+1992A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415413 | ||||||
| chr2:241415431
|
C | G | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.623+2010C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415431 | ||||||
| chr2:241415463
|
A | C | 1 | a0003c0005t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.623+2042A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415463 | ||||||
| chr2:241415564
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0231a0001c0001t0001g0232others(80): Show | 83 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.623+2143C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415564 | ||||||
| chr2:241415576
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.623+2155G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415576 | ||||||
| chr2:241415779
|
T | A | 1 | a0003c0005t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624-2183T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415779 | ||||||
| chr2:241415885
|
A | C | 1 | a0003c0005t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.624-2077A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415885 | ||||||
| chr2:241415987
|
T | TTC | 22 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0003t0001g0007others(19): Show | 22 | HG00621.hp2 HG00639.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1973_624-1972d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415987 | |||||
| chr2:241415989
|
C | CTCTCTG | 4 | a0001c0001t0001g0366a0001c0001t0001g0367a0009c0012t0001g0001others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTCTG | 18 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0220others(15): Show | 18 | HG00609.hp1 HG01106.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTCTGTG | 18 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0210others(15): Show | 18 | HG00423.hp2 HG00544.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.624-1972_624-1971i others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTCTGTGT others(3): Show |
1 | a0001c0001t0001g0212 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.624-1972_624-1971i others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTG | 50 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0063others(47): Show | 50 | HG00323.hp2 HG00423.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.624-1929_624-1928d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTGTG | 22 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0094others(19): Show | 22 | HG00280.hp2 HG00544.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1931_624-1928d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTGTGTG | 25 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0119others(22): Show | 25 | HG00558.hp1 HG01099.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.624-1933_624-1928d others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTGTGTGT others(1): Show |
6 | a0003c0005t0001g0046a0003c0005t0001g0052a0003c0005t0001g0059others(3): Show | 6 | HG01496.hp2 HG01934.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.624-1935_624-1928d others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTGTGTGT others(3): Show |
6 | a0003c0005t0001g0040a0003c0005t0001g0043a0003c0005t0001g0047others(3): Show | 6 | HG00099.hp1 HG02004.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-1937_624-1928d others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
C | CTGTGTGT others(5): Show |
1 | a0003c0005t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.624-1939_624-1928d others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTG | C | 19 | a0001c0001t0001g0067a0001c0001t0001g0081a0001c0001t0001g0092others(16): Show | 19 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.624-1929_624-1928d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTGTG | C | 53 | a0001c0001t0001g0136a0001c0001t0001g0201a0001c0001t0001g0202others(50): Show | 53 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.624-1931_624-1928d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTGTGTG | C | 22 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0262others(19): Show | 22 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.624-1933_624-1928d others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0378a0005c0008t0001g0146 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.624-1941_624-1928d others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTGTGTGT others(13): Show |
C | 35 | a0001c0001t0001g0158a0001c0001t0001g0310a0001c0001t0001g0312others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.624-1947_624-1928d others(22): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415989
|
CTGTGTGT others(15): Show |
C | 4 | a0001c0001t0001g0268a0001c0001t0001g0322a0001c0001t0001g0326others(1): Show | 4 | HG02083.hp1 NA18747.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1949_624-1928d others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241415989 | |||||
| chr2:241415991
|
G | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0239others(55): Show | 58 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.624-1971G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415991 | ||||||
| chr2:241415993
|
G | C | 52 | a0001c0001t0001g0206a0001c0001t0001g0234a0001c0001t0001g0238others(49): Show | 52 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.624-1969G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415993 | ||||||
| chr2:241415994
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.624-1968T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415994 | ||||||
| chr2:241415995
|
G | C | 77 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(74): Show | 77 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.624-1967G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415995 | ||||||
| chr2:241415997
|
G | C | 24 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0262others(21): Show | 24 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.624-1965G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415997 | ||||||
| chr2:241415999
|
G | C | 8 | a0001c0001t0001g0264a0001c0004t0001g0359a0001c0004t0001g0360others(5): Show | 8 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.624-1963G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241415999 | ||||||
| chr2:241416001
|
G | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-1961G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416001 | ||||||
| chr2:241416005
|
G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-1957G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416005 | ||||||
| chr2:241416007
|
G | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-1955G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416007 | ||||||
| chr2:241416011
|
G | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(1): Show | 4 | HG02132.hp1 HG02135.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1951G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416011 | ||||||
| chr2:241416013
|
G | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0322a0001c0001t0001g0326others(1): Show | 4 | HG02083.hp1 NA18747.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.624-1949G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416013 | ||||||
| chr2:241416119
|
CTG | C | 112 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(109): Show | 112 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.624-1836_624-1835d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241416119 | |||||
| chr2:241416137
|
T | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-1825T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416137 | ||||||
| chr2:241416254
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.624-1708G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416254 | ||||||
| chr2:241416283
|
A | G | 1 | a0018c0016t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.624-1679A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416283 | ||||||
| chr2:241416286
|
G | A | 30 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.624-1676G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416286 | ||||||
| chr2:241416314
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.624-1648A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416314 | ||||||
| chr2:241416321
|
T | C | 1 | a0003c0005t0001g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.624-1641T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416321 | ||||||
| chr2:241416343
|
C | T | 1 | a0001c0001t0009g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.624-1619C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416343 | ||||||
| chr2:241416400
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0131others(2): Show | 5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.624-1562T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416400 | ||||||
| chr2:241416432
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.624-1530A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416432 | ||||||
| chr2:241416680
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.624-1282A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416680 | ||||||
| chr2:241416710
|
G | A | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.624-1252G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416710 | ||||||
| chr2:241416779
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.624-1183C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416779 | ||||||
| chr2:241416824
|
G | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.624-1138G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241416824 | ||||||
| chr2:241417022
|
C | T | 2 | a0001c0004t0001g0370a0005c0008t0001g0150 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.624-940C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417022 | ||||||
| chr2:241417025
|
G | A | 4 | a0001c0003t0001g0034a0001c0003t0001g0035a0001c0003t0001g0037others(1): Show | 4 | NA18972.hp1 NA18986.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.624-937G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417025 | ||||||
| chr2:241417076
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.624-886G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417076 | ||||||
| chr2:241417085
|
G | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.624-877G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417085 | ||||||
| chr2:241417240
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.624-722G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417240 | ||||||
| chr2:241417309
|
G | A | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-653G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417309 | ||||||
| chr2:241417310
|
A | G | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-652A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417310 | ||||||
| chr2:241417360
|
T | C | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-602T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417360 | ||||||
| chr2:241417361
|
C | T | 1 | a0001c0003t0001g0035 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.624-601C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417361 | ||||||
| chr2:241417414
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.624-548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417414 | ||||||
| chr2:241417472
|
G | A | 63 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.624-490G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417472 | ||||||
| chr2:241417479
|
C | T | 17 | a0001c0004t0001g0165a0001c0004t0001g0166a0001c0004t0001g0167others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.624-483C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417479 | ||||||
| chr2:241417588
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.624-374G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417588 | ||||||
| chr2:241417642
|
A | AT | 276 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.624-318dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr2 | 241417642 | |||||
| chr2:241417694
|
G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.624-268G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417694 | ||||||
| chr2:241417900
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.624-62C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 7/26 | chr2 | 241417900 | ||||||
| chr2:241418188
|
T | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+79T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418188 | ||||||
| chr2:241418268
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.771+159C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418268 | ||||||
| chr2:241418393
|
C | G | 4 | a0001c0004t0001g0362a0001c0010t0001g0363a0001c0010t0001g0364others(1): Show | 4 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+284C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418393 | ||||||
| chr2:241418494
|
GTC | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.771+389_771+390del others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241418494 | |||||
| chr2:241418537
|
T | C | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.771+428T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418537 | ||||||
| chr2:241418857
|
C | T | 5 | a0001c0004t0001g0361a0001c0004t0001g0362a0001c0010t0001g0363others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+748C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418857 | ||||||
| chr2:241418865
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.771+756A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418865 | ||||||
| chr2:241418884
|
G | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.771+775G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241418884 | ||||||
| chr2:241419001
|
A | G | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+892A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419001 | ||||||
| chr2:241419069
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+960A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419069 | ||||||
| chr2:241419204
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.771+1095G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419204 | ||||||
| chr2:241419525
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+1416G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419525 | ||||||
| chr2:241419544
|
A | T | 1 | a0001c0004t0001g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.771+1435A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419544 | ||||||
| chr2:241419662
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+1553A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419662 | ||||||
| chr2:241419820
|
T | A | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.771+1711T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419820 | ||||||
| chr2:241419925
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.771+1816A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241419925 | ||||||
| chr2:241420168
|
T | C | 1 | a0002c0002t0001g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.771+2059T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420168 | ||||||
| chr2:241420237
|
A | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+2128A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420237 | ||||||
| chr2:241420244
|
C | G | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.771+2135C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420244 | ||||||
| chr2:241420404
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2295G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420404 | ||||||
| chr2:241420490
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.771+2381G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420490 | ||||||
| chr2:241420605
|
C | T | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.771+2496C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420605 | ||||||
| chr2:241420670
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0004g0265 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.771+2561A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420670 | ||||||
| chr2:241420686
|
A | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.771+2577A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420686 | ||||||
| chr2:241420830
|
T | G | 287 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0158others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.771+2721T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420830 | ||||||
| chr2:241420895
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.771+2786G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420895 | ||||||
| chr2:241420919
|
C | T | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.771+2810C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241420919 | ||||||
| chr2:241421203
|
A | G | 5 | a0001c0004t0001g0361a0001c0004t0001g0362a0001c0010t0001g0363others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+3094A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421203 | ||||||
| chr2:241421281
|
G | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3172G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421281 | ||||||
| chr2:241421307
|
C | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3198C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421307 | ||||||
| chr2:241421309
|
C | G | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.771+3200C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421309 | ||||||
| chr2:241421504
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.771+3395G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421504 | ||||||
| chr2:241421552
|
G | A | 1 | a0001c0001t0002g0375 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.771+3443G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421552 | ||||||
| chr2:241421718
|
GAT | G | 273 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.771+3613_771+3614d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241421718 | |||||
| chr2:241421721
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.771+3612A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421721 | ||||||
| chr2:241421834
|
G | A | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771+3725G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421834 | ||||||
| chr2:241421883
|
C | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.771+3774C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421883 | ||||||
| chr2:241421915
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+3806G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241421915 | ||||||
| chr2:241422048
|
A | G | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+3939A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422048 | ||||||
| chr2:241422131
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.771+4022C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422131 | ||||||
| chr2:241422153
|
C | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+4044C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422153 | ||||||
| chr2:241422182
|
G | A | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.771+4073G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422182 | ||||||
| chr2:241422200
|
A | G | 286 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.771+4091A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422200 | ||||||
| chr2:241422260
|
C | CA | 11 | a0001c0001t0001g0121a0001c0004t0001g0174a0001c0004t0001g0370others(8): Show | 11 | HG00323.hp1 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.771+4171dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | |||||
| chr2:241422260
|
CA | C | 71 | a0001c0001t0001g0094a0001c0001t0001g0205a0001c0001t0001g0206others(68): Show | 71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.771+4171delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | |||||
| chr2:241422260
|
CAA | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0204others(61): Show | 64 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.771+4170_771+4171d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422260 | |||||
| chr2:241422312
|
A | G | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.771+4203A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422312 | ||||||
| chr2:241422402
|
C | CA | 45 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(42): Show | 45 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.771+4304dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241422402 | |||||
| chr2:241422413
|
A | C | 3 | a0001c0001t0009g0104a0001c0011t0001g0107a0001c0011t0001g0108 | 3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.771+4304A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422413 | ||||||
| chr2:241422474
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.771+4365C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422474 | ||||||
| chr2:241422594
|
G | A | 1 | a0003c0005t0001g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.771+4485G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422594 | ||||||
| chr2:241422753
|
C | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.771+4644C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422753 | ||||||
| chr2:241422825
|
A | G | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.771+4716A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422825 | ||||||
| chr2:241422846
|
C | A | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.771+4737C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422846 | ||||||
| chr2:241422894
|
T | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.771+4785T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241422894 | ||||||
| chr2:241423261
|
C | T | 1 | a0001c0003t0001g0025 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.771+5152C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423261 | ||||||
| chr2:241423296
|
G | A | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.771+5187G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423296 | ||||||
| chr2:241423605
|
A | G | 1 | a0001c0004t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.771+5496A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423605 | ||||||
| chr2:241423649
|
T | G | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.771+5540T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423649 | ||||||
| chr2:241423724
|
C | T | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.771+5615C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423724 | ||||||
| chr2:241423733
|
A | G | 5 | a0005c0008t0001g0144a0005c0008t0001g0148a0005c0008t0001g0154others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+5624A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423733 | ||||||
| chr2:241423911
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.771+5802T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423911 | ||||||
| chr2:241423934
|
A | G | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.771+5825A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241423934 | ||||||
| chr2:241424140
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.771+6031C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424140 | ||||||
| chr2:241424149
|
A | C | 286 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.771+6040A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424149 | ||||||
| chr2:241424196
|
G | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(83): Show | 86 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.771+6087G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424196 | ||||||
| chr2:241424527
|
A | G | 1 | a0018c0016t0001g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.771+6418A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424527 | ||||||
| chr2:241424692
|
AAT | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.771+6585_771+6586d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241424692 | |||||
| chr2:241424704
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.771+6595G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424704 | ||||||
| chr2:241424754
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.771+6645A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424754 | ||||||
| chr2:241424763
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.771+6654G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424763 | ||||||
| chr2:241424783
|
C | T | 1 | a0011c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.771+6674C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424783 | ||||||
| chr2:241424814
|
T | G | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.771+6705T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424814 | ||||||
| chr2:241424880
|
T | C | 286 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.771+6771T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241424880 | ||||||
| chr2:241425122
|
G | A | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.772-6557G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425122 | ||||||
| chr2:241425122
|
G | T | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.772-6557G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425122 | ||||||
| chr2:241425286
|
C | T | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.772-6393C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425286 | ||||||
| chr2:241425465
|
G | A | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-6214G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425465 | ||||||
| chr2:241425498
|
T | C | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.772-6181T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425498 | ||||||
| chr2:241425634
|
T | TA | 58 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0081others(55): Show | 58 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.772-6017dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | |||||
| chr2:241425634
|
T | TAA | 10 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0024others(7): Show | 10 | HG00280.hp1 HG00642.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-6018_772-6017d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | |||||
| chr2:241425634
|
