Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 89846 |
|---|---|
| ensemblid | ENSG00000127084.19 |
| hgncid | 16027 |
| symbol | FGD3 |
| name | FYVE, RhoGEF and PH domain containing 3 |
| refseq_nuc | NM_001083536.2 |
| refseq_prot | NP_001077005.1 |
| ensembl_nuc | ENST00000375482.8 |
| ensembl_prot | ENSP00000364631.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 92947523 |
| end | 93036233 |
| strand | + |
| ver | v1.2 |
| region | chr9:92947523-93036233 |
| region5000 | chr9:92942523-93041233 |
| regionname0 | FGD3_chr9_92947523_93036233 |
| regionname5000 | FGD3_chr9_92942523_93041233 |
| 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 | 725 | 283 | 75 | 49 | 109 | 12 | 36 | 83 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002 | 0/0 | 725 | 33 | 0 | 12 | 21 | 0 | 0 | 11 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0003 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0004 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0005 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0006 | 0/0 | 725 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0007 | 0/0 | 725 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0008 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2178 | 124 | 21 | 17 | 57 | 6 | 22 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0002 | 0/0 | 2178 | 94 | 21 | 21 | 41 | 1 | 10 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0003 | 0/0 | 2178 | 28 | 0 | 12 | 16 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0004 | 0/0 | 2178 | 28 | 11 | 8 | 6 | 3 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0005 | 0/0 | 2178 | 13 | 9 | 2 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0006 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0007 | 0/0 | 2178 | 3 | 0 | 0 | 3 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0008 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0009 | 0/0 | 2178 | 2 | 0 | 0 | 0 | 0 | 2 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0010 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0011 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0012 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0013 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0014 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0015 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0016 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0017 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0018 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0019 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0020 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0021 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0022 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0023 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0024 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0025 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0026 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0027 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0028 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0029 | 1/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0030 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| c0031 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1069 | 117 | 23 | 30 | 46 | 7 | 11 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0002 | 1/0 | 1069 | 65 | 9 | 16 | 30 | 0 | 9 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0003 | 0/1 | 1069 | 43 | 4 | 4 | 19 | 4 | 11 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0004 | 0/0 | 1069 | 43 | 27 | 7 | 7 | 1 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0005 | 0/0 | 1069 | 21 | 0 | 2 | 16 | 0 | 3 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0006 | 0/0 | 1069 | 12 | 0 | 0 | 12 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0007 | 0/0 | 1069 | 5 | 5 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0008 | 0/0 | 1069 | 3 | 0 | 1 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0009 | 0/0 | 1069 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0010 | 0/0 | 1069 | 2 | 0 | 2 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0011 | 0/0 | 1069 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0012 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0013 | 0/0 | 1069 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0014 | 0/0 | 1069 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0015 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0016 | 0/0 | 1069 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0017 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| t0018 | 0/0 | 1069 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| 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 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2178 | 124 | 21 | 17 | 57 | 6 | 22 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0002 | 0/0 | 2178 | 94 | 21 | 21 | 41 | 1 | 10 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004 | 0/0 | 2178 | 28 | 11 | 8 | 6 | 3 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0005 | 0/0 | 2178 | 13 | 9 | 2 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0006 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0008 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0009 | 0/0 | 2178 | 2 | 0 | 0 | 0 | 0 | 2 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0010 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0011 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0012 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0014 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0015 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0016 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0017 | 0/0 | 2178 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0018 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0020 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0021 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0023 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0029 | 1/0 | 2178 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0030 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0031 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0003 | 0/0 | 2178 | 28 | 0 | 12 | 16 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0007 | 0/0 | 2178 | 3 | 0 | 0 | 3 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0013 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0027 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0003c0026 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0004c0019 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0005c0028 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0006c0022 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0007c0024 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0008c0025 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3246 | 60 | 9 | 12 | 24 | 4 | 11 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0003 | 0/1 | 3246 | 33 | 3 | 2 | 18 | 2 | 7 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0005 | 0/0 | 3246 | 18 | 0 | 2 | 13 | 0 | 3 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0007 | 0/0 | 3246 | 5 | 5 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0008 | 0/0 | 3246 | 2 | 0 | 1 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0009 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0011 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0013 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0001t0016 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0002t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0002t0002 | 0/0 | 3246 | 58 | 8 | 15 | 26 | 0 | 9 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0002t0004 | 0/0 | 3246 | 23 | 13 | 6 | 2 | 1 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0002t0006 | 0/0 | 3246 | 12 | 0 | 0 | 12 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004t0001 | 0/0 | 3246 | 21 | 10 | 4 | 4 | 3 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004t0003 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004t0005 | 0/0 | 3246 | 2 | 0 | 0 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004t0010 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0004t0012 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0005t0002 | 0/0 | 3246 | 2 | 0 | 1 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0005t0004 | 0/0 | 3246 | 11 | 9 | 1 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0006t0001 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0008t0004 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0009t0003 | 0/0 | 3246 | 2 | 0 | 0 | 0 | 0 | 2 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0010t0004 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0011t0002 | 0/0 | 3246 | 2 | 0 | 0 | 2 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0012t0003 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0014t0003 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0015t0003 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0016t0003 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0017t0003 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0018t0014 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0020t0001 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0021t0018 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0023t0015 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0029t0002 | 1/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0030t0017 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0001c0031t0002 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0003t0001 | 0/0 | 3246 | 26 | 0 | 12 | 14 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0003t0003 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0003t0005 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0007t0004 | 0/0 | 3246 | 3 | 0 | 0 | 3 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0013t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0002c0027t0004 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0003c0026t0008 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0004c0019t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0005c0028t0002 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0006c0022t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0007c0024t0001 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| a0008c0025t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | copy fasta | chr9 | 92942523 | 93041233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0011g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0001t0016g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0002t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0010g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0004t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0005t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0008t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0008t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0008t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0009t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0009t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0010t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0010t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0011t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0012t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0014t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0015t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0016t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0017t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0018t0014g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0020t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0021t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0023t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0029t0002g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0030t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0001c0031t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0007t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0007t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0007t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0013t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0002c0027t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0003c0026t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0004c0019t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0005c0028t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0006c0022t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0007c0024t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| a0008c0025t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0306 | EUR | GBR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | GBR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00140 | hp1 | a0001 | c0017 | t0003 | g0047 | EUR | GBR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0287 | EUR | FIN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0025 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0026 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0225 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00544 | hp1 | a0001 | c0005 | t0004 | g0240 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00558 | hp1 | a0001 | c0002 | t0006 | g0010 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00621 | hp2 | a0002 | c0007 | t0004 | g0237 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0065 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00673 | hp1 | a0001 | c0018 | t0014 | g0305 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00673 | hp2 | a0001 | c0002 | t0006 | g0020 | EAS | CHS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00735 | hp2 | a0001 | c0004 | t0003 | g0055 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0074 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01069 | hp2 | a0001 | c0005 | t0002 | g0197 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0201 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0107 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01074 | hp1 | a0007 | c0024 | t0001 | g0063 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0164 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01081 | hp2 | a0001 | c0005 | t0004 | g0006 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0213 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0095 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0118 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0078 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01169 | hp1 | a0001 | c0002 | t0004 | g0116 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0195 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0112 | AMR | PUR | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0261 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0262 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0075 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01261 | hp1 | a0001 | c0004 | t0010 | g0067 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0254 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0056 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01361 | hp2 | a0001 | c0004 | t0003 | g0070 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0083 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0114 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01515 | hp2 | a0001 | c0015 | t0003 | g0048 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0119 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0068 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0069 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01884 | hp1 | a0001 | c0005 | t0004 | g0122 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0082 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01891 | hp2 | a0001 | c0008 | t0004 | g0003 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01943 | hp2 | a0001 | c0020 | t0001 | g0045 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01952 | hp2 | a0001 | c0002 | t0004 | g0153 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0103 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01975 | hp2 | a0001 | c0004 | t0010 | g0062 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0105 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02071 | hp1 | a0001 | c0002 | t0006 | g0017 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02074 | hp1 | a0001 | c0002 | t0006 | g0022 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0073 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02145 | hp1 | a0001 | c0016 | t0003 | g0171 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0311 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | CDX | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | CDX | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02165 | hp1 | a0002 | c0003 | t0005 | g0043 | EAS | CDX | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | CDX | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02258 | hp1 | a0001 | c0023 | t0015 | g0058 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0120 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0101 | AMR | PEL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | KHV | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0318 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0163 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0098 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02630 | hp1 | a0001 | c0005 | t0004 | g0155 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0085 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0177 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0260 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02698 | hp1 | a0001 | c0001 | t0013 | g0030 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02723 | hp2 | a0008 | c0025 | t0001 | g0150 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0206 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02809 | hp1 | a0001 | c0008 | t0004 | g0219 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0159 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02886 | hp2 | a0001 | c0005 | t0004 | g0157 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0161 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0115 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02922 | hp2 | a0001 | c0010 | t0004 | g0182 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0051 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02965 | hp2 | a0001 | c0008 | t0004 | g0002 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02970 | hp1 | a0001 | c0005 | t0004 | g0158 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02976 | hp1 | a0001 | c0031 | t0002 | g0238 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03041 | hp2 | a0001 | c0021 | t0018 | g0181 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0108 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03130 | hp1 | a0001 | c0010 | t0004 | g0183 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0113 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0121 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0096 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0154 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0111 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03225 | hp2 | a0001 | c0030 | t0017 | g0007 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0317 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0245 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03491 | hp1 | a0001 | c0009 | t0003 | g0290 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03492 | hp1 | a0001 | c0012 | t0003 | g0130 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03492 | hp2 | a0001 | c0009 | t0003 | g0289 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0315 | AFR | ESN | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0178 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0162 | AFR | GWD | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0180 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0205 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0032 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0268 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03834 | hp1 | a0001 | c0014 | t0003 | g0049 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0216 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0313 | AFR | YRI | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | YRI | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18959 | hp2 | a0001 | c0005 | t0002 | g0192 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18962 | hp1 | a0001 | c0001 | t0016 | g0167 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18969 | hp2 | a0001 | c0004 | t0005 | g0042 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18970 | hp1 | a0004 | c0019 | t0001 | g0168 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18971 | hp2 | a0001 | c0002 | t0006 | g0021 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18974 | hp1 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18974 | hp2 | a0002 | c0013 | t0001 | g0072 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0149 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18979 | hp1 | a0005 | c0028 | t0002 | g0236 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0142 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18999 | hp1 | a0001 | c0011 | t0002 | g0259 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19003 | hp1 | a0006 | c0022 | t0001 | g0220 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19010 | hp1 | a0002 | c0007 | t0004 | g0232 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19010 | hp2 | a0002 | c0003 | t0003 | g0077 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19011 | hp1 | a0002 | c0027 | t0004 | g0199 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | LWK | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19030 | hp2 | a0001 | c0006 | t0001 | g0060 | AFR | LWK | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0286 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0009 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0269 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19064 | hp1 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19078 | hp2 | a0003 | c0026 | t0008 | g0320 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19079 | hp1 | a0001 | c0002 | t0006 | g0024 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19083 | hp1 | a0001 | c0002 | t0006 | g0023 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19083 | hp2 | a0002 | c0007 | t0004 | g0231 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19084 | hp2 | a0001 | c0004 | t0005 | g0015 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19088 | hp2 | a0001 | c0011 | t0002 | g0200 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19240 | hp1 | a0001 | c0005 | t0004 | g0156 | AFR | YRI | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0239 | SAS | GIH | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0104 | AMR | CLM | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02109 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02109 | hp2 | a0001 | c0004 | t0012 | g0175 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0090 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03471 | hp1 | a0001 | c0005 | t0004 | g0179 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0312 | AFR | MSL | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | USA | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0099 | AFR | USA | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA18955 | hp2 | a0001 | c0002 | t0006 | g0027 | EAS | JPT | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0314 | AFR | USA | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | USA | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0277 | REF | REF | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| homoSapiens_grch38 | hp1 | a0001 | c0029 | t0002 | g0263 | REF | REF | FGD3_chr9_92942523_93041233 | FGD3 | chr9 | 92942523 | 93041233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:93002939
|
G | T | 1 | a0003 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.468G>T | p.Gln156His | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/18 | 892/3246 | 468/2178 | 156/725 | chr9 | 93002939 | ||
| chr9:93006100
|
A | T | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.757A>T | p.Asn253Tyr | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/18 | 1181/3246 | 757/2178 | 253/725 | chr9 | 93006100 | ||
| chr9:93006166
|
G | A | 1 | a0002 | 33 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(30): Show |
missense_variant | MODERATE | c.823G>A | p.Val275Ile | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/18 | 1247/3246 | 823/2178 | 275/725 | chr9 | 93006166 | ||
| chr9:93010369
|
C | T | 1 | a0007 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.961C>T | p.Arg321Trp | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/18 | 1385/3246 | 961/2178 | 321/725 | chr9 | 93010369 | ||
| chr9:93013916
|
C | G | 1 | a0006 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1100C>G | p.Pro367Arg | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/18 | 1524/3246 | 1100/2178 | 367/725 | chr9 | 93013916 | ||
| chr9:93013918
|
G | C | 1 | a0006 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1102G>C | p.Ala368Pro | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/18 | 1526/3246 | 1102/2178 | 368/725 | chr9 | 93013918 | ||