TA | T | 77 | a0001c0001t0001g0064a0001c0001t0001g0085a0001c0001t0001g0119others(74): Show | 77 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.772-6017delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | |||||
| chr2:241425634
|
TAA | T | 12 | a0001c0004t0001g0370a0001c0006t0001g0236a0001c0006t0001g0240others(9): Show | 12 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.772-6018_772-6017d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425634 | |||||
| chr2:241425688
|
A | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772-5991A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425688 | ||||||
| chr2:241425713
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.772-5966G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425713 | ||||||
| chr2:241425741
|
CT | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0112a0001c0001t0001g0142others(208): Show | 211 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.772-5918delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425741 | |||||
| chr2:241425741
|
CTT | C | 76 | a0001c0001t0001g0158a0001c0001t0001g0206a0001c0001t0001g0333others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.772-5919_772-5918d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425741 | |||||
| chr2:241425764
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0131others(2): Show | 5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-5915G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425764 | ||||||
| chr2:241425863
|
G | GT | 46 | a0001c0001t0001g0068a0001c0001t0001g0205a0001c0001t0001g0206others(43): Show | 46 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.772-5803dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425863 | |||||
| chr2:241425863
|
GT | G | 6 | a0001c0001t0001g0269a0001c0003t0001g0053a0001c0004t0001g0175others(3): Show | 6 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-5803delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425863 | |||||
| chr2:241425864
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.772-5815T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425864 | ||||||
| chr2:241425937
|
TA | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-5739delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241425937 | |||||
| chr2:241425938
|
A | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-5741A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241425938 | ||||||
| chr2:241426228
|
C | T | 2 | a0001c0001t0001g0158a0001c0004t0001g0157 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.772-5451C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426228 | ||||||
| chr2:241426520
|
G | A | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.772-5159G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426520 | ||||||
| chr2:241426538
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-5141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426538 | ||||||
| chr2:241426622
|
G | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.772-5057G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426622 | ||||||
| chr2:241426640
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-5039G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426640 | ||||||
| chr2:241426645
|
G | A | 1 | a0014c0018t0001g0339 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.772-5034G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426645 | ||||||
| chr2:241426847
|
C | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.772-4832C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426847 | ||||||
| chr2:241426853
|
A | G | 1 | a0002c0002t0001g0343 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.772-4826A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426853 | ||||||
| chr2:241426960
|
C | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0201others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.772-4719C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426960 | ||||||
| chr2:241426962
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-4717C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241426962 | ||||||
| chr2:241427085
|
A | G | 34 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(31): Show | 34 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.772-4594A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427085 | ||||||
| chr2:241427189
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.772-4490C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427189 | ||||||
| chr2:241427238
|
A | AAC | 29 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(26): Show | 29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.772-4427_772-4426d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241427238 | |||||
| chr2:241427384
|
C | T | 2 | a0002c0002t0001g0200a0002c0002t0001g0358 | 2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.772-4295C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427384 | ||||||
| chr2:241427449
|
G | A | 1 | a0001c0004t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.772-4230G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427449 | ||||||
| chr2:241427693
|
T | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.772-3986T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427693 | ||||||
| chr2:241427714
|
T | A | 11 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(8): Show | 11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-3965T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427714 | ||||||
| chr2:241427765
|
G | A | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.772-3914G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427765 | ||||||
| chr2:241427829
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.772-3850G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427829 | ||||||
| chr2:241427955
|
G | A | 4 | a0001c0001t0001g0378a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG02258.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.772-3724G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427955 | ||||||
| chr2:241427956
|
C | T | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.772-3723C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427956 | ||||||
| chr2:241427967
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.772-3712T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427967 | ||||||
| chr2:241427987
|
C | T | 341 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.772-3692C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241427987 | ||||||
| chr2:241428001
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772-3678C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428001 | ||||||
| chr2:241428009
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3670G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428009 | ||||||
| chr2:241428011
|
C | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3668C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428011 | ||||||
| chr2:241428040
|
A | C | 2 | a0006c0009t0001g0183a0006c0009t0001g0184 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.772-3639A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428040 | ||||||
| chr2:241428045
|
C | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-3634C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428045 | ||||||
| chr2:241428046
|
A | C | 26 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.772-3633A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428046 | ||||||
| chr2:241428046
|
A | G | 10 | a0001c0001t0001g0311a0001c0004t0001g0359a0001c0004t0001g0360others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-3633A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428046 | ||||||
| chr2:241428056
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3623A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428056 | ||||||
| chr2:241428058
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3621G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428058 | ||||||
| chr2:241428062
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-3617A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428062 | ||||||
| chr2:241428074
|
C | T | 29 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.772-3605C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428074 | ||||||
| chr2:241428202
|
G | T | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.772-3477G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428202 | ||||||
| chr2:241428217
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.772-3462A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428217 | ||||||
| chr2:241428234
|
C | CT | 226 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0158others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.772-3427dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428234 | |||||
| chr2:241428234
|
C | CTT | 11 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0238others(8): Show | 11 | HG00639.hp1 HG01358.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-3428_772-3427d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428234 | |||||
| chr2:241428261
|
G | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-3418G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428261 | ||||||
| chr2:241428282
|
T | C | 8 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0262others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-3397T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428282 | ||||||
| chr2:241428294
|
G | A | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.772-3385G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428294 | ||||||
| chr2:241428298
|
AG | A | 5 | a0006c0009t0001g0183a0006c0009t0001g0184a0006c0009t0001g0185others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-3380delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428298 | ||||||
| chr2:241428401
|
AT | A | 35 | a0001c0001t0001g0084a0001c0001t0001g0205a0001c0001t0001g0206others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.772-3263delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428401 | |||||
| chr2:241428440
|
C | T | 2 | a0003c0005t0001g0198a0003c0005t0001g0199 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.772-3239C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428440 | ||||||
| chr2:241428451
|
C | T | 1 | a0011c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.772-3228C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428451 | ||||||
| chr2:241428461
|
G | A | 1 | a0001c0011t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.772-3218G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428461 | ||||||
| chr2:241428498
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(2): Show | 5 | NA18953.hp1 NA19000.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-3181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428498 | ||||||
| chr2:241428500
|
A | G | 29 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(26): Show | 29 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.772-3179A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428500 | ||||||
| chr2:241428536
|
G | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-3143G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428536 | ||||||
| chr2:241428590
|
GT | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-3086delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428590 | |||||
| chr2:241428625
|
AT | A | 7 | a0001c0001t0001g0142a0001c0001t0001g0378a0001c0004t0001g0143others(4): Show | 7 | HG00408.hp1 HG01358.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.772-3041delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241428625 | |||||
| chr2:241428655
|
G | A | 284 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.772-3024G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428655 | ||||||
| chr2:241428675
|
T | C | 2 | a0001c0003t0001g0060a0001c0003t0008g0061 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.772-3004T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428675 | ||||||
| chr2:241428689
|
A | G | 11 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(8): Show | 11 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.772-2990A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428689 | ||||||
| chr2:241428726
|
C | T | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-2953C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428726 | ||||||
| chr2:241428800
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.772-2879G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428800 | ||||||
| chr2:241428910
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-2769C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428910 | ||||||
| chr2:241428993
|
G | A | 6 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0042others(3): Show | 6 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-2686G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241428993 | ||||||
| chr2:241429278
|
A | G | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.772-2401A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429278 | ||||||
| chr2:241429310
|
G | A | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-2369G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429310 | ||||||
| chr2:241429352
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.772-2327C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429352 | ||||||
| chr2:241429443
|
G | T | 1 | a0003c0005t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.772-2236G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429443 | ||||||
| chr2:241429632
|
A | G | 32 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(29): Show | 32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.772-2047A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429632 | ||||||
| chr2:241429656
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-2023G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429656 | ||||||
| chr2:241429709
|
C | A | 6 | a0001c0003t0001g0027a0001c0003t0001g0034a0001c0003t0001g0035others(3): Show | 6 | HG02132.hp2 NA18972.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-1970C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429709 | ||||||
| chr2:241429868
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-1811A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241429868 | ||||||
| chr2:241430270
|
A | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.772-1409A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430270 | ||||||
| chr2:241430450
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.772-1229C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430450 | ||||||
| chr2:241430482
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.772-1197A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430482 | ||||||
| chr2:241430733
|
A | C | 3 | a0001c0001t0001g0378a0009c0012t0001g0001a0009c0012t0001g0002 | 3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.772-946A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430733 | ||||||
| chr2:241430868
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.772-811C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430868 | ||||||
| chr2:241430952
|
A | T | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.772-727A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430952 | ||||||
| chr2:241430999
|
C | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.772-680C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241430999 | ||||||
| chr2:241431004
|
A | G | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-675A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431004 | ||||||
| chr2:241431083
|
A | T | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.772-596A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431083 | ||||||
| chr2:241431148
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0330a0001c0001t0001g0331 | 3 | NA18943.hp2 NA19012.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.772-531A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431148 | ||||||
| chr2:241431158
|
A | T | 1 | a0003c0005t0001g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.772-521A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431158 | ||||||
| chr2:241431196
|
G | C | 1 | a0003c0005t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.772-483G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431196 | ||||||
| chr2:241431248
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.772-431A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431248 | ||||||
| chr2:241431303
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.772-376C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431303 | ||||||
| chr2:241431336
|
G | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(173): Show | 176 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.772-343G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431336 | ||||||
| chr2:241431372
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00733.hp1 HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.772-307G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431372 | ||||||
| chr2:241431429
|
TG | T | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.772-248delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 241431429 | |||||
| chr2:241431540
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.772-139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 8/26 | chr2 | 241431540 | ||||||
| chr2:241431810
|
T | TTTTA | 3 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0003t0001g0053 | 3 | HG01167.hp1 HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.867+56_867+59dupAT others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241431810 | |||||
| chr2:241431826
|
A | T | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+52A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431826 | ||||||
| chr2:241431830
|
A | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0272a0001c0001t0001g0304others(20): Show | 23 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+56A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431830 | ||||||
| chr2:241431842
|
C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.867+68C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431842 | ||||||
| chr2:241431923
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.867+149G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241431923 | ||||||
| chr2:241432053
|
T | C | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.867+279T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432053 | ||||||
| chr2:241432282
|
G | C | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.867+508G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432282 | ||||||
| chr2:241432410
|
G | A | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.867+636G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432410 | ||||||
| chr2:241432596
|
G | A | 1 | a0001c0003t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.867+822G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432596 | ||||||
| chr2:241432688
|
A | T | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+914A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432688 | ||||||
| chr2:241432689
|
T | G | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+915T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432689 | ||||||
| chr2:241432691
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.867+917G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432691 | ||||||
| chr2:241432880
|
A | T | 5 | a0005c0008t0001g0144a0005c0008t0001g0148a0005c0008t0001g0154others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+1106A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432880 | ||||||
| chr2:241432953
|
A | G | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.867+1179A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241432953 | ||||||
| chr2:241433011
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.868-1147G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433011 | ||||||
| chr2:241433059
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.868-1099A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433059 | ||||||
| chr2:241433095
|
C | T | 5 | a0005c0008t0001g0146a0005c0008t0001g0147a0005c0008t0001g0150others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-1063C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433095 | ||||||
| chr2:241433104
|
A | G | 3 | a0001c0004t0001g0161a0001c0004t0001g0162a0001c0004t0001g0163 | 3 | HG01884.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.868-1054A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433104 | ||||||
| chr2:241433129
|
T | TA | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.868-1016dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241433129 | |||||
| chr2:241433155
|
T | A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.868-1003T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433155 | ||||||
| chr2:241433160
|
G | A | 1 | a0002c0002t0001g0348 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.868-998G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433160 | ||||||
| chr2:241433316
|
T | C | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.868-842T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241433316 | ||||||
| chr2:241433503
|
TATACC | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.868-652_868-648del others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 241433503 | |||||
| chr2:241434090
|
C | T | 1 | a0001c0001t0001g0368 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.868-68C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434090 | ||||||
| chr2:241434096
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.868-62T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434096 | ||||||
| chr2:241434145
|
G | A | 1 | a0010c0026t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.868-13G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 9/26 | chr2 | 241434145 | ||||||
| chr2:241434335
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1031+14C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434335 | ||||||
| chr2:241434566
|
T | A | 1 | a0001c0001t0001g0318 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1031+245T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434566 | ||||||
| chr2:241434744
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1032-218C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434744 | ||||||
| chr2:241434763
|
A | C | 1 | a0001c0001t0001g0307 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1032-199A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434763 | ||||||
| chr2:241434792
|
C | T | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1032-170C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434792 | ||||||
| chr2:241434800
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1032-162C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434800 | ||||||
| chr2:241434823
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1032-139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434823 | ||||||
| chr2:241434833
|
C | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1032-129C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434833 | ||||||
| chr2:241434918
|
C | G | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1032-44C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434918 | ||||||
| chr2:241434943
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1032-19T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 10/26 | chr2 | 241434943 | ||||||
| chr2:241435038
|
C | T | 2 | a0003c0005t0001g0046a0003c0005t0001g0049 | 2 | HG02055.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1100+8C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435038 | ||||||
| chr2:241435104
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1100+74C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435104 | ||||||
| chr2:241435130
|
G | A | 1 | a0019c0027t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1100+100G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435130 | ||||||
| chr2:241435162
|
C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1100+132C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435162 | ||||||
| chr2:241435198
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1100+168A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435198 | ||||||
| chr2:241435218
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1100+188C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435218 | ||||||
| chr2:241435243
|
A | G | 1 | a0005c0014t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1100+213A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435243 | ||||||
| chr2:241435261
|
G | GT | 10 | a0002c0002t0001g0344a0002c0002t0001g0345a0002c0002t0001g0346others(7): Show | 10 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+239dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435261 | |||||
| chr2:241435270
|
G | GT | 16 | a0001c0001t0001g0084a0001c0001t0001g0206a0001c0001t0001g0219others(13): Show | 16 | HG00642.hp1 HG02056.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1100+254dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435270 | |||||
| chr2:241435294
|
C | T | 2 | a0003c0005t0001g0046a0003c0005t0001g0049 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1100+264C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435294 | ||||||
| chr2:241435342
|
G | GT | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1100+313dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435342 | |||||
| chr2:241435376
|
G | A | 1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1100+346G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435376 | ||||||
| chr2:241435452
|
A | G | 3 | a0001c0001t0009g0104a0001c0011t0001g0107a0001c0011t0001g0108 | 3 | HG02818.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1100+422A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435452 | ||||||
| chr2:241435510
|
A | AT | 100 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0201others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1100+499dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435510 | |||||
| chr2:241435593
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1100+563G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435593 | ||||||
| chr2:241435598
|
G | A | 33 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(30): Show | 33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1100+568G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435598 | ||||||
| chr2:241435757
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1101-724C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435757 | ||||||
| chr2:241435758
|
G | A | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1101-723G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435758 | ||||||
| chr2:241435833
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1101-648T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241435833 | ||||||
| chr2:241435908
|
A | AT | 87 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0201others(84): Show | 87 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1101-551dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | |||||
| chr2:241435908
|
A | ATT | 8 | a0001c0001t0001g0270a0001c0001t0001g0288a0001c0001t0001g0294others(5): Show | 8 | HG02135.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1101-552_1101-551d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | |||||
| chr2:241435908
|
AT | A | 76 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0112others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1101-551delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 241435908 | |||||
| chr2:241436014
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1101-467G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436014 | ||||||
| chr2:241436248
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1101-233C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436248 | ||||||
| chr2:241436398
|
A | T | 30 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(27): Show | 30 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1101-83A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 11/26 | chr2 | 241436398 | ||||||
| chr2:241436637
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158+99A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436637 | ||||||
| chr2:241436771
|
G | T | 39 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(36): Show | 39 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1158+233G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436771 | ||||||
| chr2:241436861
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1158+323G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436861 | ||||||
| chr2:241436918
|
T | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1158+380T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436918 | ||||||
| chr2:241436987
|
A | G | 4 | a0002c0002t0001g0254a0002c0002t0001g0260a0002c0002t0001g0261others(1): Show | 4 | HG00639.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158+449A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241436987 | ||||||
| chr2:241437084
|
TACTA | T | 44 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1158+551_1158+554d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437084 | |||||
| chr2:241437092
|
A | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1158+554A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437092 | ||||||
| chr2:241437190
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1158+652T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437190 | ||||||
| chr2:241437259
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1158+721A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437259 | ||||||
| chr2:241437260
|
C | G | 1 | a0005c0008t0001g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1158+722C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437260 | ||||||
| chr2:241437276
|
C | T | 5 | a0001c0004t0001g0178a0001c0004t0001g0179a0001c0004t0001g0180others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158+738C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437276 | ||||||
| chr2:241437364
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1158+826G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437364 | ||||||
| chr2:241437522
|
G | C | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158+984G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437522 | ||||||
| chr2:241437576
|
AT | A | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1040delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437576 | |||||
| chr2:241437580
|
C | G | 15 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0126others(12): Show | 15 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1158+1042C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437580 | ||||||
| chr2:241437648
|
A | ATATTTAT others(1): Show |
85 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(82): Show | 85 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1158+1128_1158+113 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437648 | |||||
| chr2:241437648
|
A | ATATTTAT others(5): Show |
3 | a0001c0001t0001g0287a0001c0001t0001g0316a0001c0001t0001g0333 | 3 | HG00735.hp2 HG03017.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1158+1124_1158+113 others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437648 | |||||
| chr2:241437648
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1158+1110A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437648 | ||||||
| chr2:241437652
|
T | A | 38 | a0001c0001t0009g0104a0001c0011t0001g0107a0001c0011t0001g0108others(35): Show | 38 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1158+1114T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437652 | ||||||
| chr2:241437658
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0343 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1158+1123_1158+112 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437658 | |||||
| chr2:241437662
|
A | ATTTTTTT others(2): Show |
17 | a0002c0002t0001g0200a0002c0002t0001g0257a0002c0002t0001g0335others(14): Show | 17 | HG00735.hp1 HG01081.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.1158+1127_1158+112 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437662 | |||||
| chr2:241437662
|
A | ATTTTTTT others(3): Show |
2 | a0002c0002t0001g0348a0002c0002t0001g0358 | 2 | HG01433.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1158+1127_1158+112 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437662 | |||||
| chr2:241437662
|
A | T | 6 | a0001c0015t0002g0371a0002c0002t0001g0258a0002c0002t0001g0259others(3): Show | 6 | HG00609.hp2 HG01256.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+1124A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437662 | ||||||
| chr2:241437664
|
T | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1158+1126T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437664 | ||||||
| chr2:241437666
|
A | AT | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(17): Show | 20 | HG00140.hp1 HG00423.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1158+1131dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437666 | |||||
| chr2:241437666
|
A | ATTTTTTT others(2): Show |
6 | a0001c0001t0001g0206a0002c0002t0001g0253a0002c0002t0001g0256others(3): Show | 6 | HG00597.hp1 HG00738.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+1131_1158+113 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437666 | |||||
| chr2:241437666
|
A | T | 39 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0215others(36): Show | 39 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1158+1128A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437666 | ||||||
| chr2:241437670
|
A | AT | 10 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0076others(7): Show | 10 | HG00280.hp2 HG00323.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1158+1144dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | |||||
| chr2:241437670
|
A | ATTTATTT others(2): Show |
6 | a0001c0006t0001g0244a0001c0006t0001g0245a0001c0006t0001g0246others(3): Show | 6 | HG00408.hp1 HG00597.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+1135_1158+113 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | |||||
| chr2:241437670
|
A | ATTTATTT others(1): Show |
6 | a0001c0001t0001g0209a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG01358.hp1 HG02027.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+1135_1158+113 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | |||||
| chr2:241437670
|
A | ATTTTTTT others(1): Show |
15 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(12): Show | 15 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1158+1137_1158+114 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241437670 | |||||
| chr2:241437670
|
A | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0001g0064others(105): Show | 108 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1158+1132A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437670 | ||||||
| chr2:241437674
|
T | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1158+1136T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437674 | ||||||
| chr2:241437677
|
T | A | 1 | a0001c0006t0001g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1158+1139T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437677 | ||||||
| chr2:241437759
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1158+1221T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437759 | ||||||
| chr2:241437809
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1158+1271T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437809 | ||||||
| chr2:241437825
|
T | C | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1158+1287T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437825 | ||||||
| chr2:241437856
|
G | A | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158+1318G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437856 | ||||||
| chr2:241437862
|
T | C | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158+1324T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437862 | ||||||
| chr2:241437911
|
C | T | 1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1158+1373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437911 | ||||||
| chr2:241437916
|
C | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1378C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437916 | ||||||
| chr2:241437941
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1158+1403A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437941 | ||||||
| chr2:241437963
|
C | G | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1158+1425C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437963 | ||||||
| chr2:241437964
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1158+1426C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241437964 | ||||||
| chr2:241438079
|
G | A | 1 | a0001c0001t0005g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1158+1541G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438079 | ||||||
| chr2:241438260
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1158+1722T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438260 | ||||||
| chr2:241438267
|
C | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1158+1729C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438267 | ||||||
| chr2:241438284
|
A | G | 286 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1158+1746A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438284 | ||||||
| chr2:241438371
|
A | G | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1158+1833A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438371 | ||||||
| chr2:241438405
|
A | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1158+1867A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438405 | ||||||
| chr2:241438486
|
G | A | 1 | a0008c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1158+1948G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438486 | ||||||
| chr2:241438547
|
A | C | 5 | a0001c0004t0001g0361a0001c0004t0001g0362a0001c0010t0001g0363others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158+2009A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438547 | ||||||
| chr2:241438581
|
G | T | 286 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1158+2043G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438581 | ||||||
| chr2:241438585
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1158+2047T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438585 | ||||||
| chr2:241438621
|
G | GT | 79 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(76): Show | 79 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1158+2095dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241438621 | |||||
| chr2:241438634
|
G | GT | 17 | a0001c0001t0001g0085a0001c0001t0001g0138a0001c0001t0001g0298others(14): Show | 17 | HG00140.hp1 HG02451.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1158+2109dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241438634 | |||||
| chr2:241438634
|
G | T | 4 | a0001c0001t0001g0378a0002c0002t0001g0354a0009c0012t0001g0001others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158+2096G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438634 | ||||||
| chr2:241438638
|
T | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1158+2100T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438638 | ||||||
| chr2:241438642
|
T | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1158+2104T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438642 | ||||||
| chr2:241438660
|
C | T | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1158+2122C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438660 | ||||||
| chr2:241438661
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1158+2123G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438661 | ||||||
| chr2:241438693
|
G | A | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1158+2155G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438693 | ||||||
| chr2:241438723
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1158+2185G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438723 | ||||||
| chr2:241438792
|
G | GC | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1158+2254_1158+225 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438792 | ||||||
| chr2:241438803
|
T | TG | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1158+2265_1158+226 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438803 | ||||||
| chr2:241438933
|
C | T | 25 | a0002c0002t0001g0200a0002c0002t0001g0335a0002c0002t0001g0336others(22): Show | 25 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1159-2371C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241438933 | ||||||
| chr2:241439169
|
C | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1159-2135C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439169 | ||||||
| chr2:241439178
|
G | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1159-2126G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439178 | ||||||
| chr2:241439179
|
C | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG03491.hp1 HG03492.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1159-2125C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439179 | ||||||
| chr2:241439339
|
C | A | 1 | a0005c0008t0001g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1159-1965C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439339 | ||||||
| chr2:241439490
|
T | C | 31 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(28): Show | 31 | HG00099.hp1 HG01123.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1159-1814T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439490 | ||||||
| chr2:241439531
|
G | A | 1 | a0001c0004t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1159-1773G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439531 | ||||||
| chr2:241439571
|
C | T | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1159-1733C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439571 | ||||||
| chr2:241439625
|
G | A | 7 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(4): Show | 7 | HG00609.hp1 HG02129.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159-1679G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439625 | ||||||
| chr2:241439732
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1159-1572C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439732 | ||||||
| chr2:241439831
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1159-1473G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439831 | ||||||
| chr2:241439833
|
G | C | 373 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(370): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1159-1471G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241439833 | ||||||
| chr2:241440222
|
G | A | 9 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159-1082G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440222 | ||||||
| chr2:241440278
|
G | A | 3 | a0001c0010t0001g0363a0001c0010t0001g0364a0001c0010t0001g0365 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1159-1026G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440278 | ||||||
| chr2:241440336
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1159-968G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440336 | ||||||
| chr2:241440371
|
C | T | 1 | a0008c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159-933C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440371 | ||||||
| chr2:241440380
|
G | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1159-924G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440380 | ||||||
| chr2:241440512
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1159-792A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440512 | ||||||
| chr2:241440967
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1159-337T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241440967 | ||||||
| chr2:241441021
|
TG | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1159-282delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241441021 | ||||||
| chr2:241441057
|
T | C | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1159-247T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | chr2 | 241441057 | ||||||
| chr2:241441074
|
G | GA | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1159-223dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 241441074 | |||||
| chr2:241441561
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.1411+5C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241441561 | ||||||
| chr2:241441733
|
C | T | 2 | a0002c0002t0001g0200a0002c0002t0001g0358 | 2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1411+177C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241441733 | ||||||
| chr2:241442142
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1411+586T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442142 | ||||||
| chr2:241442718
|
C | T | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+1162C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442718 | ||||||
| chr2:241442732
|
C | G | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411+1176C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442732 | ||||||
| chr2:241442735
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+1179C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442735 | ||||||
| chr2:241442777
|
C | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1411+1221C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442777 | ||||||
| chr2:241442816
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1411+1260G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442816 | ||||||
| chr2:241442886
|
A | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+1330A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241442886 | ||||||
| chr2:241443104
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1411+1548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443104 | ||||||
| chr2:241443191
|
A | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(93): Show | 96 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1411+1635A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443191 | ||||||
| chr2:241443242
|
A | G | 1 | a0001c0003t0001g0007 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1411+1686A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443242 | ||||||
| chr2:241443291
|
A | G | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1411+1735A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443291 | ||||||
| chr2:241443301
|
T | C | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1411+1745T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443301 | ||||||
| chr2:241443449
|
C | T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1411+1893C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443449 | ||||||
| chr2:241443563
|
G | A | 1 | a0002c0002t0001g0341 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1411+2007G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443563 | ||||||
| chr2:241443671
|
A | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1411+2115A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443671 | ||||||
| chr2:241443703
|
G | GCC | 4 | a0001c0003t0001g0011a0001c0003t0001g0012a0001c0003t0001g0013others(1): Show | 4 | NA18954.hp1 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411+2148_1411+214 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241443703 | |||||
| chr2:241443875
|
A | C | 11 | a0004c0007t0001g0096a0004c0007t0001g0097a0004c0007t0001g0100others(8): Show | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+2319A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443875 | ||||||
| chr2:241443985
|
C | G | 4 | a0003c0005t0001g0192a0003c0005t0001g0198a0003c0005t0001g0199others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+2429C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241443985 | ||||||
| chr2:241444080
|
G | A | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1411+2524G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444080 | ||||||
| chr2:241444134
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1411+2578T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444134 | ||||||
| chr2:241444168
|
TTGA | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1411+2615_1411+261 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241444168 | |||||
| chr2:241444332
|
G | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+2776G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444332 | ||||||
| chr2:241444513
|
G | T | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1411+2957G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444513 | ||||||
| chr2:241444639
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+3083A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444639 | ||||||
| chr2:241444660
|
G | A | 1 | a0012c0023t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1411+3104G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444660 | ||||||
| chr2:241444696
|
G | A | 3 | a0005c0008t0001g0147a0005c0008t0001g0150a0005c0014t0001g0149 | 3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1411+3140G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444696 | ||||||
| chr2:241444732
|
G | T | 7 | a0001c0004t0001g0359a0001c0004t0001g0360a0001c0004t0001g0361others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411+3176G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444732 | ||||||
| chr2:241444779
|
C | G | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1411+3223C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444779 | ||||||
| chr2:241444893
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3337T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444893 | ||||||
| chr2:241444899
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3343C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444899 | ||||||
| chr2:241444900
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1411+3344T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444900 | ||||||
| chr2:241444953
|
G | A | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1411+3397G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444953 | ||||||
| chr2:241444983
|
A | C | 1 | a0005c0008t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1411+3427A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241444983 | ||||||
| chr2:241445043
|
C | T | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1411+3487C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445043 | ||||||
| chr2:241445087
|
G | A | 1 | a0005c0008t0001g0152 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1411+3531G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445087 | ||||||
| chr2:241445160
|
G | A | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1411+3604G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445160 | ||||||
| chr2:241445166
|
C | A | 274 | a0001c0001t0001g0004a0001c0001t0001g0158a0001c0001t0001g0201others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1411+3610C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445166 | ||||||
| chr2:241445166
|
C | G | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+3610C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445166 | ||||||
| chr2:241445212
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+3656A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445212 | ||||||
| chr2:241445244
|
C | CA | 124 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0065others(121): Show | 124 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1411+3708dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | |||||
| chr2:241445244
|
C | CAA | 128 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0070others(125): Show | 128 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1411+3707_1411+370 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | |||||
| chr2:241445244
|