| chr9:93018179
|
T | A | 1 | a0005 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.1319T>A | p.Ile440Lys | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/18 | 1743/3246 | 1319/2178 | 440/725 | chr9 | 93018179 | ||
| chr9:93035345
|
G | A | 1 | a0004 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1934G>A | p.Arg645Gln | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 2358/3246 | 1934/2178 | 645/725 | chr9 | 93035345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92976499
|
C | A | 20 | a0001c0001a0001c0004a0001c0006others(17): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
synonymous_variant | LOW | c.243C>A | p.Pro81Pro | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/18 | 667/3246 | 243/2178 | 81/725 | chr9 | 92976499 | ||
| chr9:92976520
|
G | A | 1 | a0001c0012 | 1 | HG03492.hp1 | synonymous_variant | LOW | c.264G>A | p.Glu88Glu | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/18 | 688/3246 | 264/2178 | 88/725 | chr9 | 92976520 | ||
| chr9:92976643
|
C | T | 1 | a0001c0006 | 3 | HG02486.hp2 HG02965.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.387C>T | p.Asp129Asp | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/18 | 811/3246 | 387/2178 | 129/725 | chr9 | 92976643 | ||
| chr9:93010359
|
C | T | 1 | a0001c0009 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.951C>T | p.Asp317Asp | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/18 | 1375/3246 | 951/2178 | 317/725 | chr9 | 93010359 | ||
| chr9:93010384
|
A | C | 1 | a0001c0011 | 2 | NA18999.hp1 NA19088.hp2 |
splice_region_variant&synonymous_variant | LOW | c.976A>C | p.Arg326Arg | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/18 | 1400/3246 | 976/2178 | 326/725 | chr9 | 93010384 | ||
| chr9:93011239
|
C | T | 1 | a0001c0031 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1002C>T | p.Ala334Ala | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/18 | 1426/3246 | 1002/2178 | 334/725 | chr9 | 93011239 | ||
| chr9:93011245
|
C | T | 3 | a0001c0010a0001c0023a0001c0030 | 4 | HG02258.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.1008C>T | p.Asn336Asn | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/18 | 1432/3246 | 1008/2178 | 336/725 | chr9 | 93011245 | ||
| chr9:93011266
|
G | A | 1 | a0001c0014 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1029G>A | p.Arg343Arg | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/18 | 1453/3246 | 1029/2178 | 343/725 | chr9 | 93011266 | ||
| chr9:93013956
|
G | A | 1 | a0001c0015 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1140G>A | p.Leu380Leu | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/18 | 1564/3246 | 1140/2178 | 380/725 | chr9 | 93013956 | ||
| chr9:93018183
|
A | G | 30 | a0001c0001a0001c0002a0001c0004others(27): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
synonymous_variant | LOW | c.1323A>G | p.Thr441Thr | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/18 | 1747/3246 | 1323/2178 | 441/725 | chr9 | 93018183 | ||
| chr9:93020373
|
T | C | 1 | a0001c0016 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1443T>C | p.Phe481Phe | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/18 | 1867/3246 | 1443/2178 | 481/725 | chr9 | 93020373 | ||
| chr9:93020385
|
C | T | 8 | a0001c0004a0001c0005a0001c0006others(5): Show | 78 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
synonymous_variant | LOW | c.1455C>T | p.Phe485Phe | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/18 | 1879/3246 | 1455/2178 | 485/725 | chr9 | 93020385 | ||
| chr9:93022338
|
C | A | 2 | a0001c0015a0001c0017 | 2 | HG00140.hp1 HG01515.hp2 |
synonymous_variant | LOW | c.1506C>A | p.Thr502Thr | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/18 | 1930/3246 | 1506/2178 | 502/725 | chr9 | 93022338 | ||
| chr9:93034624
|
G | T | 3 | a0001c0021a0001c0023a0001c0030 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1869G>T | p.Val623Val | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/18 | 2293/3246 | 1869/2178 | 623/725 | chr9 | 93034624 | ||
| chr9:93034660
|
G | A | 1 | a0001c0018 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1905G>A | p.Leu635Leu | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/18 | 2329/3246 | 1905/2178 | 635/725 | chr9 | 93034660 | ||
| chr9:93035352
|
C | G | 1 | a0001c0008 | 3 | HG01891.hp2 HG02809.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.1941C>G | p.Pro647Pro | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 2365/3246 | 1941/2178 | 647/725 | chr9 | 93035352 | ||
| chr9:93035529
|
G | A | 1 | a0001c0020 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.2118G>A | p.Thr706Thr | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 2542/3246 | 2118/2178 | 706/725 | chr9 | 93035529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92947543
|
G | A | 1 | a0001c0004t0012 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-404G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/18 | 28714 | chr9 | 92947543 | |||||
| chr9:92947676
|
G | A | 7 | a0001c0001t0005a0001c0001t0008a0001c0001t0013others(4): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-271G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/18 | 28581 | chr9 | 92947676 | |||||
| chr9:92975256
|
A | G | 3 | a0001c0001t0007a0001c0001t0011a0001c0021t0018 | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/18 | chr9 | 92975256 | ||||||
| chr9:92975343
|
C | T | 1 | a0001c0001t0013 | 1 | HG02698.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-112C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/18 | chr9 | 92975343 | ||||||
| chr9:92975367
|
G | A | 35 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(32): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/18 | 890 | chr9 | 92975367 | |||||
| chr9:93035623
|
T | C | 1 | a0001c0001t0009 | 2 | HG03098.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*34T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 34 | chr9 | 93035623 | |||||
| chr9:93035717
|
C | T | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(23): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 128 | chr9 | 93035717 | |||||
| chr9:93035731
|
G | A | 1 | a0001c0004t0010 | 2 | HG01261.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 142 | chr9 | 93035731 | |||||
| chr9:93035831
|
G | A | 1 | a0001c0018t0014 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 242 | chr9 | 93035831 | |||||
| chr9:93035872
|
G | A | 3 | a0001c0021t0018a0001c0023t0015a0001c0030t0017 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*283G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 283 | chr9 | 93035872 | |||||
| chr9:93036080
|
C | G | 1 | a0001c0001t0016 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 18/18 | 491 | chr9 | 93036080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92947894
|
T | C | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-218+165T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92947894 | ||||||
| chr9:92948072
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-218+343G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948072 | ||||||
| chr9:92948200
|
A | ACGGGGAC others(54): Show |
1 | a0003c0026t0008g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-218+475_-218+535d others(63): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92948200 | |||||
| chr9:92948253
|
C | T | 2 | a0001c0001t0001g0321a0001c0001t0003g0322 | 2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-218+524C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948253 | ||||||
| chr9:92948340
|
G | A | 4 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218+611G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948340 | ||||||
| chr9:92948370
|
G | T | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+641G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948370 | ||||||
| chr9:92948561
|
A | G | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+832A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948561 | ||||||
| chr9:92948562
|
T | A | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+833T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948562 | ||||||
| chr9:92948703
|
A | G | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+974A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948703 | ||||||
| chr9:92948742
|
A | G | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218+1013A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948742 | ||||||
| chr9:92948829
|
G | T | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+1100G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948829 | ||||||
| chr9:92948931
|
A | G | 1 | a0001c0002t0004g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-218+1202A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92948931 | ||||||
| chr9:92949032
|
C | T | 42 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0276others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.-218+1303C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949032 | ||||||
| chr9:92949080
|
T | C | 235 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-218+1351T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949080 | ||||||
| chr9:92949221
|
A | G | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-218+1492A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949221 | ||||||
| chr9:92949362
|
T | C | 235 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-218+1633T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949362 | ||||||
| chr9:92949363
|
G | A | 4 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218+1634G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949363 | ||||||
| chr9:92949544
|
G | A | 2 | a0001c0002t0006g0009a0001c0002t0006g0010 | 2 | HG00558.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-218+1815G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949544 | ||||||
| chr9:92949583
|
C | T | 1 | a0001c0002t0004g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-218+1854C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949583 | ||||||
| chr9:92949722
|
G | A | 47 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(44): Show | 47 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-218+1993G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949722 | ||||||
| chr9:92949867
|
G | C | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+2138G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949867 | ||||||
| chr9:92949873
|
C | T | 1 | a0002c0003t0001g0114 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-218+2144C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92949873 | ||||||
| chr9:92950036
|
CT | C | 235 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-218+2318delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92950036 | |||||
| chr9:92950233
|
C | T | 1 | a0001c0001t0005g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-218+2504C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92950233 | ||||||
| chr9:92950304
|
C | CT | 10 | a0001c0001t0011g0180a0001c0002t0004g0008a0001c0002t0004g0177others(7): Show | 10 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-218+2576dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92950304 | |||||
| chr9:92950342
|
G | A | 1 | a0001c0020t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-218+2613G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92950342 | ||||||
| chr9:92950418
|
C | CA | 18 | a0001c0001t0001g0046a0001c0001t0001g0117a0001c0001t0001g0271others(15): Show | 18 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-218+2703dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92950418 | |||||
| chr9:92950599
|
A | G | 2 | a0001c0001t0001g0176a0001c0004t0012g0175 | 2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-218+2870A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92950599 | ||||||
| chr9:92950710
|
A | G | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+2981A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92950710 | ||||||
| chr9:92950803
|
G | A | 8 | a0001c0001t0001g0117a0001c0002t0002g0312a0001c0002t0004g0115others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218+3074G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92950803 | ||||||
| chr9:92951044
|
G | A | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-218+3315G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951044 | ||||||
| chr9:92951080
|
A | G | 235 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-218+3351A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951080 | ||||||
| chr9:92951104
|
G | C | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-218+3375G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951104 | ||||||
| chr9:92951126
|
A | G | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+3397A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951126 | ||||||
| chr9:92951291
|
C | A | 1 | a0001c0002t0001g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-218+3562C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951291 | ||||||
| chr9:92951378
|
C | T | 1 | a0001c0004t0001g0113 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-218+3649C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951378 | ||||||
| chr9:92951443
|
G | A | 2 | a0001c0015t0003g0048a0001c0017t0003g0047 | 2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-218+3714G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951443 | ||||||
| chr9:92951495
|
T | G | 55 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-218+3766T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951495 | ||||||
| chr9:92951569
|
G | C | 4 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(1): Show | 4 | HG00408.hp2 HG02027.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218+3840G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951569 | ||||||
| chr9:92951784
|
T | C | 1 | a0001c0014t0003g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-218+4055T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951784 | ||||||
| chr9:92951806
|
T | G | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-218+4077T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951806 | ||||||
| chr9:92951894
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-218+4165G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951894 | ||||||
| chr9:92951972
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-218+4243G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951972 | ||||||
| chr9:92951991
|
C | T | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-218+4262C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92951991 | ||||||
| chr9:92952059
|
A | G | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+4330A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952059 | ||||||
| chr9:92952112
|
A | G | 36 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(33): Show | 36 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-218+4383A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952112 | ||||||
| chr9:92952233
|
A | AT | 94 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(91): Show | 94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-218+4524dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92952233 | |||||
| chr9:92952233
|
A | ATT | 15 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0170others(12): Show | 15 | HG02027.hp1 HG02145.hp1 HG02922.hp2 others(12): Show |
intron_variant | MODIFIER | c.-218+4523_-218+452 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92952233 | |||||
| chr9:92952233
|
AT | A | 13 | a0001c0001t0005g0013a0001c0002t0002g0187a0001c0002t0002g0188others(10): Show | 13 | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-218+4524delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92952233 | |||||
| chr9:92952479
|
C | T | 1 | a0001c0002t0004g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-218+4750C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952479 | ||||||
| chr9:92952789
|
A | C | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+5060A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952789 | ||||||
| chr9:92952804
|
T | G | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-218+5075T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952804 | ||||||
| chr9:92952863
|
T | C | 317 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-218+5134T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952863 | ||||||
| chr9:92952969
|
C | T | 1 | a0001c0002t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-218+5240C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92952969 | ||||||
| chr9:92953190
|
A | G | 1 | a0001c0004t0001g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-218+5461A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953190 | ||||||
| chr9:92953195
|
C | CT | 4 | a0001c0002t0002g0184a0001c0002t0002g0257a0001c0002t0002g0258others(1): Show | 4 | NA18952.hp1 NA18998.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218+5467dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92953195 | |||||
| chr9:92953395
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-218+5666G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953395 | ||||||
| chr9:92953435
|
A | C | 172 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-218+5706A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953435 | ||||||
| chr9:92953505
|
A | T | 8 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(5): Show | 8 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218+5776A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953505 | ||||||
| chr9:92953523
|
G | A | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+5794G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953523 | ||||||
| chr9:92953770
|
T | C | 86 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(83): Show | 86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-218+6041T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92953770 | ||||||
| chr9:92954074
|
A | T | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-218+6345A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954074 | ||||||
| chr9:92954078
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-218+6349A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954078 | ||||||
| chr9:92954118
|
C | T | 1 | a0001c0002t0004g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-218+6389C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954118 | ||||||
| chr9:92954193
|
A | G | 75 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-218+6464A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954193 | ||||||
| chr9:92954395
|
C | A | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+6666C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954395 | ||||||
| chr9:92954461
|
A | T | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+6732A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954461 | ||||||
| chr9:92954466
|
C | G | 1 | a0001c0001t0003g0308 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-218+6737C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954466 | ||||||
| chr9:92954508
|
G | A | 1 | a0001c0001t0003g0309 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-218+6779G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954508 | ||||||
| chr9:92954682
|
C | G | 235 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-218+6953C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954682 | ||||||
| chr9:92954874
|
T | C | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+7145T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954874 | ||||||
| chr9:92954875
|
C | T | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+7146C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954875 | ||||||
| chr9:92954876
|
T | C | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-218+7147T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954876 | ||||||
| chr9:92954900
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-218+7171G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954900 | ||||||
| chr9:92954915
|
G | A | 52 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(49): Show | 52 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-218+7186G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92954915 | ||||||
| chr9:92955088
|
G | A | 1 | a0001c0001t0008g0012 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-218+7359G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955088 | ||||||
| chr9:92955141
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-218+7412G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955141 | ||||||
| chr9:92955148
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-218+7419G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955148 | ||||||
| chr9:92955174
|
A | T | 1 | a0001c0002t0002g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-218+7445A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955174 | ||||||
| chr9:92955309
|
C | T | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+7580C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955309 | ||||||
| chr9:92955373
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-218+7644A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955373 | ||||||
| chr9:92955426
|
C | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+7697C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955426 | ||||||
| chr9:92955532
|
A | C | 1 | a0003c0026t0008g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-218+7803A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955532 | ||||||
| chr9:92955533
|
C | T | 1 | a0003c0026t0008g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-218+7804C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955533 | ||||||
| chr9:92955547
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-218+7818A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955547 | ||||||
| chr9:92955641
|
C | A | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+7912C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955641 | ||||||
| chr9:92955809
|
C | T | 315 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-218+8080C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955809 | ||||||
| chr9:92955837
|
A | G | 1 | a0001c0002t0002g0256 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-218+8108A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955837 | ||||||
| chr9:92955893
|
A | G | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+8164A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955893 | ||||||
| chr9:92955919
|
C | T | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-218+8190C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92955919 | ||||||
| chr9:92956119
|
TTTTG | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0109a0001c0004t0001g0108 | 3 | HG02572.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-218+8414_-218+841 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92956119 | |||||
| chr9:92956146
|
T | G | 7 | a0001c0001t0001g0117a0001c0002t0004g0115a0001c0002t0004g0116others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218+8417T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956146 | ||||||
| chr9:92956334
|
G | C | 1 | a0001c0001t0003g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-218+8605G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956334 | ||||||
| chr9:92956674
|
G | A | 1 | a0001c0002t0004g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-218+8945G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956674 | ||||||
| chr9:92956742
|
G | A | 2 | a0001c0004t0001g0056a0001c0004t0003g0055 | 2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-218+9013G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956742 | ||||||
| chr9:92956782
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-218+9053C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956782 | ||||||
| chr9:92956834
|
C | CT | 70 | a0001c0001t0001g0054a0001c0001t0001g0100a0001c0001t0001g0117others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.-218+9108dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92956834 | |||||
| chr9:92956834
|
C | CTT | 45 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0005g0011others(42): Show | 45 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-218+9107_-218+910 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92956834 | |||||
| chr9:92956837
|
TC | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0321a0001c0001t0003g0124others(2): Show | 5 | HG00099.hp2 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218+9109delC | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956837 | ||||||
| chr9:92956838
|
C | T | 231 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(228): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-218+9109C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956838 | ||||||
| chr9:92956842
|
T | C | 1 | a0001c0002t0002g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-218+9113T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956842 | ||||||
| chr9:92956856
|
G | T | 45 | a0001c0001t0001g0117a0001c0001t0005g0011a0001c0001t0005g0013others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-218+9127G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956856 | ||||||
| chr9:92956930
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-218+9201C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956930 | ||||||
| chr9:92956994
|