C | CAAA | 11 | a0001c0001t0001g0103a0001c0001t0001g0269a0001c0001t0001g0288others(8): Show | 11 | HG01934.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411+3706_1411+370 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241445244 | |||||
| chr2:241445320
|
G | T | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+3764G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445320 | ||||||
| chr2:241445377
|
G | T | 1 | a0001c0003t0008g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1411+3821G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445377 | ||||||
| chr2:241445380
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+3824G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445380 | ||||||
| chr2:241445428
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1411+3872C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445428 | ||||||
| chr2:241445561
|
T | C | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+4005T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445561 | ||||||
| chr2:241445851
|
A | C | 11 | a0004c0007t0001g0096a0004c0007t0001g0097a0004c0007t0001g0100others(8): Show | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+4295A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445851 | ||||||
| chr2:241445925
|
A | G | 89 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(86): Show | 89 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1411+4369A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241445925 | ||||||
| chr2:241446497
|
G | GGAGTAAT others(6): Show |
1 | a0004c0007t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1411+4942_1411+495 others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241446497 | |||||
| chr2:241446600
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5044A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446600 | ||||||
| chr2:241446601
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5045A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446601 | ||||||
| chr2:241446640
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+5084C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446640 | ||||||
| chr2:241446685
|
A | T | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1411+5129A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446685 | ||||||
| chr2:241446738
|
T | TC | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411+5182_1411+518 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446738 | ||||||
| chr2:241446765
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1411+5209T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241446765 | ||||||
| chr2:241447167
|
T | C | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411+5611T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447167 | ||||||
| chr2:241447239
|
A | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+5683A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447239 | ||||||
| chr2:241447455
|
C | T | 30 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1411+5899C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447455 | ||||||
| chr2:241447464
|
C | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1411+5908C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447464 | ||||||
| chr2:241447931
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(84): Show | 87 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1411+6375G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241447931 | ||||||
| chr2:241448283
|
A | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1411+6727A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448283 | ||||||
| chr2:241448371
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0224 | 2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1411+6815A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448371 | ||||||
| chr2:241448407
|
G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1411+6851G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448407 | ||||||
| chr2:241448527
|
A | G | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1411+6971A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448527 | ||||||
| chr2:241448569
|
A | G | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1411+7013A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448569 | ||||||
| chr2:241448599
|
A | C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1411+7043A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448599 | ||||||
| chr2:241448756
|
C | A | 1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1411+7200C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448756 | ||||||
| chr2:241448810
|
G | T | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1411+7254G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241448810 | ||||||
| chr2:241449015
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18961.hp2 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1411+7459G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449015 | ||||||
| chr2:241449048
|
T | G | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1411+7492T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449048 | ||||||
| chr2:241449094
|
C | T | 3 | a0001c0001t0002g0372a0001c0001t0002g0374a0001c0015t0002g0371 | 3 | HG01261.hp2 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1411+7538C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449094 | ||||||
| chr2:241449135
|
T | C | 287 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0158others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1411+7579T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449135 | ||||||
| chr2:241449270
|
G | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1412-7477G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449270 | ||||||
| chr2:241449289
|
G | C | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1412-7458G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449289 | ||||||
| chr2:241449375
|
G | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0158others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1412-7372G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449375 | ||||||
| chr2:241449388
|
A | G | 2 | a0001c0001t0001g0142a0001c0004t0001g0143 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1412-7359A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449388 | ||||||
| chr2:241449412
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1412-7335G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449412 | ||||||
| chr2:241449515
|
CTT | C | 31 | a0001c0001t0001g0158a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-7230_1412-722 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241449515 | |||||
| chr2:241449694
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1412-7053G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449694 | ||||||
| chr2:241449725
|
G | A | 1 | a0005c0008t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1412-7022G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449725 | ||||||
| chr2:241449766
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1412-6981A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449766 | ||||||
| chr2:241449811
|
A | G | 88 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0202others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1412-6936A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449811 | ||||||
| chr2:241449867
|
C | T | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1412-6880C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449867 | ||||||
| chr2:241449876
|
G | A | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-6871G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449876 | ||||||
| chr2:241449880
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1412-6867G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449880 | ||||||
| chr2:241449942
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1412-6805G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241449942 | ||||||
| chr2:241450101
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1412-6646G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450101 | ||||||
| chr2:241450312
|
A | G | 10 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0147others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-6435A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450312 | ||||||
| chr2:241450415
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1412-6332C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450415 | ||||||
| chr2:241450450
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-6297G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450450 | ||||||
| chr2:241450450
|
G | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0136others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1412-6297G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450450 | ||||||
| chr2:241450557
|
TCAGGAGG others(1244): Show |
T | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1412-6186_1412-493 others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241450557 | |||||
| chr2:241450591
|
A | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-6156A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450591 | ||||||
| chr2:241450640
|
C | T | 1 | a0001c0006t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1412-6107C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450640 | ||||||
| chr2:241450995
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1412-5752T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241450995 | ||||||
| chr2:241451066
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-5681C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451066 | ||||||
| chr2:241451081
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1412-5666T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451081 | ||||||
| chr2:241451111
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | NA18966.hp2 NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1412-5636C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451111 | ||||||
| chr2:241451554
|
T | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-5193T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451554 | ||||||
| chr2:241451647
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01070.hp2 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-5100G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451647 | ||||||
| chr2:241451660
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1412-5087A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451660 | ||||||
| chr2:241451676
|
T | C | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1412-5071T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451676 | ||||||
| chr2:241451741
|
T | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(2): Show | 5 | NA18953.hp1 NA19000.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-5006T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451741 | ||||||
| chr2:241451752
|
T | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-4995T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451752 | ||||||
| chr2:241451762
|
T | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02559.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1412-4985T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451762 | ||||||
| chr2:241451768
|
T | G | 58 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1412-4979T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451768 | ||||||
| chr2:241451797
|
C | T | 58 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1412-4950C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451797 | ||||||
| chr2:241451817
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1412-4930C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451817 | ||||||
| chr2:241451818
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1412-4929G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451818 | ||||||
| chr2:241451885
|
G | A | 5 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(2): Show | 5 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-4862G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451885 | ||||||
| chr2:241451994
|
A | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0126others(15): Show | 18 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1412-4753A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241451994 | ||||||
| chr2:241452203
|
A | G | 1 | a0001c0004t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1412-4544A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452203 | ||||||
| chr2:241452287
|
C | T | 1 | a0001c0004t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1412-4460C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452287 | ||||||
| chr2:241452425
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1412-4322A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452425 | ||||||
| chr2:241452643
|
A | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-4104A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452643 | ||||||
| chr2:241452815
|
T | C | 287 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0158others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1412-3932T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452815 | ||||||
| chr2:241452848
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1412-3899C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452848 | ||||||
| chr2:241452937
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1412-3810G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241452937 | ||||||
| chr2:241452942
|
CA | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG01167.hp1 HG01168.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-3793delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241452942 | |||||
| chr2:241453052
|
C | T | 1 | a0005c0008t0001g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1412-3695C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453052 | ||||||
| chr2:241453058
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3689G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453058 | ||||||
| chr2:241453099
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-3648G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453099 | ||||||
| chr2:241453135
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1412-3612A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453135 | ||||||
| chr2:241453139
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1412-3608G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453139 | ||||||
| chr2:241453236
|
A | G | 42 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0237others(39): Show | 42 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412-3511A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453236 | ||||||
| chr2:241453278
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1412-3469C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453278 | ||||||
| chr2:241453312
|
A | G | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1412-3435A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453312 | ||||||
| chr2:241453344
|
T | C | 28 | a0001c0001t0001g0142a0001c0003t0001g0054a0001c0003t0001g0056others(25): Show | 28 | HG00099.hp1 HG00642.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.1412-3403T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453344 | ||||||
| chr2:241453360
|
T | C | 123 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(120): Show | 123 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1412-3387T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453360 | ||||||
| chr2:241453388
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3359C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453388 | ||||||
| chr2:241453389
|
A | G | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3358A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453389 | ||||||
| chr2:241453393
|
C | T | 5 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(2): Show | 5 | HG02132.hp1 HG02135.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-3354C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453393 | ||||||
| chr2:241453397
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3350C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453397 | ||||||
| chr2:241453398
|
A | G | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1412-3349A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453398 | ||||||
| chr2:241453418
|
C | A | 2 | a0001c0004t0001g0164a0003c0005t0001g0369 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1412-3329C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453418 | ||||||
| chr2:241453418
|
C | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1412-3329C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453418 | ||||||
| chr2:241453426
|
T | C | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1412-3321T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453426 | ||||||
| chr2:241453433
|
T | C | 33 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.1412-3314T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453433 | ||||||
| chr2:241453438
|
T | C | 96 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1412-3309T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453438 | ||||||
| chr2:241453439
|
G | A | 40 | a0001c0001t0001g0142a0001c0001t0001g0158a0001c0001t0001g0304others(37): Show | 40 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1412-3308G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453439 | ||||||
| chr2:241453443
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1412-3304A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453443 | ||||||
| chr2:241453447
|
C | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0327 | 3 | HG01928.hp2 HG01975.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1412-3300C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453447 | ||||||
| chr2:241453449
|
C | T | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1412-3298C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453449 | ||||||
| chr2:241453450
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1412-3297G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453450 | ||||||
| chr2:241453451
|
T | C | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0280 | 3 | HG01928.hp2 HG01975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1412-3296T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453451 | ||||||
| chr2:241453494
|
A | C | 4 | a0001c0001t0001g0271a0001c0006t0001g0246a0009c0012t0001g0001others(1): Show | 4 | HG02630.hp2 HG02698.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-3253A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453494 | ||||||
| chr2:241453539
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3208A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453539 | ||||||
| chr2:241453546
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3201T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453546 | ||||||
| chr2:241453553
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1412-3194C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453553 | ||||||
| chr2:241453603
|
A | C | 3 | a0008c0021t0003g0334a0009c0012t0001g0001a0009c0012t0001g0002 | 3 | HG00140.hp2 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1412-3144A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453603 | ||||||
| chr2:241453609
|
G | A | 1 | a0008c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1412-3138G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453609 | ||||||
| chr2:241453621
|
C | CA | 32 | a0001c0001t0001g0228a0001c0003t0001g0007a0001c0003t0001g0009others(29): Show | 32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1412-3113dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453621 | |||||
| chr2:241453672
|
C | T | 20 | a0001c0001t0001g0158a0001c0004t0001g0143a0001c0004t0001g0157others(17): Show | 20 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1412-3075C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453672 | ||||||
| chr2:241453768
|
GGTT | G | 17 | a0001c0004t0001g0370a0001c0006t0001g0240a0001c0006t0001g0241others(14): Show | 17 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | ||||||
| chr2:241453768
|
GGTTT | G | 35 | a0001c0004t0001g0359a0001c0006t0001g0236a0001c0006t0001g0242others(32): Show | 35 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | ||||||
| chr2:241453768
|
GGTTTT | G | 21 | a0001c0001t0001g0136a0001c0001t0001g0208a0001c0001t0001g0209others(18): Show | 21 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | ||||||
| chr2:241453768
|
GGTTTTT | G | 43 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(40): Show | 43 | HG00423.hp2 HG00639.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | ||||||
| chr2:241453768
|
GGTTTTTT | G | 46 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0012others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1412-2978_1412-297 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453768 | ||||||
| chr2:241453769
|
G | GT | 17 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0110others(14): Show | 17 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1412-2946dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453769
|
G | GTT | 6 | a0001c0001t0001g0103a0001c0001t0001g0378a0001c0001t0002g0372others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-2947_1412-294 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453769
|
G | GTTTTT | 11 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1412-2950_1412-294 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453769
|
G | GTTTTTT | 16 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0070others(13): Show | 16 | HG00423.hp1 HG01934.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1412-2951_1412-294 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453769
|
GTT | G | 33 | a0001c0001t0001g0231a0001c0001t0001g0237a0001c0001t0001g0262others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1412-2947_1412-294 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453769
|
GTTT | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0158others(79): Show | 82 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1412-2948_1412-294 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453769 | |||||
| chr2:241453775
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1412-2972T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453775 | ||||||
| chr2:241453780
|
T | G | 1 | a0001c0003t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1412-2967T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453780 | ||||||
| chr2:241453848
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1412-2899A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453848 | ||||||
| chr2:241453885
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | NA18966.hp2 NA18979.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1412-2862G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241453885 | ||||||
| chr2:241453958
|
AT | A | 284 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0142others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1412-2782delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241453958 | |||||
| chr2:241454081
|
G | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0377 | 2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1412-2666G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454081 | ||||||
| chr2:241454159
|
T | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0142others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1412-2588T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454159 | ||||||
| chr2:241454212
|
C | T | 5 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0042others(2): Show | 5 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-2535C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454212 | ||||||
| chr2:241454243
|
A | C | 49 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(46): Show | 49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1412-2504A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454243 | ||||||
| chr2:241454380
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(198): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.1412-2367G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454380 | ||||||
| chr2:241454383
|
A | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(119): Show | 122 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1412-2364A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454383 | ||||||
| chr2:241454455
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0131others(2): Show | 5 | HG01099.hp2 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1412-2292G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454455 | ||||||
| chr2:241454468
|
A | G | 10 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412-2279A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454468 | ||||||
| chr2:241454588
|
T | C | 32 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1412-2159T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454588 | ||||||
| chr2:241454726
|
G | T | 193 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0142others(190): Show | 193 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1412-2021G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454726 | ||||||
| chr2:241454727
|
G | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1412-2020G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454727 | ||||||
| chr2:241454807
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1412-1940A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454807 | ||||||
| chr2:241454971
|
C | T | 1 | a0001c0022t0001g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1412-1776C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454971 | ||||||
| chr2:241454973
|
C | G | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1412-1774C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241454973 | ||||||
| chr2:241455150
|
A | G | 1 | a0001c0006t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1412-1597A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455150 | ||||||
| chr2:241455309