A | G | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+9265A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92956994 | ||||||
| chr9:92957061
|
T | C | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+9332T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957061 | ||||||
| chr9:92957100
|
C | T | 1 | a0001c0001t0008g0012 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-218+9371C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957100 | ||||||
| chr9:92957158
|
A | C | 1 | a0001c0002t0002g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-218+9429A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957158 | ||||||
| chr9:92957264
|
G | C | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+9535G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957264 | ||||||
| chr9:92957448
|
G | T | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+9719G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957448 | ||||||
| chr9:92957449
|
A | T | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+9720A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957449 | ||||||
| chr9:92957481
|
C | T | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+9752C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957481 | ||||||
| chr9:92957677
|
C | CT | 8 | a0001c0001t0008g0012a0001c0002t0004g0008a0001c0002t0004g0162others(5): Show | 8 | HG01081.hp1 HG01081.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218+9967dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92957677 | |||||
| chr9:92957677
|
C | CTT | 32 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0018others(29): Show | 32 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-218+9966_-218+996 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92957677 | |||||
| chr9:92957677
|
CT | C | 175 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-218+9967delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92957677 | |||||
| chr9:92957677
|
CTT | C | 6 | a0001c0001t0001g0100a0001c0001t0001g0166a0001c0001t0003g0052others(3): Show | 6 | HG01070.hp2 HG03471.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218+9966_-218+996 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92957677 | |||||
| chr9:92957683
|
T | C | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+9954T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957683 | ||||||
| chr9:92957718
|
G | A | 4 | a0001c0001t0001g0117a0001c0002t0004g0116a0001c0002t0004g0118others(1): Show | 4 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218+9989G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957718 | ||||||
| chr9:92957756
|
A | G | 36 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(33): Show | 36 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-218+10027A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957756 | ||||||
| chr9:92957878
|
A | G | 1 | a0001c0004t0001g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-218+10149A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957878 | ||||||
| chr9:92957885
|
A | G | 236 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-218+10156A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957885 | ||||||
| chr9:92957975
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-218+10246G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92957975 | ||||||
| chr9:92958002
|
A | AT | 73 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+10287dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92958002 | |||||
| chr9:92958002
|
AT | A | 40 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-218+10287delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92958002 | |||||
| chr9:92958025
|
G | T | 1 | a0008c0025t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-218+10296G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958025 | ||||||
| chr9:92958046
|
T | C | 84 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-218+10317T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958046 | ||||||
| chr9:92958067
|
C | T | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+10338C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958067 | ||||||
| chr9:92958092
|
A | G | 236 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-218+10363A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958092 | ||||||
| chr9:92958200
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-218+10471T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958200 | ||||||
| chr9:92958330
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0251others(4): Show | 7 | HG01070.hp1 HG01167.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218+10601C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958330 | ||||||
| chr9:92958339
|
G | T | 277 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-218+10610G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958339 | ||||||
| chr9:92958436
|
T | C | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-218+10707T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958436 | ||||||
| chr9:92958583
|
A | G | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-218+10854A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958583 | ||||||
| chr9:92958595
|
T | G | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+10866T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958595 | ||||||
| chr9:92958676
|
T | C | 1 | a0001c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-218+10947T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958676 | ||||||
| chr9:92958778
|
C | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+11049C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958778 | ||||||
| chr9:92958865
|
G | A | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+11136G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958865 | ||||||
| chr9:92958873
|
GAATGAAA others(3): Show |
G | 1 | a0001c0002t0002g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218+11145_-218+11 others(16): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958873 | ||||||
| chr9:92958884
|
T | G | 1 | a0001c0002t0002g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218+11155T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958884 | ||||||
| chr9:92958888
|
A | T | 1 | a0001c0002t0002g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218+11159A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958888 | ||||||
| chr9:92958901
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218+11172C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958901 | ||||||
| chr9:92958904
|
T | A | 1 | a0001c0002t0002g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-218+11175T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92958904 | ||||||
| chr9:92959102
|
G | A | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+11373G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959102 | ||||||
| chr9:92959183
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-218+11454A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959183 | ||||||
| chr9:92959309
|
A | G | 7 | a0001c0002t0002g0184a0001c0002t0002g0249a0001c0002t0002g0250others(4): Show | 7 | NA18952.hp1 NA18970.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218+11580A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959309 | ||||||
| chr9:92959392
|
G | T | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+11663G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959392 | ||||||
| chr9:92959422
|
G | A | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+11693G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959422 | ||||||
| chr9:92959430
|
C | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+11701C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959430 | ||||||
| chr9:92959537
|
G | A | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+11808G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959537 | ||||||
| chr9:92959613
|
G | T | 8 | a0001c0001t0001g0117a0001c0002t0002g0312a0001c0002t0004g0115others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-218+11884G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959613 | ||||||
| chr9:92959622
|
C | G | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-218+11893C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959622 | ||||||
| chr9:92959625
|
C | G | 1 | a0008c0025t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-218+11896C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959625 | ||||||
| chr9:92959639
|
C | T | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-218+11910C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959639 | ||||||
| chr9:92959659
|
A | T | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-218+11930A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959659 | ||||||
| chr9:92959661
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-218+11932C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959661 | ||||||
| chr9:92959706
|
C | CA | 62 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-218+11999dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92959706 | |||||
| chr9:92959706
|
C | CAA | 143 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0057others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-218+11998_-218+11 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92959706 | |||||
| chr9:92959706
|
C | CAAA | 16 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0127others(13): Show | 16 | HG00099.hp1 HG01358.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.-218+11997_-218+11 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92959706 | |||||
| chr9:92959706
|
CA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0186a0001c0001t0001g0221others(8): Show | 11 | HG01346.hp1 HG01934.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-218+11999delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92959706 | |||||
| chr9:92959915
|
A | C | 83 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(80): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-218+12186A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959915 | ||||||
| chr9:92959940
|
G | A | 1 | a0001c0002t0004g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-218+12211G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959940 | ||||||
| chr9:92959999
|
G | A | 1 | a0001c0001t0005g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-218+12270G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92959999 | ||||||
| chr9:92960009
|
C | T | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-218+12280C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960009 | ||||||
| chr9:92960016
|
G | A | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218+12287G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960016 | ||||||
| chr9:92960131
|
T | C | 230 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-218+12402T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960131 | ||||||
| chr9:92960272
|
TCATGTCT others(1): Show |
T | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-218+12559_-218+12 others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92960272 | |||||
| chr9:92960337
|
C | T | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-218+12608C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960337 | ||||||
| chr9:92960652
|
G | A | 2 | a0001c0002t0002g0187a0001c0002t0002g0204 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-218+12923G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960652 | ||||||
| chr9:92960836
|
T | G | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-218+13107T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960836 | ||||||
| chr9:92960881
|
G | T | 61 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-218+13152G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960881 | ||||||
| chr9:92960899
|
G | A | 1 | a0001c0015t0003g0048 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-218+13170G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960899 | ||||||
| chr9:92960934
|
G | A | 1 | a0001c0010t0004g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-218+13205G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92960934 | ||||||
| chr9:92961221
|
G | A | 2 | a0001c0015t0003g0048a0001c0017t0003g0047 | 2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-218+13492G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92961221 | ||||||
| chr9:92961277
|
G | A | 1 | a0001c0004t0001g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-218+13548G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92961277 | ||||||
| chr9:92961322
|
C | T | 1 | a0001c0001t0005g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-218+13593C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92961322 | ||||||
| chr9:92961408
|
C | T | 1 | a0002c0003t0005g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-218+13679C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92961408 | ||||||
| chr9:92961552
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-217-13686G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92961552 | ||||||
| chr9:92962041
|
T | C | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-217-13197T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962041 | ||||||
| chr9:92962200
|
T | C | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-13038T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962200 | ||||||
| chr9:92962268
|
A | T | 236 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-217-12970A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962268 | ||||||
| chr9:92962367
|
C | G | 55 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(52): Show | 55 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-217-12871C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962367 | ||||||
| chr9:92962496
|
G | A | 1 | a0001c0004t0003g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-217-12742G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962496 | ||||||
| chr9:92962531
|
G | C | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-217-12707G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962531 | ||||||
| chr9:92962631
|
G | A | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-12607G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962631 | ||||||
| chr9:92962706
|
C | T | 2 | a0001c0004t0001g0068a0001c0004t0001g0069 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-217-12532C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962706 | ||||||
| chr9:92962751
|
C | G | 2 | a0001c0002t0004g0162a0001c0002t0004g0163 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-217-12487C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962751 | ||||||
| chr9:92962905
|
A | G | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-217-12333A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962905 | ||||||
| chr9:92962934
|
C | T | 4 | a0001c0002t0002g0217a0001c0002t0002g0218a0001c0002t0002g0222others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-217-12304C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962934 | ||||||
| chr9:92962939
|
C | CA | 96 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-217-12282dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92962939 | |||||
| chr9:92962939
|
CA | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0174a0001c0002t0002g0312others(6): Show | 9 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-217-12282delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92962939 | |||||
| chr9:92962959
|
A | AAAGAAAA others(1): Show |
39 | a0001c0001t0001g0004a0001c0002t0002g0184a0001c0002t0002g0193others(36): Show | 39 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-217-12277_-217-12 others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92962959 | |||||
| chr9:92962962
|
G | T | 37 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-217-12276G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92962962 | ||||||
| chr9:92963049
|
G | A | 1 | a0001c0005t0004g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-217-12189G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92963049 | ||||||
| chr9:92963244
|
C | T | 25 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(22): Show | 25 | HG00544.hp2 HG00735.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-217-11994C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92963244 | ||||||
| chr9:92963279
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-217-11959G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92963279 | ||||||
| chr9:92963598
|
G | A | 1 | a0001c0004t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-217-11640G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92963598 | ||||||
| chr9:92963792
|
G | A | 1 | a0001c0002t0004g0245 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-217-11446G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92963792 | ||||||
| chr9:92964051
|
G | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-11187G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964051 | ||||||
| chr9:92964165
|
C | CG | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-11072dupG | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92964165 | |||||
| chr9:92964721
|
C | T | 7 | a0001c0001t0001g0117a0001c0002t0004g0115a0001c0002t0004g0116others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-217-10517C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964721 | ||||||
| chr9:92964766
|
G | T | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-10472G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964766 | ||||||
| chr9:92964800
|
C | T | 8 | a0001c0001t0001g0117a0001c0002t0002g0312a0001c0002t0004g0115others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-217-10438C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964800 | ||||||
| chr9:92964878
|
C | T | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-217-10360C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964878 | ||||||
| chr9:92964961
|
G | A | 7 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0189others(4): Show | 7 | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-217-10277G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964961 | ||||||
| chr9:92964999
|
C | T | 43 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(40): Show | 43 | HG00544.hp2 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.-217-10239C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92964999 | ||||||
| chr9:92965150
|
G | C | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-10088G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965150 | ||||||
| chr9:92965176
|
C | T | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-217-10062C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965176 | ||||||
| chr9:92965231
|
G | C | 1 | a0001c0002t0004g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-217-10007G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965231 | ||||||
| chr9:92965250
|
T | C | 13 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(10): Show | 13 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-217-9988T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965250 | ||||||
| chr9:92965357
|
G | C | 7 | a0001c0002t0004g0008a0001c0002t0004g0177a0001c0002t0004g0178others(4): Show | 7 | HG01081.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-217-9881G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965357 | ||||||
| chr9:92965370
|
C | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-9868C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965370 | ||||||
| chr9:92965525
|
G | A | 73 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.-217-9713G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965525 | ||||||
| chr9:92965601
|
T | C | 43 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(40): Show | 43 | HG00544.hp2 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.-217-9637T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965601 | ||||||
| chr9:92965742
|
C | T | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-9496C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965742 | ||||||
| chr9:92965854
|
T | C | 2 | a0001c0005t0004g0005a0001c0005t0004g0006 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-217-9384T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965854 | ||||||
| chr9:92965994
|
A | G | 1 | a0001c0001t0005g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-217-9244A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92965994 | ||||||
| chr9:92966053
|
C | T | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-217-9185C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966053 | ||||||
| chr9:92966194
|
C | T | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-217-9044C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966194 | ||||||
| chr9:92966384
|
T | A | 16 | a0001c0001t0001g0100a0002c0003t0001g0059a0002c0003t0001g0073others(13): Show | 16 | HG00621.hp1 HG00741.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-217-8854T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966384 | ||||||
| chr9:92966385
|
G | A | 2 | a0001c0004t0001g0286a0001c0004t0001g0287 | 2 | HG00323.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-217-8853G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966385 | ||||||
| chr9:92966441
|
G | A | 13 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(10): Show | 13 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-217-8797G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966441 | ||||||
| chr9:92966459
|
G | C | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-8779G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966459 | ||||||
| chr9:92966609
|
A | G | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-217-8629A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966609 | ||||||
| chr9:92966632
|
C | T | 7 | a0001c0001t0001g0117a0001c0002t0004g0115a0001c0002t0004g0116others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-217-8606C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966632 | ||||||
| chr9:92966785
|
G | A | 4 | a0001c0001t0001g0117a0001c0002t0004g0116a0001c0002t0004g0118others(1): Show | 4 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-217-8453G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966785 | ||||||
| chr9:92966799
|
G | T | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-217-8439G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966799 | ||||||
| chr9:92966960
|
C | CT | 32 | a0001c0002t0002g0184a0001c0002t0002g0193a0001c0002t0002g0194others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-217-8264dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92966960 | |||||
| chr9:92966960
|
CT | C | 14 | a0001c0002t0002g0204a0001c0002t0004g0153a0001c0002t0004g0154others(11): Show | 14 | HG01081.hp1 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-217-8264delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92966960 | |||||
| chr9:92966973
|
T | G | 7 | a0001c0001t0001g0117a0001c0002t0004g0115a0001c0002t0004g0116others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-217-8265T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966973 | ||||||
| chr9:92966974
|
T | G | 28 | a0001c0001t0001g0053a0001c0001t0007g0313a0001c0001t0007g0314others(25): Show | 28 | HG00741.hp1 HG01081.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-217-8264T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966974 | ||||||
| chr9:92966975
|
G | T | 1 | a0001c0002t0002g0266 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-217-8263G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966975 | ||||||
| chr9:92966976
|
G | A | 49 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0091others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-217-8262G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92966976 | ||||||
| chr9:92967031
|
G | A | 71 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.-217-8207G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967031 | ||||||
| chr9:92967064
|
C | T | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-217-8174C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967064 | ||||||
| chr9:92967107
|
G | A | 82 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-217-8131G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967107 | ||||||
| chr9:92967203
|
T | C | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-217-8035T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967203 | ||||||
| chr9:92967305
|
AT | A | 31 | a0001c0002t0002g0184a0001c0002t0002g0193a0001c0002t0002g0223others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-217-7931delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92967305 | |||||
| chr9:92967349
|
G | A | 3 | a0001c0001t0003g0272a0001c0001t0003g0274a0001c0001t0003g0319 | 3 | HG02027.hp1 NA18975.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-217-7889G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967349 | ||||||
| chr9:92967543
|
C | A | 7 | a0001c0001t0001g0117a0001c0002t0004g0115a0001c0002t0004g0116others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-217-7695C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967543 | ||||||
| chr9:92967837
|
T | C | 23 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(20): Show | 23 | HG00544.hp2 HG00735.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-217-7401T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92967837 | ||||||
| chr9:92968162
|
G | A | 1 | a0001c0002t0002g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-217-7076G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968162 | ||||||