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-1438A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455309 | ||||||
| chr2:241455452
|
C | T | 1 | a0003c0005t0001g0057 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1412-1295C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455452 | ||||||
| chr2:241455541
|
C | T | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-1206C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455541 | ||||||
| chr2:241455735
|
C | CT | 74 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0220others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1412-990dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | |||||
| chr2:241455735
|
C | CTT | 30 | a0001c0003t0001g0031a0001c0003t0001g0033a0001c0003t0007g0036others(27): Show | 30 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1412-991_1412-990d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | |||||
| chr2:241455735
|
CT | C | 72 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1412-990delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | |||||
| chr2:241455735
|
CTTTTTTT | C | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1412-996_1412-990d others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455735 | |||||
| chr2:241455900
|
C | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1412-847C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455900 | ||||||
| chr2:241455940
|
C | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1412-807C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241455940 | ||||||
| chr2:241455999
|
T | TAGAAAAA others(1578): Show |
2 | a0006c0009t0001g0183a0006c0009t0001g0184 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1412-729_1412-728i others(1587): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 241455999 | |||||
| chr2:241456108
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-639A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456108 | ||||||
| chr2:241456139
|
A | G | 70 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1412-608A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456139 | ||||||
| chr2:241456171
|
T | G | 36 | a0001c0001t0001g0136a0001c0001t0001g0158a0001c0004t0001g0143others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1412-576T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456171 | ||||||
| chr2:241456259
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0142others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1412-488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456259 | ||||||
| chr2:241456376
|
G | A | 2 | a0001c0004t0001g0175a0001c0004t0001g0359 | 2 | HG02257.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1412-371G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456376 | ||||||
| chr2:241456412
|
T | A | 1 | a0001c0003t0001g0015 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1412-335T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456412 | ||||||
| chr2:241456503
|
G | C | 31 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-244G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456503 | ||||||
| chr2:241456618
|
A | G | 64 | a0001c0001t0001g0136a0001c0001t0001g0158a0001c0001t0001g0205others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1412-129A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456618 | ||||||
| chr2:241456672
|
A | T | 113 | a0001c0001t0001g0136a0001c0001t0001g0158a0001c0001t0001g0205others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1412-75A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456672 | ||||||
| chr2:241456680
|
C | T | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1412-67C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456680 | ||||||
| chr2:241456731
|
C | T | 2 | a0001c0004t0001g0168a0001c0004t0001g0176 | 2 | HG02895.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1412-16C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 13/26 | chr2 | 241456731 | ||||||
| chr2:241456966
|
G | A | 3 | a0004c0007t0001g0096a0004c0007t0001g0097a0004c0007t0001g0106 | 3 | HG01099.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1587+44G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241456966 | ||||||
| chr2:241457011
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0231others(56): Show | 59 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1587+89G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457011 | ||||||
| chr2:241457016
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1587+94G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457016 | ||||||
| chr2:241457097
|
A | G | 3 | a0001c0001t0001g0098a0001c0003t0001g0038a0005c0014t0001g0149 | 3 | HG03098.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1587+175A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457097 | ||||||
| chr2:241457156
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1587+234G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457156 | ||||||
| chr2:241457251
|
T | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(198): Show | 201 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1587+329T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457251 | ||||||
| chr2:241457260
|
T | G | 1 | a0001c0011t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1587+338T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457260 | ||||||
| chr2:241457275
|
CCCGT | C | 4 | a0003c0005t0001g0369a0007c0013t0001g0191a0009c0012t0001g0001others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+356_1587+359d others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457275 | |||||
| chr2:241457278
|
G | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0098others(170): Show | 173 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.1587+356G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457278 | ||||||
| chr2:241457279
|
T | C | 150 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0098others(147): Show | 150 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1587+357T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457279 | ||||||
| chr2:241457337
|
T | C | 1 | a0001c0006t0001g0236 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1587+415T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457337 | ||||||
| chr2:241457351
|
G | GGAAAGAT others(74): Show |
3 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017 | 3 | HG00609.hp1 HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1587+466_1587+467i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | |||||
| chr2:241457351
|
G | GGAAAGAT others(74): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+466_1587+467i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | |||||
| chr2:241457351
|
G | GGAAAGAT others(74): Show |
2 | a0001c0004t0001g0359a0011c0020t0001g0155 | 2 | HG00323.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1587+456_1587+536d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457351 | |||||
| chr2:241457356
|
GATCTGGG others(398): Show |
G | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204others(6): Show | 9 | HG01081.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587+467_1587+871d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457356 | |||||
| chr2:241457378
|
G | A | 7 | a0001c0001t0001g0103a0001c0025t0001g0160a0005c0008t0001g0146others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1587+456G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457378 | ||||||
| chr2:241457378
|
GCACTAGG others(74): Show |
G | 32 | a0001c0001t0001g0123a0001c0001t0001g0136a0001c0003t0001g0007others(29): Show | 32 | HG00280.hp1 HG01106.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1587+467_1587+547d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457378 | |||||
| chr2:241457378
|
GCACTAGG others(236): Show |
G | 5 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(2): Show | 5 | HG00642.hp2 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+467_1587+709d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457378 | |||||
| chr2:241457389
|
T | C | 54 | a0001c0001t0001g0067a0001c0001t0001g0092a0001c0001t0001g0103others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1587+467T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457389 | ||||||
| chr2:241457389
|
T | TGCTTTGG others(155): Show |
1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1587+495_1587+496i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | |||||
| chr2:241457389
|
T | TGCTTTGG others(155): Show |
1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1587+495_1587+496i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | |||||
| chr2:241457389
|
TGCTTTGG others(74): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1587+496_1587+576d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457389 | |||||
| chr2:241457402
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1587+480G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457402 | ||||||
| chr2:241457402
|
G | GGAGAGGC others(74): Show |
2 | a0001c0001t0002g0372a0001c0015t0002g0371 | 2 | HG01261.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1587+495_1587+496i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457402 | |||||
| chr2:241457402
|
G | GGAGAGGC others(398): Show |
2 | a0001c0001t0002g0373a0001c0001t0002g0375 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1587+495_1587+496i others(407): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457402 | |||||
| chr2:241457418
|
A | G | 22 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0287others(19): Show | 22 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1587+496A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457418 | ||||||
| chr2:241457423
|
G | A | 19 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0287others(16): Show | 19 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1587+501G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457423 | ||||||
| chr2:241457423
|
G | GCCCAGTG others(155): Show |
1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1587+624_1587+785d others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
G | GCCCAGTG others(155): Show |
2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1587+536_1587+537i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
G | GCCCAGTG others(236): Show |
1 | a0003c0005t0001g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
G | GCCCAGTG others(317): Show |
1 | a0005c0014t0001g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1587+536_1587+537i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
G | GCCCAGTG others(74): Show |
3 | a0001c0010t0001g0363a0001c0010t0001g0364a0001c0010t0001g0365 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1587+536_1587+537i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
G | GCCCAGTG others(236): Show |
5 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0042others(2): Show | 5 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457423
|
GCCCAGTG others(155): Show |
G | 11 | a0001c0006t0001g0240a0001c0006t0001g0241a0001c0006t0001g0242others(8): Show | 11 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+624_1587+785d others(2): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457423 | |||||
| chr2:241457437
|
G | C | 6 | a0001c0001t0001g0103a0001c0025t0001g0160a0005c0008t0001g0147others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+515G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457437 | ||||||
| chr2:241457437
|
G | GATCTGGG others(155): Show |
1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1587+536_1587+537i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457437 | |||||
| chr2:241457459
|
A | ACACTAGG others(155): Show |
1 | a0001c0001t0001g0212 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1587+617_1587+618i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | |||||
| chr2:241457459
|
A | ACACTAGG others(74): Show |
1 | a0001c0004t0001g0359 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1587+618_1587+698d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | |||||
| chr2:241457459
|
A | ACACTAGG others(155): Show |
1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1587+559_1587+560i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | |||||
| chr2:241457459
|
A | ACACTAGG others(74): Show |
2 | a0001c0001t0001g0113a0010c0026t0001g0116 | 2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1587+547_1587+548i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | |||||
| chr2:241457459
|
A | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1587+537A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457459 | ||||||
| chr2:241457459
|
A | GCACTAGG others(236): Show |
1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1587+536_1587+537i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457459 | ||||||
| chr2:241457459
|
ACACTAGG others(74): Show |
A | 1 | a0001c0006t0001g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1587+618_1587+698d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457459 | |||||
| chr2:241457465
|
G | GGGACTGC others(722): Show |
1 | a0002c0002t0001g0345 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1587+547_1587+548i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457465 | |||||
| chr2:241457470
|
C | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0113a0001c0001t0001g0142others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1587+548C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457470 | ||||||
| chr2:241457470
|
C | TGCTTTGG others(155): Show |
2 | a0001c0001t0002g0374a0007c0013t0001g0028 | 2 | HG02559.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1587+547_1587+548i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457470 | ||||||
| chr2:241457482
|
C | T | 2 | a0001c0001t0001g0378a0002c0002t0001g0345 | 2 | HG01975.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1587+560C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457482 | ||||||
| chr2:241457483
|
G | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0142others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1587+561G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457483 | ||||||
| chr2:241457483
|
G | GGAGAGGC others(74): Show |
1 | a0001c0001t0001g0287 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1587+576_1587+577i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457483 | |||||
| chr2:241457499
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0142others(82): Show | 85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1587+577G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457499 | ||||||
| chr2:241457504
|
A | ACCCAGTG others(722): Show |
3 | a0002c0002t0001g0200a0002c0002t0001g0358a0014c0018t0001g0339 | 3 | NA18960.hp1 NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1587+617_1587+618i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | |||||
| chr2:241457504
|
A | ACCCAGTG others(2342): Show |
1 | a0002c0002t0001g0258 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1587+617_1587+618i others(2351): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | |||||
| chr2:241457504
|
A | ACCCAGTG others(74): Show |
1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587+628_1587+629i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457504 | |||||
| chr2:241457504
|
A | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0142others(82): Show | 85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1587+582A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457504 | ||||||
| chr2:241457518
|
G | C | 4 | a0001c0001t0001g0072a0005c0008t0001g0144a0005c0008t0001g0146others(1): Show | 4 | HG02074.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+596G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457518 | ||||||
| chr2:241457518
|
G | GATCTGGG others(317): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0318 | 2 | NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1587+657_1587+658i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457518 | |||||
| chr2:241457518
|
G | GATCTGGG others(74): Show |
24 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.1587+676_1587+677i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457518 | |||||
| chr2:241457540
|
G | A | 44 | a0001c0001t0001g0189a0001c0001t0001g0205a0001c0001t0001g0206others(41): Show | 44 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1587+618G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457540 | ||||||
| chr2:241457540
|
G | GCACTAAG others(317): Show |
2 | a0002c0002t0001g0348a0002c0002t0001g0350 | 2 | HG01256.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1587+623_1587+624i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAAG others(803): Show |
1 | a0002c0002t0001g0253 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1587+623_1587+624i others(812): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAAG others(722): Show |
5 | a0002c0002t0001g0254a0002c0002t0001g0260a0002c0002t0001g0261others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+623_1587+624i others(731): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAAG others(641): Show |
20 | a0002c0002t0001g0256a0002c0002t0001g0257a0002c0002t0001g0259others(17): Show | 20 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1587+623_1587+624i others(650): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAAG others(642): Show |
1 | a0002c0002t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1587+623_1587+624i others(651): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAAG others(236): Show |
2 | a0002c0002t0001g0336a0002c0002t0001g0353 | 2 | NA18952.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1587+623_1587+624i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
G | GCACTAGG others(560): Show |
2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1587+657_1587+658i others(569): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457540
|
GCACTAGG others(74): Show |
G | 5 | a0001c0001t0001g0005a0001c0001t0001g0093a0001c0001t0001g0098others(2): Show | 5 | HG02486.hp1 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+699_1587+779d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457540 | |||||
| chr2:241457546
|
G | A | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+624G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457546 | ||||||
| chr2:241457546
|
G | GGGACCGC others(74): Show |
1 | a0008c0028t0001g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457546 | |||||
| chr2:241457546
|
G | GGGACCGC others(236): Show |
1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1587+698_1587+699i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457546 | |||||
| chr2:241457551
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0378 | 2 | HG01167.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1587+629C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457551 | ||||||
| chr2:241457563
|
C | CGGAGAGG others(155): Show |
1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+698_1587+699i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457563 | |||||
| chr2:241457563
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1587+641C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457563 | ||||||
| chr2:241457573
|
C | T | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587+651C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457573 | ||||||
| chr2:241457580
|
G | A | 33 | a0001c0001t0001g0378a0001c0003t0001g0007a0001c0003t0001g0009others(30): Show | 33 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587+658G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457580 | ||||||
| chr2:241457585
|
A | ACCCAGTG others(74): Show |
2 | a0001c0004t0001g0143a0001c0004t0001g0362 | 2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | |||||
| chr2:241457585
|
A | ACCCAGTG others(155): Show |
17 | a0001c0004t0001g0157a0001c0004t0001g0159a0001c0004t0001g0161others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.1587+698_1587+699i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | |||||
| chr2:241457585
|
A | ACCCAGTG others(74): Show |
3 | a0001c0010t0001g0363a0001c0010t0001g0364a0001c0010t0001g0365 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1587+698_1587+699i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457585 | |||||
| chr2:241457585
|
A | G | 40 | a0001c0001t0001g0378a0001c0003t0001g0007a0001c0003t0001g0009others(37): Show | 40 | HG00280.hp1 HG00609.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1587+663A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457585 | ||||||
| chr2:241457621
|
A | ACACTAGG others(74): Show |
3 | a0005c0008t0001g0144a0005c0008t0001g0146a0005c0008t0001g0154 | 3 | HG02647.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1587+705_1587+785d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457621 | |||||
| chr2:241457621
|
A | ACACTAGG others(317): Show |
1 | a0004c0007t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1587+785_1587+786i others(326): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457621 | |||||
| chr2:241457621
|
A | G | 289 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1587+699A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457621 | ||||||
| chr2:241457627
|
G | A | 38 | a0001c0004t0001g0361a0002c0002t0001g0200a0002c0002t0001g0253others(35): Show | 38 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1587+705G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457627 | ||||||
| chr2:241457644
|
C | T | 4 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056others(1): Show | 4 | HG00642.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+722C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457644 | ||||||
| chr2:241457644
|
CGGAGAGG others(74): Show |
C | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1587+758_1587+838d others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457644 | |||||
| chr2:241457654
|
C | CTTGGGCG others(155): Show |
21 | a0003c0005t0001g0008a0003c0005t0001g0040a0003c0005t0001g0043others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1587+779_1587+780i others(164): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | |||||
| chr2:241457654
|
C | CTTGGGCG others(236): Show |
1 | a0003c0005t0001g0044 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1587+785_1587+786i others(245): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | |||||
| chr2:241457654
|
C | CTTGGGCG others(74): Show |
2 | a0003c0005t0001g0051a0003c0005t0001g0194 | 2 | HG01934.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1587+785_1587+786i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457654 | |||||
| chr2:241457654
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0142others(93): Show | 96 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1587+732C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457654 | ||||||
| chr2:241457661
|
G | A | 2 | a0001c0004t0001g0361a0001c0004t0001g0370 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1587+739G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457661 | ||||||
| chr2:241457666
|
A | G | 2 | a0001c0004t0001g0361a0001c0004t0001g0370 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1587+744A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457666 | ||||||
| chr2:241457680
|
G | C | 5 | a0001c0001t0001g0158a0001c0003t0001g0011a0001c0003t0001g0012others(2): Show | 5 | HG02622.hp2 NA18954.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587+758G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457680 | ||||||
| chr2:241457702
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+780G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457702 | ||||||
| chr2:241457708
|
A | AGGACCGC others(74): Show |
1 | a0001c0001t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1587+802_1587+803i others(83): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241457708 | |||||
| chr2:241457708
|
A | G | 76 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1587+786A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457708 | ||||||
| chr2:241457725
|
T | C | 7 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(4): Show | 7 | HG00642.hp2 HG01243.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+803T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457725 | ||||||
| chr2:241457742
|
G | A | 4 | a0001c0001t0001g0158a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+820G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457742 | ||||||
| chr2:241457747
|
A | G | 4 | a0001c0001t0001g0158a0001c0003t0001g0054a0001c0003t0001g0055others(1): Show | 4 | HG00642.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587+825A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457747 | ||||||
| chr2:241457761
|
C | G | 7 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056others(4): Show | 7 | HG00642.hp2 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+839C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457761 | ||||||
| chr2:241457789
|
G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1587+867G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457789 | ||||||
| chr2:241457795
|
G | A | 35 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(32): Show | 35 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1587+873G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457795 | ||||||
| chr2:241457822
|
C | T | 24 | a0001c0001t0001g0268a0001c0001t0001g0304a0001c0001t0001g0305others(21): Show | 24 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1587+900C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457822 | ||||||
| chr2:241457877
|
G | A | 256 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(253): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1587+955G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457877 | ||||||
| chr2:241457904
|
A | C | 286 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1587+982A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457904 | ||||||
| chr2:241457960
|
G | A | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1587+1038G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241457960 | ||||||
| chr2:241458029
|