| chr9:92968282
|
G | A | 1 | a0001c0002t0002g0257 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-217-6956G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968282 | ||||||
| chr9:92968475
|
T | C | 30 | a0001c0001t0001g0117a0001c0001t0005g0011a0001c0001t0005g0013others(27): Show | 30 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-217-6763T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968475 | ||||||
| chr9:92968529
|
TA | T | 14 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(11): Show | 14 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.-217-6707delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92968529 | |||||
| chr9:92968603
|
C | T | 167 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-217-6635C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968603 | ||||||
| chr9:92968607
|
C | CT | 30 | a0001c0001t0001g0117a0001c0001t0001g0288a0001c0001t0005g0011others(27): Show | 30 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-217-6617dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92968607 | |||||
| chr9:92968607
|
C | CTT | 166 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-217-6618_-217-661 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92968607 | |||||
| chr9:92968613
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-217-6625T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968613 | ||||||
| chr9:92968758
|
C | T | 37 | a0001c0001t0001g0117a0001c0001t0005g0011a0001c0001t0005g0013others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.-217-6480C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92968758 | ||||||
| chr9:92969209
|
G | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0029 | 2 | NA18940.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-217-6029G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969209 | ||||||
| chr9:92969245
|
C | T | 1 | a0001c0002t0004g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-217-5993C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969245 | ||||||
| chr9:92969310
|
C | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(33): Show | 36 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-217-5928C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969310 | ||||||
| chr9:92969412
|
C | T | 6 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-5826C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969412 | ||||||
| chr9:92969517
|
G | A | 2 | a0001c0009t0003g0289a0001c0009t0003g0290 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-217-5721G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969517 | ||||||
| chr9:92969589
|
G | A | 1 | a0001c0012t0003g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-217-5649G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969589 | ||||||
| chr9:92969601
|
G | T | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-217-5637G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969601 | ||||||
| chr9:92969679
|
C | A | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.-217-5559C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969679 | ||||||
| chr9:92969809
|
G | T | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-217-5429G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969809 | ||||||
| chr9:92969988
|
C | T | 9 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-217-5250C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969988 | ||||||
| chr9:92969993
|
C | T | 2 | a0001c0002t0002g0246a0001c0002t0004g0245 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-217-5245C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92969993 | ||||||
| chr9:92970031
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-5207G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970031 | ||||||
| chr9:92970097
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-217-5141A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970097 | ||||||
| chr9:92970124
|
C | T | 18 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(15): Show | 18 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.-217-5114C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970124 | ||||||
| chr9:92970127
|
G | A | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-5111G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970127 | ||||||
| chr9:92970264
|
G | C | 199 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-217-4974G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970264 | ||||||
| chr9:92970315
|
A | G | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-217-4923A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970315 | ||||||
| chr9:92970550
|
G | C | 61 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-217-4688G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970550 | ||||||
| chr9:92970550
|
GCCACTGT others(7): Show |
G | 1 | a0001c0001t0001g0271 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-217-4686_-217-467 others(18): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92970550 | |||||
| chr9:92970621
|
C | A | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-4617C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970621 | ||||||
| chr9:92970626
|
G | C | 1 | a0002c0003t0005g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-217-4612G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970626 | ||||||
| chr9:92970652
|
G | A | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-217-4586G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970652 | ||||||
| chr9:92970855
|
C | G | 1 | a0002c0003t0001g0102 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-217-4383C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970855 | ||||||
| chr9:92970999
|
G | T | 1 | a0001c0012t0003g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-217-4239G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92970999 | ||||||
| chr9:92971076
|
C | G | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-4162C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971076 | ||||||
| chr9:92971203
|
G | A | 1 | a0001c0002t0006g0020 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-217-4035G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971203 | ||||||
| chr9:92971291
|
C | T | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-217-3947C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971291 | ||||||
| chr9:92971317
|
G | A | 28 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(25): Show | 28 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-217-3921G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971317 | ||||||
| chr9:92971399
|
C | T | 1 | a0001c0021t0018g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-217-3839C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971399 | ||||||
| chr9:92971540
|
A | T | 1 | a0001c0018t0014g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-217-3698A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971540 | ||||||
| chr9:92971541
|
TTTTTC | T | 18 | a0001c0001t0001g0054a0001c0001t0001g0128a0001c0001t0001g0139others(15): Show | 18 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-217-3672_-217-366 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971541 | |||||
| chr9:92971544
|
T | TTCTTC | 3 | a0001c0005t0004g0005a0001c0010t0004g0182a0001c0010t0004g0183 | 3 | HG02109.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-217-3690_-217-368 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971544 | |||||
| chr9:92971549
|
T | C | 2 | a0001c0002t0004g0008a0001c0005t0004g0006 | 2 | HG01081.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-217-3689T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971549 | ||||||
| chr9:92971561
|
CTTTTCT | C | 134 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-217-3672_-217-366 others(10): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971561 | |||||
| chr9:92971561
|
CTTTTCTT | C | 28 | a0001c0001t0001g0117a0001c0001t0001g0131a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-217-3672_-217-366 others(11): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971561 | |||||
| chr9:92971561
|
CTTTTCTT others(2): Show |
C | 7 | a0001c0001t0005g0031a0001c0001t0007g0313a0001c0001t0007g0314others(4): Show | 7 | HG02080.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-217-3672_-217-366 others(13): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971561 | |||||
| chr9:92971561
|
CTTTTCTT others(7): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-217-3672_-217-365 others(18): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971561 | |||||
| chr9:92971561
|
CTTTTCTT others(9): Show |
C | 2 | a0001c0001t0011g0180a0001c0021t0018g0181 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-217-3672_-217-365 others(20): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971561 | |||||
| chr9:92971566
|
C | CT | 6 | a0001c0002t0002g0215a0001c0002t0002g0222a0001c0002t0002g0267others(3): Show | 6 | HG00673.hp2 HG01934.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-217-3645dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971566 | |||||
| chr9:92971566
|
CT | C | 36 | a0001c0001t0001g0186a0001c0002t0002g0184a0001c0002t0002g0193others(33): Show | 36 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-217-3645delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971566 | |||||
| chr9:92971566
|
CTT | C | 8 | a0001c0002t0002g0266a0001c0002t0002g0312a0001c0002t0004g0177others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-217-3646_-217-364 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971566 | |||||
| chr9:92971566
|
CTTT | C | 18 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(15): Show | 18 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-217-3647_-217-364 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92971566 | |||||
| chr9:92971573
|
T | C | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-217-3665T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971573 | ||||||
| chr9:92971577
|
T | C | 1 | a0001c0002t0002g0312 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-217-3661T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971577 | ||||||
| chr9:92971582
|
T | A | 1 | a0001c0021t0018g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-217-3656T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971582 | ||||||
| chr9:92971602
|
A | G | 1 | a0001c0018t0014g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-217-3636A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971602 | ||||||
| chr9:92971634
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-3604G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971634 | ||||||
| chr9:92971680
|
T | A | 192 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-217-3558T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971680 | ||||||
| chr9:92971700
|
C | T | 1 | a0001c0002t0004g0119 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-217-3538C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971700 | ||||||
| chr9:92971784
|
G | A | 1 | a0002c0013t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-217-3454G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92971784 | ||||||
| chr9:92972061
|
GTAA | G | 156 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-217-3175_-217-317 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92972061 | |||||
| chr9:92972236
|
G | A | 18 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(15): Show | 18 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.-217-3002G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972236 | ||||||
| chr9:92972338
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-2900G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972338 | ||||||
| chr9:92972375
|
C | A | 2 | a0001c0004t0001g0056a0001c0004t0003g0055 | 2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-217-2863C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972375 | ||||||
| chr9:92972375
|
C | G | 153 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-217-2863C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972375 | ||||||
| chr9:92972425
|
T | C | 200 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-217-2813T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972425 | ||||||
| chr9:92972452
|
C | CA | 27 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0141others(24): Show | 27 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-217-2767dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92972452 | |||||
| chr9:92972452
|
CA | C | 22 | a0001c0001t0003g0066a0001c0001t0005g0013a0001c0002t0004g0153others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-217-2767delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92972452 | |||||
| chr9:92972572
|
C | T | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-217-2666C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972572 | ||||||
| chr9:92972637
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-217-2601G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972637 | ||||||
| chr9:92972689
|
TA | T | 156 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-217-2548delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972689 | ||||||
| chr9:92972721
|
G | C | 2 | a0001c0002t0002g0233a0001c0002t0002g0266 | 2 | NA18983.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-217-2517G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972721 | ||||||
| chr9:92972780
|
C | CTG | 8 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-217-2442_-217-244 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92972780 | |||||
| chr9:92972838
|
C | G | 1 | a0001c0002t0002g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-217-2400C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92972838 | ||||||
| chr9:92973106
|
A | AT | 27 | a0001c0001t0001g0221a0001c0002t0002g0190a0001c0002t0002g0214others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.-217-2106dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
A | ATT | 13 | a0001c0002t0002g0184a0001c0002t0002g0242a0001c0002t0002g0258others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-217-2107_-217-210 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
AT | A | 45 | a0001c0001t0001g0092a0001c0001t0001g0117a0001c0001t0005g0011others(42): Show | 45 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-217-2106delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
ATT | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0091others(13): Show | 16 | HG01361.hp1 HG01361.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-217-2107_-217-210 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
ATTT | A | 56 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0094others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.-217-2108_-217-210 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
ATTTT | A | 59 | a0001c0001t0001g0053a0001c0001t0001g0123a0001c0001t0001g0125others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-217-2109_-217-210 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973106
|
ATTTTT | A | 33 | a0001c0001t0001g0151a0001c0001t0001g0271a0001c0001t0001g0276others(30): Show | 33 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.-217-2110_-217-210 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92973106 | |||||
| chr9:92973192
|
G | A | 155 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-217-2046G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973192 | ||||||
| chr9:92973240
|
A | G | 321 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-217-1998A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973240 | ||||||
| chr9:92973329
|
G | T | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-217-1909G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973329 | ||||||
| chr9:92973395
|
G | A | 1 | a0001c0002t0002g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-217-1843G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973395 | ||||||
| chr9:92973791
|
G | A | 1 | a0001c0002t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-217-1447G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973791 | ||||||
| chr9:92973982
|
T | C | 200 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-217-1256T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92973982 | ||||||
| chr9:92974100
|
T | TTCG | 27 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-217-1137_-217-113 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 92974100 | |||||
| chr9:92974102
|
T | A | 27 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-217-1136T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974102 | ||||||
| chr9:92974103
|
T | G | 27 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-217-1135T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974103 | ||||||
| chr9:92974104
|
G | A | 11 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0004t0001g0065others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-217-1134G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974104 | ||||||
| chr9:92974162
|
T | C | 28 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(25): Show | 28 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-217-1076T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974162 | ||||||
| chr9:92974172
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-1066G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974172 | ||||||
| chr9:92974393
|
G | A | 2 | a0001c0005t0004g0005a0001c0005t0004g0006 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-217-845G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974393 | ||||||
| chr9:92974533
|
G | A | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-217-705G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974533 | ||||||
| chr9:92974665
|
T | C | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-217-573T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974665 | ||||||
| chr9:92974682
|
T | A | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-217-556T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974682 | ||||||
| chr9:92974933
|
C | T | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-217-305C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92974933 | ||||||
| chr9:92975003
|
C | T | 40 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0281others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.-217-235C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92975003 | ||||||
| chr9:92975122
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-217-116T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92975122 | ||||||
| chr9:92975230
|
C | T | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | splice_region_variant&intron_variant | LOW | c.-217-8C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 1/17 | chr9 | 92975230 | ||||||
| chr9:92975463
|
C | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-50+58C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975463 | ||||||
| chr9:92975593
|
C | T | 39 | a0001c0002t0002g0184a0001c0002t0002g0193a0001c0002t0002g0223others(36): Show | 39 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50+188C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975593 | ||||||
| chr9:92975594
|
A | G | 275 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-50+189A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975594 | ||||||
| chr9:92975682
|
G | A | 1 | a0001c0002t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-50+277G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975682 | ||||||
| chr9:92975728
|
T | C | 1 | a0001c0002t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-50+323T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975728 | ||||||
| chr9:92975780
|
T | TGAG | 5 | a0001c0001t0001g0057a0001c0001t0007g0315a0001c0002t0004g0001others(2): Show | 5 | HG01891.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+393_-50+395dup others(3): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 92975780 | |||||
| chr9:92975780
|
T | TGAGGAG | 27 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50+390_-50+395dup others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 92975780 | |||||
| chr9:92975780
|
T | TGAGGAGG others(5): Show |
1 | a0001c0001t0005g0028 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-50+384_-50+395dup others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 92975780 | |||||
| chr9:92975968
|
G | T | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-49-240G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92975968 | ||||||
| chr9:92976101
|
C | G | 209 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-49-107C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 2/17 | chr9 | 92976101 | ||||||
| chr9:92976865
|
C | G | 1 | a0001c0001t0005g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.453+156C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92976865 | ||||||
| chr9:92977044
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+335G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977044 | ||||||
| chr9:92977055
|
A | T | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+346A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977055 | ||||||
| chr9:92977373
|
C | G | 209 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.453+664C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977373 | ||||||
| chr9:92977400
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.453+691C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977400 | ||||||
| chr9:92977469
|
A | C | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+760A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977469 | ||||||
| chr9:92977501
|
A | G | 1 | a0001c0002t0004g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.453+792A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977501 | ||||||
| chr9:92977578
|
A | G | 1 | a0001c0002t0002g0224 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.453+869A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977578 | ||||||
| chr9:92977622
|
A | T | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+913A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977622 | ||||||
| chr9:92977854
|
T | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1145T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977854 | ||||||
| chr9:92977856
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1147G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977856 | ||||||
| chr9:92977857
|
T | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1148T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977857 | ||||||
| chr9:92977859
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1150G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977859 | ||||||
| chr9:92977871
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1162C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977871 | ||||||
| chr9:92977883
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1174A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977883 | ||||||
| chr9:92977886
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1177C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977886 | ||||||
| chr9:92977888
|
T | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1179T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977888 | ||||||
| chr9:92977895
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1186G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977895 | ||||||
| chr9:92977897
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1188G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977897 | ||||||
| chr9:92977898
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1189A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977898 | ||||||
| chr9:92977900
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1191C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977900 | ||||||
| chr9:92977902
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1193G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977902 | ||||||
| chr9:92977903
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1194A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977903 | ||||||
| chr9:92977905
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1196G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977905 | ||||||
| chr9:92977907
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1198C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977907 | ||||||
| chr9:92977909
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1200G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977909 | ||||||
| chr9:92977910
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1201A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977910 | ||||||
| chr9:92977911
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1202C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977911 | ||||||
| chr9:92977913
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1204G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977913 | ||||||
| chr9:92977918
|
G | C | 1 | a0001c0001t0005g0038 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.453+1209G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977918 | ||||||
| chr9:92977918
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1209G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977918 | ||||||
| chr9:92977920
|
C | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1211C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977920 | ||||||
| chr9:92977922
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1213C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977922 | ||||||
| chr9:92977924
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1215G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977924 | ||||||
| chr9:92977925
|
T | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1216T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977925 | ||||||
| chr9:92977926
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1217G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977926 | ||||||
| chr9:92977927
|
G | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1218G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977927 | ||||||
| chr9:92977928
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1219C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977928 | ||||||
| chr9:92977929
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1220A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977929 | ||||||
| chr9:92977932
|
A | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1223A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977932 | ||||||
| chr9:92977934
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1225G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977934 | ||||||
| chr9:92977938
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1229C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977938 | ||||||
| chr9:92977939
|
C | T | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1230C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977939 | ||||||
| chr9:92977952
|
G | A | 1 | a0002c0007t0004g0231 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.453+1243G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92977952 | ||||||
| chr9:92978049
|
G | C | 9 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0004t0001g0065others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+1340G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978049 | ||||||
| chr9:92978101
|
G | A | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+1392G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978101 | ||||||
| chr9:92978143
|
G | A | 1 | a0001c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.453+1434G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978143 | ||||||
| chr9:92978151
|
A | T | 1 | a0001c0001t0007g0316 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.453+1442A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978151 | ||||||
| chr9:92978258
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.453+1549G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978258 | ||||||
| chr9:92978282
|
C | CA | 70 | a0001c0001t0001g0004a0001c0001t0001g0117a0001c0001t0001g0123others(67): Show | 70 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.453+1590dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92978282 | |||||
| chr9:92978306
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.453+1597A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978306 | ||||||
| chr9:92978413
|
A | AC | 20 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0001g0140others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.453+1711dupC | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92978413 | |||||
| chr9:92978490
|
A | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.453+1781A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978490 | ||||||
| chr9:92978498
|
A | G | 1 | a0001c0002t0002g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.453+1789A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978498 | ||||||
| chr9:92978614
|
G | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.453+1905G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978614 | ||||||
| chr9:92978673
|
T | TC | 7 | a0001c0001t0001g0050a0001c0001t0001g0137a0001c0001t0001g0281others(4): Show | 7 | HG01099.hp1 HG01515.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+1970dupC | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92978673 | |||||
| chr9:92978678
|
C | G | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+1969C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978678 | ||||||
| chr9:92978678
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0125others(23): Show | 26 | HG00609.hp1 HG01070.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.453+1969C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978678 | ||||||
| chr9:92978691
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.453+1982C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978691 | ||||||
| chr9:92978724
|
C | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0252 | 2 | NA19067.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.453+2015C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978724 | ||||||
| chr9:92978766
|
GCCCCTCC others(3): Show |
G | 206 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.453+2079_453+2088d others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92978766 | |||||
| chr9:92978788
|
C | T | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+2079C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978788 | ||||||
| chr9:92978792
|
C | T | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+2083C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978792 | ||||||
| chr9:92978808
|
C | T | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+2099C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92978808 | ||||||
| chr9:92979112
|
C | A | 1 | a0002c0003t0001g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.453+2403C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979112 | ||||||
| chr9:92979303
|
G | A | 1 | a0001c0001t0003g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.453+2594G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979303 | ||||||
| chr9:92979324
|
T | A | 61 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.453+2615T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979324 | ||||||
| chr9:92979537
|
G | T | 235 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.453+2828G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979537 | ||||||
| chr9:92979573
|
G | A | 8 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.453+2864G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979573 | ||||||
| chr9:92979597
|
A | G | 1 | a0001c0002t0004g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.453+2888A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979597 | ||||||
| chr9:92979652
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.453+2943T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979652 | ||||||
| chr9:92979837
|
G | T | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+3128G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979837 | ||||||
| chr9:92979861
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0005g0034a0001c0001t0005g0041others(1): Show | 4 | HG00323.hp2 HG00735.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+3152T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979861 | ||||||
| chr9:92979921
|
CT | C | 4 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0282others(1): Show | 4 | NA18966.hp2 NA18969.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+3213delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92979921 | ||||||
| chr9:92979954
|
C | CTT | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+3255_453+3256d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92979954 | |||||
| chr9:92980030
|
A | AT | 161 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.453+3335dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92980030 | |||||
| chr9:92980133
|
G | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+3424G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980133 | ||||||
| chr9:92980261
|
C | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+3552C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980261 | ||||||
| chr9:92980308
|
C | T | 30 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+3599C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980308 | ||||||
| chr9:92980318
|
C | T | 1 | a0001c0002t0004g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.453+3609C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980318 | ||||||
| chr9:92980369
|
T | G | 6 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+3660T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980369 | ||||||
| chr9:92980471
|
T | C | 1 | a0001c0001t0005g0041 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.453+3762T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980471 | ||||||
| chr9:92980544
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.453+3835A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980544 | ||||||
| chr9:92980560
|
AT | A | 19 | a0001c0002t0002g0189a0001c0002t0004g0153a0001c0002t0004g0154others(16): Show | 19 | HG01081.hp1 HG01884.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.453+3863delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92980560 | |||||
| chr9:92980699
|
C | T | 1 | a0001c0020t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.453+3990C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980699 | ||||||
| chr9:92980745
|
G | A | 30 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+4036G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980745 | ||||||
| chr9:92980948
|
G | A | 4 | a0001c0002t0002g0217a0001c0002t0002g0218a0001c0002t0002g0222others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+4239G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92980948 | ||||||
| chr9:92980970
|
C | CA | 30 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0003g0278others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+4273dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92980970 | |||||
| chr9:92981135
|
G | A | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.453+4426G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981135 | ||||||
| chr9:92981144
|
G | A | 7 | a0001c0004t0001g0093a0001c0004t0001g0096a0001c0004t0001g0111others(4): Show | 7 | HG01243.hp2 HG01361.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+4435G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981144 | ||||||
| chr9:92981368
|
C | CA | 195 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.453+4675dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92981368 | |||||
| chr9:92981368
|
C | CAA | 9 | a0001c0001t0001g0139a0001c0004t0001g0096a0001c0004t0001g0112others(6): Show | 9 | HG01243.hp2 HG01433.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.453+4674_453+4675d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92981368 | |||||
| chr9:92981487
|
A | G | 1 | a0002c0013t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.453+4778A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981487 | ||||||
| chr9:92981662
|
C | T | 11 | a0001c0001t0003g0089a0001c0001t0007g0316a0001c0001t0007g0318others(8): Show | 11 | HG00438.hp1 HG00609.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+4953C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981662 | ||||||
| chr9:92981750
|
C | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+5041C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981750 | ||||||
| chr9:92981870
|
A | G | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+5161A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981870 | ||||||
| chr9:92981914
|
G | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+5205G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981914 | ||||||
| chr9:92981917
|
T | C | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+5208T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92981917 | ||||||
| chr9:92982392
|
A | T | 1 | a0001c0002t0002g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.453+5683A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982392 | ||||||
| chr9:92982509
|
G | A | 2 | a0001c0004t0001g0068a0001c0004t0001g0069 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.453+5800G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982509 | ||||||
| chr9:92982568
|
A | AT | 203 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0053others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.453+5871dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92982568 | |||||
| chr9:92982633
|
C | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+5924C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982633 | ||||||
| chr9:92982688
|
A | G | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+5979A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982688 | ||||||
| chr9:92982736
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.453+6027C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982736 | ||||||
| chr9:92982748
|
C | A | 1 | a0001c0002t0002g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+6039C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982748 | ||||||
| chr9:92982814
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.453+6105G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982814 | ||||||
| chr9:92982845
|
A | G | 226 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.453+6136A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982845 | ||||||
| chr9:92982860
|
T | C | 13 | a0001c0002t0002g0226a0001c0002t0002g0227a0001c0002t0002g0228others(10): Show | 13 | HG01943.hp1 NA18959.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.453+6151T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982860 | ||||||
| chr9:92982861
|
G | C | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.453+6152G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92982861 | ||||||
| chr9:92983041
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.453+6332G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983041 | ||||||
| chr9:92983189
|
G | C | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+6480G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983189 | ||||||
| chr9:92983350
|
G | A | 2 | a0002c0007t0004g0232a0002c0007t0004g0237 | 2 | HG00621.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.453+6641G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983350 | ||||||
| chr9:92983439
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0011g0180a0001c0021t0018g0181 | 3 | HG01255.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.453+6730G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983439 | ||||||
| chr9:92983449
|
C | T | 2 | a0001c0004t0001g0056a0001c0004t0003g0055 | 2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.453+6740C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983449 | ||||||
| chr9:92983450
|
G | A | 1 | a0001c0002t0004g0119 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.453+6741G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983450 | ||||||
| chr9:92983540
|
C | T | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+6831C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983540 | ||||||
| chr9:92983875
|
T | C | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+7166T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92983875 | ||||||
| chr9:92984178
|
C | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+7469C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92984178 | ||||||
| chr9:92984371
|
T | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0014t0003g0049 | 3 | HG02818.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.453+7662T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92984371 | ||||||
| chr9:92984385
|
G | A | 2 | a0001c0001t0003g0284a0001c0001t0003g0295 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.453+7676G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92984385 | ||||||
| chr9:92984654
|
A | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+7945A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92984654 | ||||||
| chr9:92984722
|
G | T | 5 | a0001c0002t0004g0008a0001c0005t0004g0005a0001c0005t0004g0006others(2): Show | 5 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+8013G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92984722 | ||||||
| chr9:92984811
|
CT | C | 31 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(28): Show | 31 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.453+8116delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92984811 | |||||
| chr9:92985010
|
G | T | 1 | a0001c0004t0001g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.453+8301G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985010 | ||||||
| chr9:92985056
|
T | C | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+8347T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985056 | ||||||
| chr9:92985089
|
G | A | 1 | a0001c0002t0002g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.453+8380G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985089 | ||||||
| chr9:92985107
|
T | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.453+8398T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985107 | ||||||
| chr9:92985324
|
C | T | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+8615C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985324 | ||||||
| chr9:92985610
|
C | T | 18 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(15): Show | 18 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.453+8901C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985610 | ||||||
| chr9:92985704
|
C | T | 39 | a0001c0002t0002g0184a0001c0002t0002g0193a0001c0002t0002g0194others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.453+8995C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985704 | ||||||
| chr9:92985768
|
G | A | 1 | a0004c0019t0001g0168 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.453+9059G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985768 | ||||||
| chr9:92985768
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.453+9059G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985768 | ||||||
| chr9:92985770
|
A | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+9061A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985770 | ||||||
| chr9:92985781
|
T | C | 1 | a0002c0003t0003g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.453+9072T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985781 | ||||||
| chr9:92985803
|
G | C | 30 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+9094G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985803 | ||||||
| chr9:92985987
|
G | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01074.hp2 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+9278G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985987 | ||||||
| chr9:92985991
|
C | T | 1 | a0001c0020t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.453+9282C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985991 | ||||||
| chr9:92985992
|
A | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+9283A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92985992 | ||||||
| chr9:92986359
|
G | C | 1 | a0001c0004t0010g0062 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.453+9650G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92986359 | ||||||
| chr9:92986535
|
G | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.453+9826G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92986535 | ||||||
| chr9:92986628
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.453+9919T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92986628 | ||||||
| chr9:92986664
|
G | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0004t0001g0093others(6): Show | 9 | HG01243.hp2 HG01361.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+9955G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92986664 | ||||||
| chr9:92986771
|
A | G | 2 | a0001c0002t0002g0247a0001c0002t0002g0256 | 2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.453+10062A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92986771 | ||||||
| chr9:92987075
|
C | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+10366C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987075 | ||||||
| chr9:92987159
|
G | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0004t0001g0093others(6): Show | 9 | HG01243.hp2 HG01361.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+10450G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987159 | ||||||
| chr9:92987325
|
G | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.453+10616G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987325 | ||||||
| chr9:92987343
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0138 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.453+10634A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987343 | ||||||
| chr9:92987349
|
G | A | 1 | a0001c0002t0002g0246 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.453+10640G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987349 | ||||||
| chr9:92987364
|
G | A | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+10655G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987364 | ||||||
| chr9:92987425
|
C | T | 1 | a0001c0030t0017g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.453+10716C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987425 | ||||||
| chr9:92987431
|
CA | C | 204 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.453+10736delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92987431 | |||||
| chr9:92987454
|
G | A | 8 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.453+10745G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987454 | ||||||
| chr9:92987548
|
G | C | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.453+10839G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987548 | ||||||
| chr9:92987577
|
C | T | 2 | a0001c0002t0004g0115a0001c0002t0004g0121 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.453+10868C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987577 | ||||||
| chr9:92987618
|
G | A | 1 | a0001c0002t0002g0266 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.453+10909G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987618 | ||||||
| chr9:92987623
|
T | A | 209 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.453+10914T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987623 | ||||||
| chr9:92987779
|
G | A | 30 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0005g0011others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+11070G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987779 | ||||||
| chr9:92987819
|
T | C | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.453+11110T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987819 | ||||||
| chr9:92987824
|
G | A | 1 | a0001c0004t0001g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.453+11115G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987824 | ||||||
| chr9:92987903
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.453+11194A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92987903 | ||||||
| chr9:92987985
|
AT | A | 9 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+11280delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92987985 | |||||
| chr9:92988046
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.453+11337G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988046 | ||||||
| chr9:92988118
|
G | A | 1 | a0001c0002t0002g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.453+11409G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988118 | ||||||
| chr9:92988448
|
C | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+11739C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988448 | ||||||
| chr9:92988449
|
T | G | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.453+11740T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988449 | ||||||
| chr9:92988517
|
C | T | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+11808C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988517 | ||||||
| chr9:92988734
|
A | G | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+12025A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988734 | ||||||
| chr9:92988838
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.453+12129G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988838 | ||||||
| chr9:92988857
|
T | C | 4 | a0001c0002t0004g0177a0001c0002t0004g0178a0001c0002t0004g0311others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+12148T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988857 | ||||||
| chr9:92988958
|
C | T | 1 | a0001c0004t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.453+12249C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92988958 | ||||||
| chr9:92989257
|
G | A | 2 | a0001c0002t0004g0162a0001c0002t0004g0163 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.453+12548G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989257 | ||||||
| chr9:92989340
|
C | G | 1 | a0002c0003t0001g0102 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.453+12631C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989340 | ||||||
| chr9:92989354
|
C | G | 1 | a0001c0002t0002g0241 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.453+12645C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989354 | ||||||
| chr9:92989554
|
A | G | 8 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+12845A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989554 | ||||||
| chr9:92989580
|
A | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.453+12871A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989580 | ||||||