A | G | 13 | a0001c0006t0001g0236a0001c0006t0001g0240a0001c0006t0001g0241others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1587+1107A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458029 | ||||||
| chr2:241458045
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1587+1123A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458045 | ||||||
| chr2:241458326
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1587+1404G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458326 | ||||||
| chr2:241458336
|
A | G | 2 | a0006c0009t0001g0183a0006c0009t0001g0184 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1587+1414A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458336 | ||||||
| chr2:241458355
|
G | A | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1587+1433G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458355 | ||||||
| chr2:241458411
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1587+1489G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458411 | ||||||
| chr2:241458449
|
G | A | 1 | a0002c0002t0001g0341 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1587+1527G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458449 | ||||||
| chr2:241458601
|
G | A | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1587+1679G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458601 | ||||||
| chr2:241458659
|
T | C | 31 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1587+1737T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458659 | ||||||
| chr2:241458681
|
C | CA | 57 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0006t0001g0236others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1587+1770dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241458681 | |||||
| chr2:241458970
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1587+2048G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241458970 | ||||||
| chr2:241459108
|
G | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1587+2186G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459108 | ||||||
| chr2:241459262
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1587+2340C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459262 | ||||||
| chr2:241459281
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1587+2359G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459281 | ||||||
| chr2:241459349
|
C | T | 1 | a0005c0008t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1587+2427C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459349 | ||||||
| chr2:241459454
|
C | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1587+2532C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459454 | ||||||
| chr2:241459460
|
C | T | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1587+2538C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459460 | ||||||
| chr2:241459658
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587+2736T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459658 | ||||||
| chr2:241459682
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1587+2760C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459682 | ||||||
| chr2:241459708
|
C | T | 1 | a0003c0005t0001g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1587+2786C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459708 | ||||||
| chr2:241459720
|
G | T | 1 | a0001c0006t0001g0245 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1587+2798G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459720 | ||||||
| chr2:241459839
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1588-2684G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459839 | ||||||
| chr2:241459860
|
C | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1588-2663C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241459860 | ||||||
| chr2:241460030
|
A | G | 32 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(29): Show | 32 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-2493A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460030 | ||||||
| chr2:241460071
|
A | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0022a0001c0003t0001g0023others(2): Show | 5 | NA18949.hp2 NA18951.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-2452A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460071 | ||||||
| chr2:241460078
|
C | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(82): Show | 85 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1588-2445C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460078 | ||||||
| chr2:241460103
|
C | G | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1588-2420C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460103 | ||||||
| chr2:241460286
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0109 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1588-2237G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460286 | ||||||
| chr2:241460312
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1588-2211G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460312 | ||||||
| chr2:241460447
|
C | CT | 32 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-2064dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241460447 | |||||
| chr2:241460448
|
T | G | 88 | a0001c0001t0001g0136a0001c0001t0001g0205a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1588-2075T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460448 | ||||||
| chr2:241460511
|
C | T | 1 | a0001c0001t0009g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1588-2012C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460511 | ||||||
| chr2:241460512
|
G | A | 120 | a0001c0001t0001g0136a0001c0001t0001g0205a0001c0001t0001g0206others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1588-2011G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460512 | ||||||
| chr2:241460606
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1588-1917T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460606 | ||||||
| chr2:241460685
|
A | AG | 91 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1588-1837dupG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241460685 | |||||
| chr2:241460846
|
A | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1588-1677A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460846 | ||||||
| chr2:241460858
|
C | T | 3 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0357 | 3 | HG00639.hp1 HG01175.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1588-1665C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460858 | ||||||
| chr2:241460875
|
C | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1648C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460875 | ||||||
| chr2:241460876
|
G | C | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1588-1647G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460876 | ||||||
| chr2:241460891
|
C | G | 1 | a0001c0006t0001g0250 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1588-1632C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460891 | ||||||
| chr2:241460968
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1555A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241460968 | ||||||
| chr2:241461066
|
G | C | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1588-1457G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461066 | ||||||
| chr2:241461182
|
A | G | 63 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1588-1341A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461182 | ||||||
| chr2:241461211
|
C | T | 1 | a0002c0002t0006g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1588-1312C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461211 | ||||||
| chr2:241461238
|
G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1588-1285G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461238 | ||||||
| chr2:241461265
|
A | G | 1 | a0001c0003t0001g0025 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1588-1258A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461265 | ||||||
| chr2:241461308
|
G | A | 88 | a0001c0001t0001g0136a0001c0001t0001g0205a0001c0001t0001g0206others(85): Show | 88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1588-1215G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461308 | ||||||
| chr2:241461330
|
C | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1588-1193C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461330 | ||||||
| chr2:241461333
|
CCT | C | 37 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1588-1185_1588-118 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241461333 | |||||
| chr2:241461421
|
C | A | 2 | a0001c0001t0002g0373a0001c0001t0002g0375 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1588-1102C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461421 | ||||||
| chr2:241461422
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-1101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461422 | ||||||
| chr2:241461432
|
TC | T | 11 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(8): Show | 11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588-1087delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 241461432 | |||||
| chr2:241461538
|
G | A | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1588-985G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461538 | ||||||
| chr2:241461587
|
T | C | 122 | a0001c0001t0001g0136a0001c0001t0001g0158a0001c0001t0001g0205others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1588-936T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461587 | ||||||
| chr2:241461630
|
G | C | 2 | a0002c0002t0001g0338a0002c0002t0001g0343 | 2 | NA18988.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1588-893G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461630 | ||||||
| chr2:241461722
|
A | G | 1 | a0001c0003t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1588-801A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461722 | ||||||
| chr2:241461751
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1588-772C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241461751 | ||||||
| chr2:241462007
|
C | T | 91 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1588-516C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462007 | ||||||
| chr2:241462024
|
C | A | 32 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(29): Show | 32 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.1588-499C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462024 | ||||||
| chr2:241462024
|
C | G | 31 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1588-499C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462024 | ||||||
| chr2:241462070
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1588-453G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462070 | ||||||
| chr2:241462078
|
T | G | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1588-445T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462078 | ||||||
| chr2:241462138
|
G | A | 2 | a0004c0007t0001g0101a0004c0007t0001g0102 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1588-385G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462138 | ||||||
| chr2:241462144
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1588-379G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462144 | ||||||
| chr2:241462238
|
A | G | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1588-285A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462238 | ||||||
| chr2:241462292
|
C | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1588-231C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462292 | ||||||
| chr2:241462417
|
G | A | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1588-106G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | chr2 | 241462417 | ||||||
| chr2:241462646
|
T | A | 31 | a0001c0001t0001g0376a0001c0004t0001g0143a0001c0004t0001g0157others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1677+34T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462646 | ||||||
| chr2:241462647
|
A | T | 89 | a0001c0001t0001g0136a0001c0001t0001g0205a0001c0001t0001g0206others(86): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1677+35A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462647 | ||||||
| chr2:241462672
|
G | C | 29 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1677+60G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462672 | ||||||
| chr2:241462745
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1677+133G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241462745 | ||||||
| chr2:241463048
|
C | G | 21 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1678-287C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463048 | ||||||
| chr2:241463178
|
A | C | 1 | a0002c0002t0001g0340 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1678-157A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463178 | ||||||
| chr2:241463255
|
T | G | 1 | a0001c0003t0001g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1678-80T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | chr2 | 241463255 | ||||||
| chr2:241463262
|
AG | A | 3 | a0002c0002t0001g0200a0002c0002t0001g0354a0002c0002t0001g0358 | 3 | NA18960.hp1 NA18972.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1678-71delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 241463262 | |||||
| chr2:241463488
|
C | G | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1811+20C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463488 | ||||||
| chr2:241463523
|
G | A | 1 | a0001c0003t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1811+55G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463523 | ||||||
| chr2:241463665
|
G | T | 1 | a0004c0007t0001g0100 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1811+197G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463665 | ||||||
| chr2:241463704
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1812-195A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 16/26 | chr2 | 241463704 | ||||||
| chr2:241464083
|
G | GTCCCCTC others(9): Show |
2 | a0003c0005t0001g0044a0003c0005t0001g0045 | 2 | NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1893+109_1893+124d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464083 | |||||
| chr2:241464215
|
C | T | 1 | a0001c0001t0001g0376 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1893+235C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464215 | ||||||
| chr2:241464247
|
CTCCTCAA others(42): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1893+279_1893+327d others(51): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464247 | |||||
| chr2:241464355
|
G | A | 1 | a0001c0004t0001g0175 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1893+375G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464355 | ||||||
| chr2:241464369
|
A | AGAGGGAC others(10): Show |
1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1893+389_1893+390i others(19): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464369 | ||||||
| chr2:241464480
|
C | T | 1 | a0002c0002t0001g0357 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1893+500C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464480 | ||||||
| chr2:241464506
|
T | A | 156 | a0001c0001t0001g0158a0001c0001t0001g0205a0001c0001t0001g0206others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1893+526T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464506 | ||||||
| chr2:241464516
|
A | AAGCAGGG others(9): Show |
69 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1893+544_1893+545i others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464516 | |||||
| chr2:241464525
|
T | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(176): Show | 179 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1893+545T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464525 | ||||||
| chr2:241464588
|
G | T | 39 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(36): Show | 39 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1893+608G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464588 | ||||||
| chr2:241464591
|
CTCTCAGA others(9): Show |
C | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1893+620_1893+635d others(18): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241464591 | |||||
| chr2:241464720
|
G | T | 70 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1893+740G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464720 | ||||||
| chr2:241464903
|
T | A | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1893+923T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241464903 | ||||||
| chr2:241465000
|
C | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG00639.hp2 HG03927.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1893+1020C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465000 | ||||||
| chr2:241465022
|
A | G | 31 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1893+1042A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465022 | ||||||
| chr2:241465079
|
G | A | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1893+1099G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465079 | ||||||
| chr2:241465246
|
T | C | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1893+1266T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465246 | ||||||
| chr2:241465329
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1893+1349T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465329 | ||||||
| chr2:241465353
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1893+1373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465353 | ||||||
| chr2:241465606
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1893+1626C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465606 | ||||||
| chr2:241465694
|
G | C | 1 | a0001c0001t0002g0372 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1893+1714G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465694 | ||||||
| chr2:241465737
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1893+1757G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465737 | ||||||
| chr2:241465755
|
C | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1893+1775C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241465755 | ||||||
| chr2:241466053
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1893+2073A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466053 | ||||||
| chr2:241466106
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1894-2034G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466106 | ||||||
| chr2:241466319
|
C | A | 1 | a0001c0003t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1894-1821C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466319 | ||||||
| chr2:241466357
|
G | A | 87 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(84): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1894-1783G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466357 | ||||||
| chr2:241466455
|
C | T | 1 | a0001c0004t0001g0359 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1894-1685C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466455 | ||||||
| chr2:241466640
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1894-1500C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466640 | ||||||
| chr2:241466657
|
G | A | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1894-1483G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466657 | ||||||
| chr2:241466682
|
T | C | 377 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(374): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1894-1458T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466682 | ||||||
| chr2:241466689
|
A | AC | 66 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0068others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1894-1440dupC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | |||||
| chr2:241466689
|
A | ACC | 17 | a0001c0001t0001g0130a0001c0003t0001g0007a0001c0003t0001g0009others(14): Show | 17 | HG01192.hp1 HG01243.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1894-1441_1894-144 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | |||||
| chr2:241466689
|
AC | A | 66 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0209others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1894-1440delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466689 | |||||
| chr2:241466692
|
C | T | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1894-1448C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466692 | ||||||
| chr2:241466693
|
C | G | 30 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1894-1447C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466693 | ||||||
| chr2:241466695
|
C | G | 1 | a0003c0005t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1894-1445C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466695 | ||||||
| chr2:241466696
|
C | G | 1 | a0003c0005t0001g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1894-1444C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466696 | ||||||
| chr2:241466698
|
C | A | 123 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(120): Show | 123 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.1894-1442C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466698 | ||||||
| chr2:241466698
|
C | G | 8 | a0001c0025t0001g0160a0005c0008t0001g0146a0005c0008t0001g0147others(5): Show | 8 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1894-1442C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466698 | ||||||
| chr2:241466700
|
C | T | 1 | a0001c0004t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1894-1440C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466700 | ||||||
| chr2:241466830
|
C | T | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1894-1310C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241466830 | ||||||
| chr2:241466947
|
T | TAAA | 24 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(21): Show | 24 | HG00544.hp2 HG00639.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1894-1181_1894-117 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241466947 | |||||
| chr2:241467131
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1894-1009T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467131 | ||||||
| chr2:241467149
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1894-991G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467149 | ||||||
| chr2:241467210
|
C | T | 1 | a0007c0013t0001g0028 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1894-930C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467210 | ||||||
| chr2:241467239
|
G | C | 29 | a0001c0001t0001g0098a0001c0001t0001g0205a0001c0001t0001g0206others(26): Show | 29 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1894-901G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467239 | ||||||
| chr2:241467455
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1894-685G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467455 | ||||||
| chr2:241467495
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1894-645A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467495 | ||||||
| chr2:241467566
|
C | T | 38 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1894-574C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467566 | ||||||
| chr2:241467581
|
G | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1894-559G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467581 | ||||||
| chr2:241467641
|
C | CA | 40 | a0001c0001t0001g0086a0001c0001t0001g0158a0001c0001t0001g0205others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1894-482dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241467641 | |||||
| chr2:241467641
|
CA | C | 11 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0136others(8): Show | 11 | HG02965.hp1 HG03491.hp1 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1894-482delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr2 | 241467641 | |||||
| chr2:241467764
|
G | A | 35 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1894-376G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467764 | ||||||
| chr2:241467812
|
C | T | 59 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(56): Show | 59 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1894-328C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241467812 | ||||||
| chr2:241468052
|
C | T | 37 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1894-88C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241468052 | ||||||
| chr2:241468063
|
A | G | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1894-77A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 17/26 | chr2 | 241468063 | ||||||
| chr2:241468470
|
G | A | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2131+93G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468470 | ||||||
| chr2:241468475
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2131+98C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468475 | ||||||
| chr2:241468547
|
C | G | 1 | a0001c0006t0001g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2131+170C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468547 | ||||||
| chr2:241468804
|
G | A | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2131+427G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468804 | ||||||
| chr2:241468942
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2131+565A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241468942 | ||||||
| chr2:241469092
|
G | GT | 37 | a0001c0001t0001g0142a0001c0001t0001g0205a0001c0001t0001g0206others(34): Show | 37 | HG00423.hp2 HG00639.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.2131+726dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241469092 | |||||
| chr2:241469309
|
A | G | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2131+932A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469309 | ||||||
| chr2:241469533
|
C | T | 7 | a0001c0004t0001g0161a0001c0004t0001g0162a0001c0004t0001g0163others(4): Show | 7 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2131+1156C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469533 | ||||||
| chr2:241469566
|