| chr9:92989590
|
T | C | 1 | a0001c0001t0008g0040 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.453+12881T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989590 | ||||||
| chr9:92989614
|
G | GT | 15 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(12): Show | 15 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.453+12905_453+1290 others(5): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989614 | ||||||
| chr9:92989615
|
A | T | 15 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(12): Show | 15 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.453+12906A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989615 | ||||||
| chr9:92989635
|
A | G | 8 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.453+12926A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989635 | ||||||
| chr9:92989687
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0003g0308a0001c0002t0004g0008others(6): Show | 9 | HG01081.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.453+12978G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989687 | ||||||
| chr9:92989726
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0005g0031 | 2 | HG02080.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.453+13017G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989726 | ||||||
| chr9:92989919
|
G | GT | 8 | a0001c0001t0001g0004a0001c0001t0007g0314a0001c0001t0007g0315others(5): Show | 8 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-12988dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92989919 | |||||
| chr9:92989919
|
GT | G | 288 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.454-12988delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92989919 | |||||
| chr9:92989926
|
T | G | 1 | a0002c0027t0004g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.454-12999T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989926 | ||||||
| chr9:92989927
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.454-12998T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92989927 | ||||||
| chr9:92990139
|
A | G | 4 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(1): Show | 4 | HG00408.hp2 HG02027.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-12786A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990139 | ||||||
| chr9:92990175
|
C | T | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.454-12750C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990175 | ||||||
| chr9:92990225
|
C | T | 1 | a0001c0002t0002g0247 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.454-12700C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990225 | ||||||
| chr9:92990623
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0004t0001g0082others(7): Show | 10 | HG01243.hp2 HG01361.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-12302T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990623 | ||||||
| chr9:92990681
|
A | G | 2 | a0001c0002t0004g0178a0001c0002t0004g0311 | 2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.454-12244A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990681 | ||||||
| chr9:92990888
|
T | C | 1 | a0002c0003t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.454-12037T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92990888 | ||||||
| chr9:92991037
|
C | T | 56 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.454-11888C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991037 | ||||||
| chr9:92991065
|
A | ATTTG | 12 | a0001c0001t0001g0092a0001c0002t0002g0191a0001c0002t0004g0153others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.454-11832_454-1182 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92991065 | |||||
| chr9:92991065
|
ATTTGTTT others(1): Show |
A | 5 | a0001c0001t0001g0151a0001c0002t0002g0203a0001c0002t0004g0001others(2): Show | 5 | HG01255.hp1 HG01891.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-11836_454-1182 others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92991065 | |||||
| chr9:92991153
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-11772C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991153 | ||||||
| chr9:92991361
|
G | A | 2 | a0001c0002t0002g0205a0001c0002t0002g0226 | 2 | HG03654.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.454-11564G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991361 | ||||||
| chr9:92991374
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.454-11551C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991374 | ||||||
| chr9:92991631
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.454-11294C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991631 | ||||||
| chr9:92991632
|
G | A | 1 | a0001c0002t0002g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454-11293G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991632 | ||||||
| chr9:92991637
|
G | A | 1 | a0001c0004t0003g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.454-11288G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991637 | ||||||
| chr9:92991664
|
G | A | 20 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(17): Show | 20 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.454-11261G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991664 | ||||||
| chr9:92991727
|
A | G | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.454-11198A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991727 | ||||||
| chr9:92991794
|
T | G | 1 | a0001c0001t0011g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.454-11131T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991794 | ||||||
| chr9:92991837
|
T | G | 2 | a0001c0005t0004g0005a0001c0005t0004g0006 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.454-11088T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991837 | ||||||
| chr9:92991862
|
T | C | 2 | a0001c0001t0007g0313a0001c0001t0011g0317 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.454-11063T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991862 | ||||||
| chr9:92991998
|
G | A | 1 | a0001c0001t0003g0303 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.454-10927G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92991998 | ||||||
| chr9:92992026
|
G | C | 3 | a0001c0001t0003g0277a0001c0001t0003g0306a0001c0001t0003g0307 | 3 | HG00099.hp1 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.454-10899G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992026 | ||||||
| chr9:92992367
|
T | C | 2 | a0001c0002t0002g0247a0001c0002t0002g0256 | 2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.454-10558T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992367 | ||||||
| chr9:92992389
|
T | G | 20 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(17): Show | 20 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.454-10536T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992389 | ||||||
| chr9:92992448
|
T | C | 33 | a0001c0001t0005g0033a0001c0002t0002g0184a0001c0002t0002g0193others(30): Show | 33 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.454-10477T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992448 | ||||||
| chr9:92992721
|
G | A | 2 | a0001c0002t0002g0207a0001c0002t0002g0209 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.454-10204G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992721 | ||||||
| chr9:92992916
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0005g0032a0001c0001t0005g0034others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-10009G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92992916 | ||||||
| chr9:92993686
|
A | G | 26 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0281others(23): Show | 26 | HG00099.hp2 HG00408.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-9239A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92993686 | ||||||
| chr9:92993696
|
A | G | 4 | a0001c0002t0002g0203a0001c0002t0004g0001a0001c0008t0004g0002others(1): Show | 4 | HG01891.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-9229A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92993696 | ||||||
| chr9:92993789
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-9136A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92993789 | ||||||
| chr9:92993918
|
A | G | 1 | a0002c0003t0001g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.454-9007A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92993918 | ||||||
| chr9:92993949
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.454-8976A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92993949 | ||||||
| chr9:92994094
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.454-8831C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994094 | ||||||
| chr9:92994130
|
C | A | 1 | a0001c0012t0003g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.454-8795C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994130 | ||||||
| chr9:92994149
|
A | T | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-8776A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994149 | ||||||
| chr9:92994184
|
G | T | 1 | a0001c0001t0003g0302 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.454-8741G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994184 | ||||||
| chr9:92994216
|
G | T | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-8709G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994216 | ||||||
| chr9:92994414
|
G | A | 1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.454-8511G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994414 | ||||||
| chr9:92994950
|
A | G | 1 | a0001c0004t0003g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.454-7975A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994950 | ||||||
| chr9:92994959
|
T | C | 2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.454-7966T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994959 | ||||||
| chr9:92994965
|
T | A | 4 | a0001c0002t0002g0203a0001c0002t0004g0001a0001c0008t0004g0002others(1): Show | 4 | HG01891.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-7960T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92994965 | ||||||
| chr9:92995099
|
T | C | 1 | a0001c0002t0002g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454-7826T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995099 | ||||||
| chr9:92995100
|
C | T | 1 | a0001c0002t0004g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454-7825C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995100 | ||||||
| chr9:92995324
|
C | T | 56 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.454-7601C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995324 | ||||||
| chr9:92995328
|
T | C | 1 | a0001c0001t0016g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.454-7597T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995328 | ||||||
| chr9:92995422
|
A | T | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-7503A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995422 | ||||||
| chr9:92995498
|
C | A | 1 | a0001c0001t0008g0012 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.454-7427C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995498 | ||||||
| chr9:92995621
|
TA | T | 5 | a0001c0002t0004g0116a0001c0002t0004g0118a0001c0002t0004g0119others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-7303delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995621 | ||||||
| chr9:92995789
|
G | A | 2 | a0001c0002t0002g0207a0001c0002t0002g0209 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.454-7136G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995789 | ||||||
| chr9:92995936
|
C | CT | 6 | a0001c0001t0003g0277a0001c0001t0003g0306a0001c0001t0003g0307others(3): Show | 6 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-6980dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92995936 | |||||
| chr9:92995951
|
G | A | 1 | a0001c0002t0002g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.454-6974G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92995951 | ||||||
| chr9:92996171
|
T | G | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.454-6754T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996171 | ||||||
| chr9:92996198
|
A | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.454-6727A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996198 | ||||||
| chr9:92996315
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-6610G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996315 | ||||||
| chr9:92996565
|
T | C | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-6360T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996565 | ||||||
| chr9:92996627
|
T | C | 3 | a0001c0001t0003g0066a0001c0004t0010g0062a0001c0004t0010g0067 | 3 | HG00140.hp2 HG01261.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.454-6298T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996627 | ||||||
| chr9:92996783
|
G | A | 56 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(53): Show | 56 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.454-6142G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996783 | ||||||
| chr9:92996870
|
C | A | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-6055C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996870 | ||||||
| chr9:92996949
|
T | C | 1 | a0001c0002t0004g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.454-5976T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92996949 | ||||||
| chr9:92997159
|
C | T | 1 | a0001c0005t0004g0122 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454-5766C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997159 | ||||||
| chr9:92997379
|
G | A | 1 | a0001c0002t0006g0026 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.454-5546G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997379 | ||||||
| chr9:92997451
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-5474T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997451 | ||||||
| chr9:92997613
|
G | A | 38 | a0001c0001t0001g0057a0001c0001t0001g0270a0001c0001t0001g0271others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.454-5312G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997613 | ||||||
| chr9:92997695
|
T | C | 1 | a0001c0005t0004g0158 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.454-5230T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997695 | ||||||
| chr9:92997844
|
A | C | 1 | a0001c0002t0002g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.454-5081A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997844 | ||||||
| chr9:92997866
|
G | C | 1 | a0008c0025t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.454-5059G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997866 | ||||||
| chr9:92997961
|
C | G | 24 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0281others(21): Show | 24 | HG00408.hp2 HG00673.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.454-4964C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92997961 | ||||||
| chr9:92998174
|
A | G | 4 | a0001c0002t0002g0203a0001c0002t0004g0001a0001c0008t0004g0002others(1): Show | 4 | HG01891.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-4751A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998174 | ||||||
| chr9:92998343
|
C | T | 3 | a0001c0001t0003g0279a0001c0001t0003g0282a0001c0001t0003g0293 | 3 | NA18966.hp2 NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.454-4582C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998343 | ||||||
| chr9:92998406
|
G | A | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-4519G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998406 | ||||||
| chr9:92998480
|
C | A | 1 | a0001c0010t0004g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.454-4445C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998480 | ||||||
| chr9:92998582
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.454-4343C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998582 | ||||||
| chr9:92998699
|
C | T | 1 | a0001c0018t0014g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.454-4226C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998699 | ||||||
| chr9:92998851
|
C | T | 1 | a0001c0002t0002g0233 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.454-4074C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998851 | ||||||
| chr9:92998954
|
C | G | 9 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-3971C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92998954 | ||||||
| chr9:92999024
|
G | A | 1 | a0001c0002t0002g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454-3901G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999024 | ||||||
| chr9:92999098
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-3827C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999098 | ||||||
| chr9:92999139
|
C | A | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-3786C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999139 | ||||||
| chr9:92999173
|
T | C | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-3752T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999173 | ||||||
| chr9:92999284
|
A | G | 3 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0030t0017g0007 | 3 | HG02922.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.454-3641A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999284 | ||||||
| chr9:92999374
|
G | A | 2 | a0001c0004t0001g0068a0001c0004t0001g0069 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.454-3551G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999374 | ||||||
| chr9:92999376
|
C | T | 1 | a0002c0003t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.454-3549C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999376 | ||||||
| chr9:92999386
|
C | T | 13 | a0001c0002t0004g0153a0001c0002t0004g0154a0001c0002t0004g0160others(10): Show | 13 | HG01081.hp1 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.454-3539C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999386 | ||||||
| chr9:92999422
|
G | A | 2 | a0001c0002t0004g0178a0001c0002t0004g0311 | 2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.454-3503G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999422 | ||||||
| chr9:92999589
|
CT | C | 42 | a0001c0001t0001g0126a0001c0001t0001g0141a0001c0001t0001g0144others(39): Show | 42 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.454-3315delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 92999589 | |||||
| chr9:92999620
|
G | A | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-3305G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999620 | ||||||
| chr9:92999668
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.454-3257G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999668 | ||||||
| chr9:92999697
|
G | A | 9 | a0001c0001t0003g0064a0001c0001t0003g0066a0001c0004t0001g0065others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-3228G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999697 | ||||||
| chr9:92999747
|
T | C | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-3178T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999747 | ||||||
| chr9:92999845
|
T | G | 238 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.454-3080T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999845 | ||||||
| chr9:92999883
|
C | T | 10 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-3042C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999883 | ||||||
| chr9:92999884
|
G | A | 27 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.454-3041G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 92999884 | ||||||
| chr9:93000030
|
ATCTT | A | 9 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-2889_454-2886d others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93000030 | |||||
| chr9:93000051
|
A | AT | 205 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.454-2865dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93000051 | |||||
| chr9:93000051
|
A | ATT | 11 | a0001c0001t0001g0144a0001c0001t0005g0011a0001c0001t0005g0014others(8): Show | 11 | HG00323.hp1 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.454-2866_454-2865d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93000051 | |||||
| chr9:93000051
|
A | ATTT | 20 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0005g0013others(17): Show | 20 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.454-2867_454-2865d others(5): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr9 | 93000051 | |||||
| chr9:93000645
|
T | G | 1 | a0001c0002t0002g0195 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.454-2280T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93000645 | ||||||
| chr9:93000914
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.454-2011A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93000914 | ||||||
| chr9:93001345
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.454-1580A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93001345 | ||||||
| chr9:93001426
|
G | A | 1 | a0002c0027t0004g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.454-1499G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93001426 | ||||||
| chr9:93001734
|
G | T | 2 | a0001c0002t0004g0178a0001c0002t0004g0311 | 2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.454-1191G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93001734 | ||||||
| chr9:93001879
|
A | T | 1 | a0001c0001t0003g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.454-1046A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93001879 | ||||||
| chr9:93002303
|
G | T | 1 | a0001c0001t0003g0278 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.454-622G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002303 | ||||||
| chr9:93002341
|
T | G | 1 | a0001c0004t0001g0286 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.454-584T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002341 | ||||||
| chr9:93002355
|
G | A | 27 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.454-570G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002355 | ||||||
| chr9:93002419
|
A | G | 2 | a0001c0005t0004g0005a0001c0005t0004g0006 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.454-506A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002419 | ||||||
| chr9:93002461
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.454-464G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002461 | ||||||
| chr9:93002577
|
G | A | 36 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(33): Show | 36 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.454-348G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002577 | ||||||
| chr9:93002768
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.454-157T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 3/17 | chr9 | 93002768 | ||||||
| chr9:93003090
|
T | C | 1 | a0002c0003t0001g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.543+76T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | chr9 | 93003090 | ||||||
| chr9:93003286
|
G | A | 3 | a0001c0002t0002g0210a0001c0002t0002g0215a0001c0002t0002g0265 | 3 | HG01358.hp1 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.543+272G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | chr9 | 93003286 | ||||||
| chr9:93003425
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+411G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | chr9 | 93003425 | ||||||
| chr9:93003436
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.543+422T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | chr9 | 93003436 | ||||||
| chr9:93003465
|
TGAG | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.543+455_543+457del others(3): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 93003465 | |||||
| chr9:93003473
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+459A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 4/17 | chr9 | 93003473 | ||||||
| chr9:93004149
|
C | T | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.680+12C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004149 | ||||||
| chr9:93004189
|
A | T | 238 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.680+52A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004189 | ||||||
| chr9:93004388
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.680+251A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004388 | ||||||
| chr9:93004400
|
G | C | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.680+263G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004400 | ||||||
| chr9:93004517
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.680+380C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004517 | ||||||
| chr9:93004599
|
G | T | 15 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(12): Show | 15 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.680+462G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004599 | ||||||
| chr9:93004667
|
C | T | 8 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.680+530C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004667 | ||||||
| chr9:93004778
|
C | T | 182 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.680+641C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004778 | ||||||
| chr9:93004797
|
C | T | 1 | a0001c0002t0002g0212 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.680+660C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004797 | ||||||
| chr9:93004799
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.680+662T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93004799 | ||||||
| chr9:93005129
|