T | C | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2131+1189T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469566 | ||||||
| chr2:241469912
|
C | T | 2 | a0001c0001t0002g0373a0001c0001t0002g0375 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2131+1535C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241469912 | ||||||
| chr2:241470068
|
C | G | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2131+1691C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470068 | ||||||
| chr2:241470145
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2131+1768C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470145 | ||||||
| chr2:241470286
|
A | G | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2131+1909A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470286 | ||||||
| chr2:241470480
|
A | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+2103A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470480 | ||||||
| chr2:241470518
|
A | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+2141A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470518 | ||||||
| chr2:241470522
|
G | C | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2131+2145G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470522 | ||||||
| chr2:241470603
|
C | T | 29 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+2226C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470603 | ||||||
| chr2:241470666
|
T | C | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+2289T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470666 | ||||||
| chr2:241470708
|
AG | A | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2131+2335delG | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241470708 | |||||
| chr2:241470710
|
G | C | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2131+2333G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470710 | ||||||
| chr2:241470746
|
G | C | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2131+2369G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470746 | ||||||
| chr2:241470842
|
CAGG | C | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+2466_2131+246 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470842 | ||||||
| chr2:241470913
|
C | G | 1 | a0001c0001t0001g0331 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2131+2536C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470913 | ||||||
| chr2:241470998
|
A | T | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2131+2621A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241470998 | ||||||
| chr2:241471006
|
C | G | 92 | a0001c0003t0001g0026a0001c0004t0001g0143a0001c0004t0001g0157others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.2131+2629C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471006 | ||||||
| chr2:241471120
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2131+2743T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471120 | ||||||
| chr2:241471161
|
G | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2131+2784G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471161 | ||||||
| chr2:241471203
|
T | C | 1 | a0002c0002t0001g0254 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2131+2826T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471203 | ||||||
| chr2:241471206
|
C | T | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2131+2829C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471206 | ||||||
| chr2:241471248
|
G | T | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2131+2871G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471248 | ||||||
| chr2:241471295
|
G | A | 1 | a0008c0021t0003g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2131+2918G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471295 | ||||||
| chr2:241471343
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2131+2966C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471343 | ||||||
| chr2:241471365
|
C | G | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2131+2988C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471365 | ||||||
| chr2:241471369
|
G | A | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+2992G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471369 | ||||||
| chr2:241471459
|
T | C | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2131+3082T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471459 | ||||||
| chr2:241471483
|
C | CT | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0063others(112): Show | 115 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.2131+3130dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | |||||
| chr2:241471483
|
C | CTT | 105 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0071others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.2131+3129_2131+313 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | |||||
| chr2:241471483
|
C | CTTT | 34 | a0001c0001t0001g0089a0001c0001t0001g0205a0001c0001t0001g0206others(31): Show | 34 | HG00423.hp2 HG00544.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2131+3128_2131+313 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | |||||
| chr2:241471483
|
CT | C | 12 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0025t0001g0160others(9): Show | 12 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2131+3130delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471483 | |||||
| chr2:241471506
|
T | G | 2 | a0001c0006t0001g0236a0001c0006t0001g0248 | 2 | NA18984.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2131+3129T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471506 | ||||||
| chr2:241471506
|
T | TG | 12 | a0001c0001t0001g0142a0001c0003t0001g0026a0001c0006t0001g0240others(9): Show | 12 | HG00408.hp1 HG00621.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2131+3129_2131+313 others(5): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471506 | ||||||
| chr2:241471533
|
A | G | 72 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0205others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.2131+3156A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471533 | ||||||
| chr2:241471556
|
G | C | 1 | a0003c0005t0001g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2131+3179G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471556 | ||||||
| chr2:241471563
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2131+3186G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471563 | ||||||
| chr2:241471584
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2131+3207C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471584 | ||||||
| chr2:241471618
|
C | T | 26 | a0001c0004t0001g0157a0001c0004t0001g0159a0001c0004t0001g0161others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.2131+3241C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471618 | ||||||
| chr2:241471642
|
C | T | 31 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2131+3265C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471642 | ||||||
| chr2:241471654
|
T | C | 151 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2131+3277T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471654 | ||||||
| chr2:241471656
|
T | G | 151 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2131+3279T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471656 | ||||||
| chr2:241471742
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2131+3365G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471742 | ||||||
| chr2:241471775
|
A | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+3398A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471775 | ||||||
| chr2:241471795
|
G | A | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3418G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471795 | ||||||
| chr2:241471902
|
G | GTTCTGTG others(187): Show |
70 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.2131+3550_2131+355 others(198): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471902 | |||||
| chr2:241471902
|
G | GTTCTGTG others(187): Show |
50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3537_2131+353 others(198): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241471902 | |||||
| chr2:241471992
|
A | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2131+3615A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241471992 | ||||||
| chr2:241472027
|
C | T | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3650C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472027 | ||||||
| chr2:241472101
|
G | A | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2131+3724G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472101 | ||||||
| chr2:241472132
|
T | C | 6 | a0001c0025t0001g0160a0005c0008t0001g0146a0005c0008t0001g0147others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2132-3725T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472132 | ||||||
| chr2:241472141
|
C | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-3716C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472141 | ||||||
| chr2:241472142
|
C | G | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-3715C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472142 | ||||||
| chr2:241472363
|
A | C | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2132-3494A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472363 | ||||||
| chr2:241472387
|
G | A | 9 | a0001c0025t0001g0160a0005c0008t0001g0144a0005c0008t0001g0146others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-3470G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472387 | ||||||
| chr2:241472412
|
T | C | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-3445T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472412 | ||||||
| chr2:241472421
|
G | A | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2132-3436G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472421 | ||||||
| chr2:241472460
|
G | C | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2132-3397G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472460 | ||||||
| chr2:241472574
|
G | A | 1 | a0001c0001t0002g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2132-3283G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472574 | ||||||
| chr2:241472663
|
C | T | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-3194C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472663 | ||||||
| chr2:241472694
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0158a0001c0001t0001g0205others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2132-3163T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472694 | ||||||
| chr2:241472785
|
A | G | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2132-3072A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472785 | ||||||
| chr2:241472851
|
G | A | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2132-3006G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472851 | ||||||
| chr2:241472943
|
A | C | 87 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(84): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2132-2914A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241472943 | ||||||
| chr2:241473257
|
A | G | 38 | a0001c0001t0001g0158a0001c0003t0001g0007a0001c0003t0001g0009others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2132-2600A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473257 | ||||||
| chr2:241473480
|
G | T | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-2377G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473480 | ||||||
| chr2:241473505
|
C | T | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2132-2352C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473505 | ||||||
| chr2:241473560
|
G | C | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2132-2297G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473560 | ||||||
| chr2:241473858
|
C | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-1999C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473858 | ||||||
| chr2:241473888
|
A | G | 1 | a0003c0005t0001g0008 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2132-1969A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241473888 | ||||||
| chr2:241474034
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2132-1823C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474034 | ||||||
| chr2:241474238
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2132-1619G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474238 | ||||||
| chr2:241474305
|
G | A | 1 | a0001c0006t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2132-1552G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474305 | ||||||
| chr2:241474317
|
C | CA | 12 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0131others(9): Show | 12 | HG00544.hp1 HG00741.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2132-1507dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CA | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0098others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-1507delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAA | C | 19 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0158others(16): Show | 19 | HG01106.hp1 HG01934.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2132-1508_2132-150 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAA | C | 91 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0068others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2132-1509_2132-150 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAA | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2132-1510_2132-150 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAA | C | 47 | a0001c0001t0001g0142a0001c0001t0001g0262a0001c0001t0001g0263others(44): Show | 47 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2132-1511_2132-150 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAA | C | 6 | a0001c0004t0001g0359a0001c0004t0001g0370a0001c0006t0001g0236others(3): Show | 6 | HG00609.hp2 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2132-1512_2132-150 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAAA others(1): Show |
C | 30 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.2132-1514_2132-150 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2132-1517_2132-150 others(15): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0004t0001g0360 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2132-1523_2132-150 others(21): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2132-1525_2132-150 others(23): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474317
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2132-1526_2132-150 others(24): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474317 | |||||
| chr2:241474493
|
A | C | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2132-1364A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474493 | ||||||
| chr2:241474528
|
C | T | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2132-1329C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474528 | ||||||
| chr2:241474676
|
C | T | 4 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0004t0001g0171others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.2132-1181C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474676 | ||||||
| chr2:241474801
|
T | TA | 15 | a0001c0001t0001g0378a0001c0003t0001g0026a0001c0006t0001g0236others(12): Show | 15 | HG00621.hp2 HG01192.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2132-1054dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474801
|
T | TAAATA | 34 | a0001c0006t0001g0244a0002c0002t0001g0200a0002c0002t0001g0253others(31): Show | 34 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.2132-1054_2132-105 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474801
|
T | TAATA | 112 | a0001c0001t0001g0004a0001c0001t0001g0067a0001c0001t0001g0071others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2132-1021_2132-101 others(8): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474801
|
T | TAATAAAT others(1): Show |
69 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(66): Show | 69 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2132-1025_2132-101 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474801
|
TAATAAAT others(5): Show |
T | 36 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(33): Show | 36 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2132-1029_2132-101 others(16): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474801
|
TAATAAAT others(9): Show |
T | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2132-1033_2132-101 others(20): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 241474801 | |||||
| chr2:241474807
|
A | T | 1 | a0001c0003t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2132-1050A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474807 | ||||||
| chr2:241474944
|
C | T | 1 | a0001c0004t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2132-913C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241474944 | ||||||
| chr2:241475116
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2132-741A>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475116 | ||||||
| chr2:241475247
|
T | C | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2132-610T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475247 | ||||||
| chr2:241475381
|
T | A | 3 | a0005c0008t0001g0144a0005c0008t0001g0148a0005c0008t0001g0154 | 3 | HG02647.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2132-476T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475381 | ||||||
| chr2:241475411
|
G | A | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2132-446G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475411 | ||||||
| chr2:241475426
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0204 | 3 | HG03669.hp1 HG03704.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2132-431C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475426 | ||||||
| chr2:241475459
|
C | T | 31 | a0003c0005t0001g0008a0003c0005t0001g0039a0003c0005t0001g0040others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2132-398C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475459 | ||||||
| chr2:241475671
|
T | C | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2132-186T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 18/26 | chr2 | 241475671 | ||||||
| chr2:241476061
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2262+74A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476061 | ||||||
| chr2:241476108
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2262+121C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476108 | ||||||
| chr2:241476202
|
A | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2262+215A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476202 | ||||||
| chr2:241476214
|
TA | T | 141 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0076others(138): Show | 141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2262+248delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241476214 | |||||
| chr2:241476214
|
TAA | T | 7 | a0001c0001t0001g0225a0001c0001t0001g0377a0001c0003t0001g0010others(4): Show | 7 | HG01167.hp2 HG01256.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2262+247_2262+248d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241476214 | |||||
| chr2:241476215
|
A | T | 1 | a0001c0001t0001g0327 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2262+228A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476215 | ||||||
| chr2:241476310
|
C | T | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2262+323C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476310 | ||||||
| chr2:241476323
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2262+336G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476323 | ||||||
| chr2:241476457
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2262+470G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476457 | ||||||
| chr2:241476517
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2262+530G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476517 | ||||||
| chr2:241476593
|
G | A | 4 | a0001c0004t0001g0143a0001c0004t0001g0360a0001c0004t0001g0361others(1): Show | 4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2262+606G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476593 | ||||||
| chr2:241476594
|
C | T | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2262+607C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476594 | ||||||
| chr2:241476946
|
G | C | 27 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0011others(24): Show | 27 | HG00609.hp1 HG01106.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.2262+959G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241476946 | ||||||
| chr2:241477004
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2262+1017T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477004 | ||||||
| chr2:241477123
|
C | CT | 17 | a0001c0001t0001g0069a0001c0001t0001g0098a0001c0001t0001g0103others(14): Show | 17 | HG01256.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2262+1157dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | |||||
| chr2:241477123
|
C | CTT | 47 | a0001c0003t0001g0026a0001c0004t0001g0359a0001c0004t0001g0361others(44): Show | 47 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2262+1156_2262+115 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | |||||
| chr2:241477123
|
C | CTTT | 51 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2262+1155_2262+115 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | |||||
| chr2:241477123
|
CT | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0158a0001c0001t0001g0233others(7): Show | 10 | HG00099.hp1 HG02129.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2262+1157delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241477123 | |||||
| chr2:241477354
|
T | A | 1 | a0020c0031t0001g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2262+1367T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477354 | ||||||
| chr2:241477502
|
C | G | 1 | a0001c0004t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2262+1515C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477502 | ||||||
| chr2:241477550
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+1563G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477550 | ||||||
| chr2:241477698
|
C | T | 1 | a0001c0025t0001g0160 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2262+1711C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477698 | ||||||
| chr2:241477770
|
T | G | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2262+1783T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477770 | ||||||
| chr2:241477904
|
T | G | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2262+1917T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241477904 | ||||||
| chr2:241478193
|
G | A | 1 | a0011c0020t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2262+2206G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478193 | ||||||
| chr2:241478393
|
C | T | 30 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2262+2406C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478393 | ||||||
| chr2:241478535
|
G | A | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2262+2548G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478535 | ||||||
| chr2:241478838
|
C | G | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2262+2851C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478838 | ||||||
| chr2:241478947
|
C | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+2960C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478947 | ||||||
| chr2:241478964
|
A | T | 1 | a0009c0012t0001g0002 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2262+2977A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241478964 | ||||||
| chr2:241479082
|
G | C | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2262+3095G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479082 | ||||||
| chr2:241479203
|
T | C | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2262+3216T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479203 | ||||||
| chr2:241479258
|
A | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0224 | 2 | HG01358.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2262+3271A>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479258 | ||||||
| chr2:241479360
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0281a0001c0001t0001g0299 | 3 | NA18949.hp1 NA18990.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2262+3373C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479360 | ||||||
| chr2:241479361
|
G | A | 2 | a0002c0002t0001g0254a0017c0017t0001g0255 | 2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2262+3374G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479361 | ||||||
| chr2:241479393
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2262+3406G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479393 | ||||||
| chr2:241479393
|
G | T | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2262+3406G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479393 | ||||||
| chr2:241479453
|
G | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2262+3466G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479453 | ||||||
| chr2:241479545
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2262+3558C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479545 | ||||||
| chr2:241479734
|
GT | G | 30 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2263-3730delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241479734 | ||||||
| chr2:241480247
|
CTCA | C | 29 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2263-3215_2263-321 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241480247 | |||||
| chr2:241480249
|
C | T | 2 | a0001c0003t0001g0038a0005c0014t0001g0149 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2263-3216C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480249 | ||||||
| chr2:241480452
|
G | A | 31 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2263-3013G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480452 | ||||||
| chr2:241480532
|