A | AT | 12 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(9): Show | 12 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.681-883dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr9 | 93005129 | |||||
| chr9:93005161
|
T | C | 182 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.681-863T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93005161 | ||||||
| chr9:93005280
|
A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.681-744A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93005280 | ||||||
| chr9:93005636
|
A | G | 238 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.681-388A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93005636 | ||||||
| chr9:93005798
|
G | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.681-226G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93005798 | ||||||
| chr9:93005912
|
A | G | 1 | a0001c0002t0002g0246 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.681-112A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 5/17 | chr9 | 93005912 | ||||||
| chr9:93006207
|
A | C | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.837+27A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93006207 | ||||||
| chr9:93007045
|
G | A | 1 | a0001c0001t0011g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.837+865G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007045 | ||||||
| chr9:93007090
|
T | C | 32 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.837+910T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007090 | ||||||
| chr9:93007176
|
C | T | 1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+996C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007176 | ||||||
| chr9:93007231
|
C | T | 79 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(76): Show | 79 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.837+1051C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007231 | ||||||
| chr9:93007239
|
C | T | 1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.837+1059C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007239 | ||||||
| chr9:93007251
|
C | T | 1 | a0001c0008t0004g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837+1071C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007251 | ||||||
| chr9:93007281
|
C | T | 2 | a0001c0001t0001g0221a0006c0022t0001g0220 | 2 | NA19003.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.837+1101C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007281 | ||||||
| chr9:93007463
|
C | T | 1 | a0001c0014t0003g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.837+1283C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007463 | ||||||
| chr9:93007800
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.837+1620C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007800 | ||||||
| chr9:93007879
|
G | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(127): Show | 130 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.837+1699G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007879 | ||||||
| chr9:93007960
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.837+1780G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93007960 | ||||||
| chr9:93008167
|
AT | A | 9 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.837+1988delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008167 | ||||||
| chr9:93008171
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.837+1991C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008171 | ||||||
| chr9:93008279
|
A | G | 1 | a0001c0002t0002g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.838-1967A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008279 | ||||||
| chr9:93008566
|
G | A | 1 | a0001c0002t0002g0234 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.838-1680G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008566 | ||||||
| chr9:93008581
|
G | A | 1 | a0001c0001t0007g0316 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.838-1665G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008581 | ||||||
| chr9:93008627
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.838-1619G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008627 | ||||||
| chr9:93008770
|
T | C | 1 | a0002c0013t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.838-1476T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008770 | ||||||
| chr9:93008962
|
C | CA | 127 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(124): Show | 127 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.838-1269dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr9 | 93008962 | |||||
| chr9:93008991
|
G | A | 8 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.838-1255G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008991 | ||||||
| chr9:93008994
|
A | G | 11 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0001t0007g0315others(8): Show | 11 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.838-1252A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93008994 | ||||||
| chr9:93009211
|
C | T | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.838-1035C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009211 | ||||||
| chr9:93009262
|
C | CA | 174 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(171): Show | 174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.838-972dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr9 | 93009262 | |||||
| chr9:93009287
|
G | T | 35 | a0001c0001t0001g0057a0001c0001t0001g0270a0001c0001t0001g0271others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.838-959G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009287 | ||||||
| chr9:93009294
|
T | A | 1 | a0002c0013t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.838-952T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009294 | ||||||
| chr9:93009361
|
T | A | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.838-885T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009361 | ||||||
| chr9:93009416
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0011g0180 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.838-830T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009416 | ||||||
| chr9:93009512
|
C | T | 4 | a0001c0001t0003g0272a0001c0001t0003g0273a0001c0001t0003g0274others(1): Show | 4 | HG00408.hp2 HG02027.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-734C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009512 | ||||||
| chr9:93009553
|
C | G | 1 | a0005c0028t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.838-693C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009553 | ||||||
| chr9:93009754
|
T | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(175): Show | 178 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.838-492T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009754 | ||||||
| chr9:93009762
|
C | T | 9 | a0001c0002t0002g0312a0001c0002t0004g0115a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-484C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009762 | ||||||
| chr9:93009855
|
G | A | 28 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.838-391G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009855 | ||||||
| chr9:93009925
|
T | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(128): Show | 131 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.838-321T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009925 | ||||||
| chr9:93009946
|
A | G | 238 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.838-300A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009946 | ||||||
| chr9:93009994
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.838-252G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93009994 | ||||||
| chr9:93010040
|
C | T | 1 | a0001c0004t0003g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.838-206C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93010040 | ||||||
| chr9:93010131
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.838-115A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 6/17 | chr9 | 93010131 | ||||||
| chr9:93010443
|
G | T | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.976+59G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010443 | ||||||
| chr9:93010456
|
GGAGA | G | 89 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(86): Show | 89 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.976+80_976+83delAG others(2): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010456 | |||||
| chr9:93010470
|
G | A | 2 | a0001c0001t0009g0084a0001c0002t0002g0312 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.976+86G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010470 | ||||||
| chr9:93010517
|
A | AAGAGAC | 241 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.976+144_976+149dup others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010517 | |||||
| chr9:93010547
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0138 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.976+163A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010547 | ||||||
| chr9:93010567
|
A | G | 3 | a0001c0002t0004g0001a0001c0002t0004g0162a0001c0002t0004g0163 | 3 | HG02615.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.976+183A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010567 | ||||||
| chr9:93010604
|
GGAGAAAC others(57): Show |
G | 1 | a0001c0002t0004g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.976+222_976+285del others(64): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010604 | |||||
| chr9:93010609
|
A | AACAGACG others(62): Show |
1 | a0001c0002t0002g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.976+230_976+231ins others(69): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010609 | |||||
| chr9:93010609
|
A | AACAGAGG others(62): Show |
18 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0139others(15): Show | 18 | HG00323.hp2 HG00639.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.976+281_976+349dup others(69): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010609 | |||||
| chr9:93010609
|
A | AACAGAGG others(131): Show |
5 | a0001c0001t0008g0012a0001c0002t0004g0008a0001c0005t0004g0122others(2): Show | 5 | HG01884.hp1 HG02083.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+349_976+350ins others(138): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010609 | |||||
| chr9:93010609
|
A | AACAGAGG others(200): Show |
3 | a0001c0005t0004g0155a0001c0005t0004g0156a0001c0005t0004g0158 | 3 | HG02630.hp1 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.976+349_976+350ins others(207): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010609 | |||||
| chr9:93010609
|
AACAGAGG others(62): Show |
A | 204 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(201): Show | 204 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+281_976+349del others(69): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010609 | |||||
| chr9:93010620
|
GGAGAGAG others(64): Show |
G | 7 | a0001c0001t0003g0064a0001c0002t0002g0203a0001c0002t0004g0116others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.976+245_976+315del others(71): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010620 | |||||
| chr9:93010629
|
GACACACA others(61): Show |
G | 1 | a0002c0003t0001g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.976+246_976+313del others(68): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010629 | ||||||
| chr9:93010629
|
GACACACA others(64): Show |
G | 1 | a0001c0005t0004g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.976+251_976+321del others(71): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010629 | |||||
| chr9:93010956
|
AGGCAGCC others(2): Show |
A | 33 | a0001c0001t0005g0033a0001c0002t0002g0184a0001c0002t0002g0193others(30): Show | 33 | HG00423.hp1 HG01943.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.977-256_977-248del others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr9 | 93010956 | |||||
| chr9:93010972
|
C | G | 2 | a0001c0001t0001g0141a0001c0001t0005g0037 | 2 | NA18986.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.977-242C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93010972 | ||||||
| chr9:93011178
|
C | T | 1 | a0001c0001t0007g0314 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.977-36C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93011178 | ||||||
| chr9:93011195
|
C | T | 2 | a0001c0009t0003g0289a0001c0009t0003g0290 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.977-19C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93011195 | ||||||
| chr9:93011202
|
T | A | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.977-12T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 7/17 | chr9 | 93011202 | ||||||
| chr9:93011422
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1035+150G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011422 | ||||||
| chr9:93011492
|
C | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0005g0013others(9): Show | 12 | HG00544.hp2 HG02027.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.1035+220C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011492 | ||||||
| chr9:93011595
|
T | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1035+323T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011595 | ||||||
| chr9:93011644
|
T | G | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1035+372T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011644 | ||||||
| chr9:93011855
|
C | CA | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1035+593dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93011855 | |||||
| chr9:93011879
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1035+607C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011879 | ||||||
| chr9:93011934
|
G | T | 4 | a0001c0010t0004g0182a0001c0010t0004g0183a0001c0023t0015g0058others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1035+662G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93011934 | ||||||
| chr9:93012039
|
A | G | 1 | a0001c0004t0001g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1035+767A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012039 | ||||||
| chr9:93012064
|
G | T | 4 | a0001c0002t0004g0153a0001c0002t0004g0164a0001c0002t0004g0178others(1): Show | 4 | HG01081.hp1 HG01952.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1035+792G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012064 | ||||||
| chr9:93012153
|
C | CA | 10 | a0001c0001t0003g0124a0001c0001t0003g0143a0001c0001t0003g0172others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035+899dupA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012153 | |||||
| chr9:93012153
|
CA | C | 17 | a0001c0001t0001g0145a0001c0001t0003g0148a0001c0001t0003g0319others(14): Show | 17 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1035+899delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012153 | |||||
| chr9:93012153
|
CAA | C | 39 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1035+898_1035+899d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012153 | |||||
| chr9:93012153
|
CAAA | C | 96 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(93): Show | 96 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1035+897_1035+899d others(5): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012153 | |||||
| chr9:93012195
|
A | G | 1 | a0001c0004t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1035+923A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012195 | ||||||
| chr9:93012273
|
A | T | 2 | a0001c0001t0005g0034a0001c0001t0013g0030 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1035+1001A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012273 | ||||||
| chr9:93012278
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1035+1006A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012278 | ||||||
| chr9:93012559
|
C | T | 7 | a0001c0004t0001g0065a0001c0004t0001g0068a0001c0004t0001g0069others(4): Show | 7 | HG00639.hp1 HG01074.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035+1287C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012559 | ||||||
| chr9:93012564
|
T | C | 190 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(187): Show | 190 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1036-1288T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012564 | ||||||
| chr9:93012687
|
C | CGGGGGGG others(4): Show |
1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1036-1161_1036-116 others(15): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012687 | |||||
| chr9:93012688
|
G | C | 138 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1036-1164G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012688 | ||||||
| chr9:93012692
|
T | G | 153 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(150): Show | 153 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1036-1160T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012692 | ||||||
| chr9:93012692
|
T | TG | 9 | a0001c0001t0001g0053a0001c0001t0001g0135a0001c0001t0001g0176others(6): Show | 9 | HG00642.hp1 HG00741.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1036-1159dupG | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012692 | |||||
| chr9:93012694
|
T | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(60): Show | 63 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1036-1158T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012694 | ||||||
| chr9:93012695
|
G | T | 31 | a0001c0001t0005g0033a0001c0002t0002g0184a0001c0002t0002g0193others(28): Show | 31 | HG00423.hp1 HG00558.hp2 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.1036-1157G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012695 | ||||||
| chr9:93012697
|
G | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0281others(5): Show | 8 | NA18949.hp2 NA18952.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1036-1155G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012697 | ||||||
| chr9:93012697
|
G | C | 39 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1036-1155G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012697 | ||||||
| chr9:93012697
|
G | T | 1 | a0001c0002t0002g0241 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1036-1155G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012697 | ||||||
| chr9:93012703
|
GA | G | 133 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1036-1147delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 93012703 | |||||
| chr9:93012704
|
A | G | 5 | a0001c0004t0001g0108a0001c0004t0001g0149a0001c0004t0010g0067others(2): Show | 5 | HG00621.hp2 HG01261.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036-1148A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012704 | ||||||
| chr9:93012725
|
G | T | 138 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1036-1127G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012725 | ||||||
| chr9:93012955
|
C | A | 28 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0141others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1036-897C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012955 | ||||||
| chr9:93012997
|
CT | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1036-854delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93012997 | ||||||
| chr9:93013210
|
G | A | 10 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(7): Show | 10 | HG02809.hp2 NA18940.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036-642G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013210 | ||||||
| chr9:93013228
|
C | A | 9 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(6): Show | 9 | NA18940.hp1 NA18962.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036-624C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013228 | ||||||
| chr9:93013279
|
C | T | 28 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0141others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1036-573C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013279 | ||||||
| chr9:93013389
|
G | A | 2 | a0001c0002t0002g0244a0001c0002t0006g0027 | 2 | HG00423.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1036-463G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013389 | ||||||
| chr9:93013433
|
G | A | 28 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0141others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1036-419G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013433 | ||||||
| chr9:93013485
|
C | T | 1 | a0001c0001t0003g0291 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1036-367C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013485 | ||||||
| chr9:93013647
|
G | A | 1 | a0002c0003t0005g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1036-205G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013647 | ||||||
| chr9:93013785
|
C | T | 3 | a0001c0004t0001g0142a0001c0004t0001g0149a0001c0004t0005g0015 | 3 | NA18975.hp1 NA18998.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1036-67C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 8/17 | chr9 | 93013785 | ||||||
| chr9:93014100
|
C | T | 11 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(8): Show | 11 | HG02083.hp1 NA18940.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1182+102C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014100 | ||||||
| chr9:93014259
|
GCC | G | 32 | a0001c0001t0001g0151a0001c0001t0003g0124a0001c0001t0003g0143others(29): Show | 32 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182+263_1182+264d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr9 | 93014259 | |||||
| chr9:93014262
|
C | A | 32 | a0001c0001t0001g0151a0001c0001t0003g0124a0001c0001t0003g0143others(29): Show | 32 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182+264C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014262 | ||||||
| chr9:93014263
|
A | T | 32 | a0001c0001t0001g0151a0001c0001t0003g0124a0001c0001t0003g0143others(29): Show | 32 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182+265A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014263 | ||||||
| chr9:93014359
|
T | C | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1182+361T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014359 | ||||||
| chr9:93014360
|
G | A | 1 | a0001c0002t0004g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1182+362G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014360 | ||||||
| chr9:93014360
|
G | T | 1 | a0001c0004t0005g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1182+362G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014360 | ||||||
| chr9:93014523
|
G | GT | 87 | a0001c0001t0001g0054a0001c0001t0001g0091a0001c0001t0001g0092others(84): Show | 87 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1182+534dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr9 | 93014523 | |||||
| chr9:93014541
|
A | T | 1 | a0006c0022t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1182+543A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014541 | ||||||
| chr9:93014711
|
G | A | 21 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1182+713G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014711 | ||||||
| chr9:93014747
|
T | C | 39 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1182+749T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014747 | ||||||
| chr9:93014862
|
G | A | 11 | a0001c0001t0001g0151a0001c0001t0003g0124a0001c0001t0003g0143others(8): Show | 11 | HG01255.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1182+864G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014862 | ||||||
| chr9:93014888
|
C | A | 1 | a0006c0022t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1183-849C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014888 | ||||||
| chr9:93014889
|
A | C | 1 | a0006c0022t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1183-848A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014889 | ||||||
| chr9:93014928
|
T | A | 6 | a0001c0001t0001g0141a0001c0001t0005g0013a0001c0001t0005g0018others(3): Show | 6 | HG00544.hp2 NA18939.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-809T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93014928 | ||||||
| chr9:93015030
|
C | T | 1 | a0001c0017t0003g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1183-707C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015030 | ||||||
| chr9:93015057
|
C | T | 1 | a0001c0001t0007g0315 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1183-680C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015057 | ||||||
| chr9:93015230
|
C | T | 22 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1183-507C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015230 | ||||||
| chr9:93015312
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(189): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1183-425T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015312 | ||||||
| chr9:93015312
|
T | G | 1 | a0006c0022t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1183-425T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015312 | ||||||
| chr9:93015327
|
C | T | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1183-410C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015327 | ||||||
| chr9:93015413
|
G | A | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1183-324G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015413 | ||||||
| chr9:93015674
|
C | T | 1 | a0005c0028t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1183-63C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015674 | ||||||
| chr9:93015675
|