GT | G | 284 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2263-2922delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241480532 | |||||
| chr2:241480599
|
C | T | 1 | a0002c0002t0001g0256 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2263-2866C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480599 | ||||||
| chr2:241480770
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2263-2695T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480770 | ||||||
| chr2:241480979
|
G | A | 29 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(26): Show | 29 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2263-2486G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241480979 | ||||||
| chr2:241481007
|
C | G | 33 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2263-2458C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481007 | ||||||
| chr2:241481034
|
C | T | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2263-2431C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481034 | ||||||
| chr2:241481056
|
C | CA | 13 | a0001c0001t0001g0098a0001c0001t0001g0115a0001c0001t0001g0122others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2263-2384dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | |||||
| chr2:241481056
|
CA | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(162): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2263-2384delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | |||||
| chr2:241481056
|
CAA | C | 64 | a0001c0001t0001g0158a0001c0001t0001g0275a0001c0003t0001g0007others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2263-2385_2263-238 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | |||||
| chr2:241481056
|
CAAAAAAA | C | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2263-2390_2263-238 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | |||||
| chr2:241481056
|
CAAAAAAA others(3): Show |
C | 37 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2263-2393_2263-238 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241481056 | |||||
| chr2:241481556
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2263-1909G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481556 | ||||||
| chr2:241481683
|
C | T | 2 | a0001c0001t0001g0366a0001c0001t0001g0367 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2263-1782C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481683 | ||||||
| chr2:241481899
|
G | A | 87 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(84): Show | 87 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2263-1566G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241481899 | ||||||
| chr2:241482451
|
G | A | 284 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2263-1014G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482451 | ||||||
| chr2:241482457
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2263-1008C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482457 | ||||||
| chr2:241482550
|
C | T | 9 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2263-915C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482550 | ||||||
| chr2:241482676
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2263-789T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482676 | ||||||
| chr2:241482734
|
C | T | 3 | a0002c0002t0001g0200a0002c0002t0001g0354a0002c0002t0001g0358 | 3 | NA18960.hp1 NA18972.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2263-731C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482734 | ||||||
| chr2:241482969
|
TTGGTGCT others(55): Show |
T | 27 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2263-476_2263-415d others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr2 | 241482969 | |||||
| chr2:241482989
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2263-476C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482989 | ||||||
| chr2:241482989
|
CGGGAGAA others(55): Show |
C | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2263-475_2263-414d others(64): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482989 | ||||||
| chr2:241482990
|
G | A | 254 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(251): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2263-475G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241482990 | ||||||
| chr2:241483031
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2263-434C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483031 | ||||||
| chr2:241483252
|
G | A | 1 | a0001c0003t0001g0010 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2263-213G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483252 | ||||||
| chr2:241483358
|
C | T | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2263-107C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483358 | ||||||
| chr2:241483373
|
G | A | 2 | a0009c0012t0001g0001a0009c0012t0001g0002 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2263-92G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483373 | ||||||
| chr2:241483381
|
G | A | 1 | a0001c0003t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2263-84G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483381 | ||||||
| chr2:241483442
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2263-23G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 19/26 | chr2 | 241483442 | ||||||
| chr2:241483649
|
A | G | 1 | a0001c0003t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2331+116A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241483649 | ||||||
| chr2:241483672
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2331+139G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241483672 | ||||||
| chr2:241484133
|
A | G | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2332-109A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 20/26 | chr2 | 241484133 | ||||||
| chr2:241484498
|
T | A | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2421+167T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484498 | ||||||
| chr2:241484695
|
T | C | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2421+364T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484695 | ||||||
| chr2:241484729
|
G | A | 1 | a0001c0001t0004g0265 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2421+398G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484729 | ||||||
| chr2:241484762
|
TC | T | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG00642.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2421+433delC | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241484762 | |||||
| chr2:241484930
|
G | A | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2421+599G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484930 | ||||||
| chr2:241484968
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2421+637C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241484968 | ||||||
| chr2:241485272
|
A | G | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2421+941A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485272 | ||||||
| chr2:241485551
|
G | A | 1 | a0001c0004t0001g0361 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2421+1220G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485551 | ||||||
| chr2:241485638
|
C | A | 6 | a0001c0001t0002g0372a0001c0001t0002g0373a0001c0001t0002g0374others(3): Show | 6 | HG01261.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2421+1307C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485638 | ||||||
| chr2:241485819
|
G | A | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2421+1488G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485819 | ||||||
| chr2:241485822
|
C | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18961.hp2 NA19074.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2421+1491C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485822 | ||||||
| chr2:241485969
|
G | A | 1 | a0001c0015t0002g0371 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2421+1638G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485969 | ||||||
| chr2:241485977
|
C | T | 7 | a0003c0005t0001g0008a0003c0005t0001g0040a0003c0005t0001g0052others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2421+1646C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241485977 | ||||||
| chr2:241486170
|
T | G | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2421+1839T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486170 | ||||||
| chr2:241486287
|
C | CT | 118 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0206others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2421+1978dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | |||||
| chr2:241486287
|
C | CTT | 26 | a0001c0001t0001g0158a0001c0003t0001g0026a0001c0003t0001g0060others(23): Show | 26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2421+1977_2421+197 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | |||||
| chr2:241486287
|
CT | C | 12 | a0001c0001t0001g0085a0001c0001t0001g0133a0001c0001t0001g0188others(9): Show | 12 | HG00323.hp1 HG00558.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2421+1978delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486287 | |||||
| chr2:241486410
|
C | T | 11 | a0004c0007t0001g0096a0004c0007t0001g0097a0004c0007t0001g0100others(8): Show | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2421+2079C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486410 | ||||||
| chr2:241486461
|
C | CA | 12 | a0001c0001t0001g0285a0001c0001t0001g0316a0001c0001t0001g0376others(9): Show | 12 | HG00735.hp2 HG01123.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2421+2156dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | |||||
| chr2:241486461
|
CA | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0067others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2421+2156delA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | |||||
| chr2:241486461
|
CAA | C | 117 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(114): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2421+2155_2421+215 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486461 | |||||
| chr2:241486524
|
C | CATT | 323 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.2421+2193_2421+219 others(7): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486524 | ||||||
| chr2:241486602
|
G | C | 1 | a0005c0008t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2421+2271G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486602 | ||||||
| chr2:241486885
|
G | C | 11 | a0004c0007t0001g0096a0004c0007t0001g0097a0004c0007t0001g0100others(8): Show | 11 | HG01099.hp1 HG01109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2421+2554G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486885 | ||||||
| chr2:241486933
|
AAGCAGCC others(6): Show |
A | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2421+2615_2421+262 others(17): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241486933 | |||||
| chr2:241486956
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2421+2625A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486956 | ||||||
| chr2:241486984
|
G | A | 39 | a0001c0001t0001g0098a0001c0001t0001g0378a0001c0001t0002g0372others(36): Show | 39 | HG00099.hp1 HG00140.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2421+2653G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241486984 | ||||||
| chr2:241487005
|
CCT | C | 30 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2421+2675_2421+267 others(6): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487005 | ||||||
| chr2:241487012
|
C | T | 1 | a0005c0008t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2421+2681C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487012 | ||||||
| chr2:241487048
|
A | G | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2421+2717A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487048 | ||||||
| chr2:241487108
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2421+2777G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487108 | ||||||
| chr2:241487277
|
A | G | 37 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2422-2685A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487277 | ||||||
| chr2:241487529
|
G | A | 3 | a0001c0010t0001g0363a0001c0010t0001g0364a0001c0010t0001g0365 | 3 | HG00741.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2422-2433G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487529 | ||||||
| chr2:241487588
|
A | ACCTGGGA others(43): Show |
91 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.2422-2367_2422-231 others(54): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487588 | |||||
| chr2:241487666
|
C | CA | 334 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2422-2282dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487666 | |||||
| chr2:241487746
|
C | CTTTTT | 63 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(60): Show | 63 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.2422-2199_2422-219 others(9): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487746
|
C | CTTTTTT | 51 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0212others(48): Show | 51 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2422-2200_2422-219 others(10): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487746
|
C | CTTTTTTT | 137 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2422-2201_2422-219 others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487746
|
C | CTTTTTTT others(1): Show |
57 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0081others(54): Show | 57 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.2422-2202_2422-219 others(12): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487746
|
C | CTTTTTTT others(2): Show |
13 | a0001c0001t0001g0158a0001c0001t0001g0330a0001c0003t0001g0009others(10): Show | 13 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2422-2203_2422-219 others(13): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487746
|
C | CTTTTTTT others(3): Show |
1 | a0001c0003t0001g0030 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2422-2204_2422-219 others(14): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241487746 | |||||
| chr2:241487840
|
C | G | 1 | a0001c0001t0002g0372 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2422-2122C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487840 | ||||||
| chr2:241487938
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2422-2024C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487938 | ||||||
| chr2:241487984
|
G | A | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422-1978G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241487984 | ||||||
| chr2:241488023
|
C | A | 1 | a0001c0001t0001g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2422-1939C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488023 | ||||||
| chr2:241488046
|
C | G | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2422-1916C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488046 | ||||||
| chr2:241488166
|
G | GA | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2422-1791dupA | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241488166 | |||||
| chr2:241488174
|
G | C | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2422-1788G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488174 | ||||||
| chr2:241488416
|
G | GT | 66 | a0001c0001t0001g0075a0001c0001t0001g0122a0001c0001t0001g0281others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.2422-1527dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 241488416 | |||||
| chr2:241488550
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2422-1412G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488550 | ||||||
| chr2:241488590
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2422-1372C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488590 | ||||||
| chr2:241488604
|
G | T | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-1358G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488604 | ||||||
| chr2:241488611
|
A | G | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-1351A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488611 | ||||||
| chr2:241488638
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2422-1324G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488638 | ||||||
| chr2:241488642
|
C | T | 5 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0212others(2): Show | 5 | HG00423.hp2 HG02135.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2422-1320C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488642 | ||||||
| chr2:241488646
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2422-1316C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488646 | ||||||
| chr2:241488679
|
T | C | 34 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2422-1283T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488679 | ||||||
| chr2:241488691
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2422-1271T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488691 | ||||||
| chr2:241488701
|
A | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0231others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.2422-1261A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488701 | ||||||
| chr2:241488968
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0093 | 2 | HG03491.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2422-994C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241488968 | ||||||
| chr2:241489098
|
A | G | 28 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(25): Show | 28 | HG00280.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.2422-864A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489098 | ||||||
| chr2:241489171
|
G | C | 50 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(47): Show | 50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2422-791G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489171 | ||||||
| chr2:241489305
|
T | C | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422-657T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489305 | ||||||
| chr2:241489387
|
A | G | 1 | a0001c0004t0001g0370 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2422-575A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489387 | ||||||
| chr2:241489394
|
G | T | 120 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2422-568G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489394 | ||||||
| chr2:241489426
|
G | A | 1 | a0016c0030t0001g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2422-536G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489426 | ||||||
| chr2:241489495
|
G | A | 111 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2422-467G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489495 | ||||||
| chr2:241489498
|
G | A | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.2422-464G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489498 | ||||||
| chr2:241489657
|
C | T | 30 | a0001c0004t0001g0143a0001c0004t0001g0157a0001c0004t0001g0159others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2422-305C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489657 | ||||||
| chr2:241489744
|
G | C | 1 | a0006c0009t0001g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2422-218G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489744 | ||||||
| chr2:241489820
|
T | G | 3 | a0001c0004t0001g0175a0001c0004t0001g0359a0001c0004t0001g0370 | 3 | HG02257.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2422-142T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 21/26 | chr2 | 241489820 | ||||||
| chr2:241490077
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2504+33C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490077 | ||||||
| chr2:241490112
|
G | A | 1 | a0013c0024t0001g0087 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2504+68G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490112 | ||||||
| chr2:241490217
|
G | A | 14 | a0001c0003t0001g0026a0001c0006t0001g0236a0001c0006t0001g0240others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2504+173G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490217 | ||||||
| chr2:241490392
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2504+348G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490392 | ||||||
| chr2:241490443
|
CCCAGCCC others(2): Show |
C | 92 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0201others(89): Show | 92 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.2504+403_2504+411d others(11): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 241490443 | |||||
| chr2:241490550
|
A | G | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2504+506A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490550 | ||||||
| chr2:241490658
|
C | T | 1 | a0015c0029t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2505-403C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490658 | ||||||
| chr2:241490669
|
C | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2505-392C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490669 | ||||||
| chr2:241490670
|
C | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(122): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2505-391C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490670 | ||||||
| chr2:241490755
|
C | T | 78 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.2505-306C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490755 | ||||||
| chr2:241490830
|
C | G | 37 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2505-231C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490830 | ||||||
| chr2:241490911
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2505-150G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 22/26 | chr2 | 241490911 | ||||||
| chr2:241491205
|
G | C | 1 | a0003c0005t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2623+26G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491205 | ||||||
| chr2:241491306
|
T | G | 2 | a0001c0003t0001g0016a0001c0003t0001g0017 | 2 | HG00609.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2623+127T>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491306 | ||||||
| chr2:241491324
|
C | A | 9 | a0003c0005t0001g0190a0003c0005t0001g0192a0003c0005t0001g0193others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+145C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 23/26 | chr2 | 241491324 | ||||||
| chr2:241491746
|
TGAG | T | 36 | a0002c0002t0001g0200a0002c0002t0001g0253a0002c0002t0001g0254others(33): Show | 36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.2787+72_2787+74del others(3): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr2 | 241491746 | |||||
| chr2:241492030
|
C | T | 55 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(52): Show | 55 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2787+351C>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492030 | ||||||
| chr2:241492093
|
G | T | 1 | a0001c0003t0001g0026 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2787+414G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492093 | ||||||
| chr2:241492170
|
C | G | 29 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(26): Show | 29 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2787+491C>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492170 | ||||||
| chr2:241492409
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2788-520G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492409 | ||||||
| chr2:241492534
|
G | T | 1 | a0001c0001t0001g0378 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2788-395G>T | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492534 | ||||||
| chr2:241492575
|
C | A | 38 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0010others(35): Show | 38 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2788-354C>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492575 | ||||||
| chr2:241492696
|
T | C | 1 | a0007c0013t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2788-233T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492696 | ||||||
| chr2:241492727
|
T | C | 28 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2788-202T>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 24/26 | chr2 | 241492727 | ||||||
| chr2:241493115
|
G | GTATT | 4 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0042others(1): Show | 4 | HG03239.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2895+81_2895+84dup others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr2 | 241493115 | |||||
| chr2:241493192
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2896-101G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493192 | ||||||
| chr2:241493214
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2896-79G>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493214 | ||||||
| chr2:241493289
|
G | C | 111 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
splice_region_variant&intron_variant | LOW | c.2896-4G>C | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 25/26 | chr2 | 241493289 | ||||||
| chr2:241493597
|
G | GT | 90 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0142others(87): Show | 90 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.3047+167dupT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | |||||
| chr2:241493597
|
G | GTT | 8 | a0001c0001t0001g0263a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG01255.hp1 HG02976.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.3047+166_3047+167d others(4): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | |||||
| chr2:241493597
|
GT | G | 107 | a0001c0001t0001g0137a0001c0001t0001g0205a0001c0001t0001g0206others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3047+167delT | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 241493597 | |||||
| chr2:241493655
|
T | A | 1 | a0001c0003t0001g0020 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3047+211T>A | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | chr2 | 241493655 | ||||||
| chr2:241493933
|
A | G | 325 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0064others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3048-75A>G | FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 26/26 | chr2 | 241493933 |