T | C | 1 | a0005c0028t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1183-62T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015675 | ||||||
| chr9:93015689
|
G | T | 22 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1183-48G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015689 | ||||||
| chr9:93015696
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0002t0004g0115 | 3 | HG02723.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1183-41C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 9/17 | chr9 | 93015696 | ||||||
| chr9:93015833
|
G | C | 21 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1275+4G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93015833 | ||||||
| chr9:93015863
|
C | G | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1275+34C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93015863 | ||||||
| chr9:93016281
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0003g0124a0001c0001t0003g0143others(6): Show | 9 | HG01255.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1275+452C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016281 | ||||||
| chr9:93016335
|
C | CT | 77 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0094others(74): Show | 77 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1275+528dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93016335 | |||||
| chr9:93016335
|
C | CTT | 6 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0001g0152others(3): Show | 6 | HG01175.hp1 HG03669.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+527_1275+528d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93016335 | |||||
| chr9:93016335
|
CT | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0001t0001g0270others(6): Show | 9 | HG01069.hp1 HG01169.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1275+528delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93016335 | |||||
| chr9:93016335
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1275+519_1275+528d others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93016335 | |||||
| chr9:93016362
|
C | T | 1 | a0001c0004t0003g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1275+533C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016362 | ||||||
| chr9:93016369
|
T | TTG | 17 | a0001c0004t0001g0254a0001c0005t0002g0192a0002c0003t0001g0059others(14): Show | 17 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+540_1275+541i others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016369 | ||||||
| chr9:93016371
|
G | GCT | 176 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(173): Show | 176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1275+543_1275+544d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 93016371 | |||||
| chr9:93016371
|
G | T | 17 | a0001c0004t0001g0254a0001c0005t0002g0192a0002c0003t0001g0059others(14): Show | 17 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+542G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016371 | ||||||
| chr9:93016489
|
C | T | 3 | a0001c0001t0007g0313a0001c0001t0011g0317a0001c0002t0002g0246 | 3 | HG02809.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1275+660C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016489 | ||||||
| chr9:93016558
|
G | A | 10 | a0001c0001t0001g0053a0001c0001t0001g0126a0001c0001t0001g0132others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1275+729G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016558 | ||||||
| chr9:93016582
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1275+753C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016582 | ||||||
| chr9:93016632
|
A | T | 22 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1275+803A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016632 | ||||||
| chr9:93016676
|
T | C | 28 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0141others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+847T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016676 | ||||||
| chr9:93016808
|
G | C | 28 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0141others(25): Show | 28 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+979G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016808 | ||||||
| chr9:93016812
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1275+983C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016812 | ||||||
| chr9:93016873
|
G | A | 1 | a0001c0031t0002g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1275+1044G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93016873 | ||||||
| chr9:93017083
|
A | T | 1 | a0006c0022t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1276-1053A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017083 | ||||||
| chr9:93017137
|
G | T | 1 | a0001c0002t0002g0206 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1276-999G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017137 | ||||||
| chr9:93017197
|
G | A | 22 | a0001c0001t0001g0046a0001c0001t0007g0314a0001c0001t0007g0315others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1276-939G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017197 | ||||||
| chr9:93017283
|
T | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0002t0004g0115 | 3 | HG02723.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1276-853T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017283 | ||||||
| chr9:93017460
|
C | T | 1 | a0002c0003t0001g0103 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1276-676C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017460 | ||||||
| chr9:93017537
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1276-599G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017537 | ||||||
| chr9:93017549
|
T | C | 1 | a0005c0028t0002g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1276-587T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017549 | ||||||
| chr9:93017682
|
G | A | 1 | a0002c0003t0001g0079 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1276-454G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017682 | ||||||
| chr9:93017689
|
A | G | 1 | a0002c0003t0003g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1276-447A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017689 | ||||||
| chr9:93017727
|
C | T | 1 | a0001c0001t0003g0302 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1276-409C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017727 | ||||||
| chr9:93017943
|
C | T | 1 | a0001c0002t0004g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1276-193C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017943 | ||||||
| chr9:93017985
|
A | G | 62 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(59): Show | 62 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1276-151A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93017985 | ||||||
| chr9:93018075
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1276-61T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 10/17 | chr9 | 93018075 | ||||||
| chr9:93018288
|
A | G | 21 | a0001c0004t0001g0165a0001c0004t0001g0286a0001c0004t0001g0287others(18): Show | 21 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1355+73A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018288 | ||||||
| chr9:93018627
|
T | C | 7 | a0001c0002t0004g0116a0001c0002t0004g0118a0001c0002t0004g0119others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1355+412T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018627 | ||||||
| chr9:93018753
|
G | A | 38 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1355+538G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018753 | ||||||
| chr9:93018754
|
G | A | 1 | a0002c0003t0001g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1355+539G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018754 | ||||||
| chr9:93018758
|
T | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1355+543T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018758 | ||||||
| chr9:93018796
|
C | A | 38 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1355+581C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018796 | ||||||
| chr9:93018825
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0002t0004g0115 | 3 | HG02723.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1355+610C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018825 | ||||||
| chr9:93018875
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1355+660G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018875 | ||||||
| chr9:93018933
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1355+718C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93018933 | ||||||
| chr9:93019139
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1356-692C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019139 | ||||||
| chr9:93019343
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0251 | 2 | HG01070.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1356-488C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019343 | ||||||
| chr9:93019373
|
C | T | 2 | a0001c0023t0015g0058a0001c0030t0017g0007 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1356-458C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019373 | ||||||
| chr9:93019483
|
G | C | 1 | a0001c0002t0002g0239 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1356-348G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019483 | ||||||
| chr9:93019578
|
A | T | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1356-253A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019578 | ||||||
| chr9:93019744
|
C | A | 1 | a0001c0031t0002g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1356-87C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 11/17 | chr9 | 93019744 | ||||||
| chr9:93019889
|
CA | C | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1386+31delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 93019889 | |||||
| chr9:93020084
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+223G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 12/17 | chr9 | 93020084 | ||||||
| chr9:93020309
|
G | T | 1 | a0001c0002t0002g0190 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.1387-8G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 12/17 | chr9 | 93020309 | ||||||
| chr9:93020466
|
G | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0110a0001c0002t0004g0115 | 3 | HG02723.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1494+42G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020466 | ||||||
| chr9:93020480
|
G | C | 1 | a0001c0002t0002g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1494+56G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020480 | ||||||
| chr9:93020562
|
C | T | 10 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(7): Show | 10 | HG01891.hp2 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1494+138C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020562 | ||||||
| chr9:93020709
|
T | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1494+285T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020709 | ||||||
| chr9:93020716
|
G | T | 2 | a0001c0023t0015g0058a0001c0030t0017g0007 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1494+292G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020716 | ||||||
| chr9:93020794
|
A | G | 1 | a0001c0014t0003g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1494+370A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020794 | ||||||
| chr9:93020809
|
G | A | 82 | a0001c0001t0001g0054a0001c0002t0006g0025a0001c0004t0001g0056others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1494+385G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020809 | ||||||
| chr9:93020876
|
G | T | 104 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0007g0313others(101): Show | 104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1494+452G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020876 | ||||||
| chr9:93020902
|
G | A | 105 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0007g0313others(102): Show | 105 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1494+478G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020902 | ||||||
| chr9:93020911
|
G | A | 1 | a0001c0001t0011g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1494+487G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020911 | ||||||
| chr9:93020941
|
C | T | 11 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(8): Show | 11 | HG02083.hp1 NA18940.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494+517C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93020941 | ||||||
| chr9:93021006
|
A | G | 1 | a0001c0001t0005g0041 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1494+582A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021006 | ||||||
| chr9:93021060
|
G | A | 1 | a0001c0002t0002g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1494+636G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021060 | ||||||
| chr9:93021116
|
G | C | 108 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(105): Show | 108 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1494+692G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021116 | ||||||
| chr9:93021144
|
T | C | 2 | a0001c0023t0015g0058a0001c0030t0017g0007 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1494+720T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021144 | ||||||
| chr9:93021480
|
G | C | 1 | a0001c0001t0011g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1495-847G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021480 | ||||||
| chr9:93021521
|
G | A | 2 | a0001c0023t0015g0058a0001c0030t0017g0007 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1495-806G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021521 | ||||||
| chr9:93021642
|
G | A | 23 | a0001c0001t0001g0046a0001c0001t0007g0313a0001c0001t0007g0314others(20): Show | 23 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1495-685G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021642 | ||||||
| chr9:93021645
|
G | T | 22 | a0001c0001t0001g0046a0001c0001t0007g0313a0001c0001t0007g0314others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1495-682G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021645 | ||||||
| chr9:93021891
|
T | TC | 11 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(8): Show | 11 | HG02083.hp1 NA18940.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495-434dupC | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93021891 | |||||
| chr9:93021934
|
G | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495-393G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93021934 | ||||||
| chr9:93022019
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-308T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93022019 | ||||||
| chr9:93022203
|
A | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(198): Show | 201 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1495-124A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93022203 | ||||||
| chr9:93022213
|
C | T | 38 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0001g0123others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1495-114C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93022213 | ||||||
| chr9:93022227
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1495-100A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93022227 | ||||||
| chr9:93022259
|
T | TC | 19 | a0001c0001t0001g0004a0001c0001t0001g0092a0001c0001t0001g0221others(16): Show | 19 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1495-62dupC | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr9 | 93022259 | |||||
| chr9:93022318
|
C | G | 1 | a0001c0002t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1495-9C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 13/17 | chr9 | 93022318 | ||||||
| chr9:93022570
|
T | C | 19 | a0001c0001t0001g0046a0001c0001t0007g0313a0001c0001t0007g0314others(16): Show | 19 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+181T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93022570 | ||||||
| chr9:93022800
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+411G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93022800 | ||||||
| chr9:93022814
|
C | T | 13 | a0001c0001t0001g0123a0001c0001t0001g0166a0001c0001t0001g0169others(10): Show | 13 | HG02083.hp1 HG03654.hp2 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+425C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93022814 | ||||||
| chr9:93022840
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(9): Show | 12 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+451G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93022840 | ||||||
| chr9:93023022
|
G | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(6): Show | 9 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+633G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023022 | ||||||
| chr9:93023029
|
A | G | 321 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1557+640A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023029 | ||||||
| chr9:93023055
|
T | C | 3 | a0001c0004t0001g0142a0001c0004t0001g0149a0001c0004t0005g0015 | 3 | NA18975.hp1 NA18998.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1557+666T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023055 | ||||||
| chr9:93023107
|
G | A | 25 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(22): Show | 25 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1557+718G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023107 | ||||||
| chr9:93023115
|
C | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(6): Show | 9 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+726C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023115 | ||||||
| chr9:93023118
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1557+729T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023118 | ||||||
| chr9:93023203
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1557+814C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023203 | ||||||
| chr9:93023306
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0138 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1557+917A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023306 | ||||||
| chr9:93023331
|
G | T | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1557+942G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023331 | ||||||
| chr9:93023388
|
C | T | 2 | a0001c0010t0004g0182a0001c0010t0004g0183 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1557+999C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023388 | ||||||
| chr9:93023401
|
C | T | 1 | a0002c0003t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1557+1012C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023401 | ||||||
| chr9:93023473
|
C | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1557+1084C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023473 | ||||||
| chr9:93023537
|
C | T | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1557+1148C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023537 | ||||||
| chr9:93023565
|
G | A | 3 | a0001c0002t0004g0001a0001c0008t0004g0002a0001c0008t0004g0003 | 3 | HG01891.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1557+1176G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023565 | ||||||
| chr9:93023588
|
A | G | 100 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0094others(97): Show | 100 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1557+1199A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023588 | ||||||
| chr9:93023665
|
C | T | 37 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1557+1276C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023665 | ||||||
| chr9:93023783
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1557+1394G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023783 | ||||||
| chr9:93023790
|
A | G | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1557+1401A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023790 | ||||||
| chr9:93023795
|
C | CT | 7 | a0001c0001t0003g0283a0001c0002t0002g0195a0001c0002t0002g0224others(4): Show | 7 | HG01175.hp2 HG02074.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1557+1432dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
C | CTTTTT | 21 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(18): Show | 21 | HG00544.hp2 HG00735.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1557+1428_1557+143 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CT | C | 10 | a0001c0001t0003g0277a0001c0001t0003g0280a0001c0001t0003g0306others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1557+1432delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CTT | C | 14 | a0001c0001t0001g0050a0001c0001t0009g0129a0001c0002t0002g0246others(11): Show | 14 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+1431_1557+143 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CTTT | C | 78 | a0001c0001t0001g0054a0001c0001t0001g0110a0001c0001t0009g0084others(75): Show | 78 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1557+1430_1557+143 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CTTTT | C | 9 | a0001c0001t0001g0094a0001c0001t0007g0313a0001c0001t0007g0314others(6): Show | 9 | HG00323.hp1 HG01168.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+1429_1557+143 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CTTTTTT | C | 10 | a0001c0001t0001g0046a0001c0001t0001g0109a0001c0001t0001g0146others(7): Show | 10 | HG01081.hp1 HG01255.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1557+1427_1557+143 others(10): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023795
|
CTTTTTTT | C | 48 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(45): Show | 48 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1557+1426_1557+143 others(11): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023795 | |||||
| chr9:93023895
|
A | T | 84 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0094others(81): Show | 84 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1557+1506A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93023895 | ||||||
| chr9:93023968
|
AT | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1557+1585delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93023968 | |||||
| chr9:93024044
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1557+1655G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024044 | ||||||
| chr9:93024106
|
C | T | 100 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0094others(97): Show | 100 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1557+1717C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024106 | ||||||
| chr9:93024279
|
C | T | 1 | a0001c0002t0002g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1557+1890C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024279 | ||||||
| chr9:93024296
|
G | T | 1 | a0001c0021t0018g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+1907G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024296 | ||||||
| chr9:93024331
|
G | A | 1 | a0004c0019t0001g0168 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1557+1942G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024331 | ||||||
| chr9:93024451
|
C | T | 9 | a0001c0002t0002g0187a0001c0002t0002g0188a0001c0002t0002g0189others(6): Show | 9 | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+2062C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024451 | ||||||
| chr9:93024475
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1557+2086C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024475 | ||||||
| chr9:93024708
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1557+2319C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024708 | ||||||
| chr9:93024738
|
T | C | 1 | a0001c0001t0009g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557+2349T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024738 | ||||||
| chr9:93024798
|
C | G | 2 | a0001c0001t0011g0317a0001c0002t0002g0246 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1557+2409C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024798 | ||||||
| chr9:93024813
|
T | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1557+2424T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024813 | ||||||
| chr9:93024885
|
C | G | 1 | a0001c0002t0004g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1557+2496C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024885 | ||||||
| chr9:93024928
|
C | T | 48 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(45): Show | 48 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1557+2539C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024928 | ||||||
| chr9:93024964
|
A | G | 2 | a0001c0001t0001g0221a0006c0022t0001g0220 | 2 | NA19003.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1557+2575A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93024964 | ||||||
| chr9:93025023
|
C | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(36): Show | 39 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1557+2634C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025023 | ||||||
| chr9:93025032
|
C | T | 26 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(23): Show | 26 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1557+2643C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025032 | ||||||
| chr9:93025297
|
C | T | 12 | a0001c0001t0009g0084a0001c0001t0009g0129a0001c0002t0004g0116others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+2908C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025297 | ||||||
| chr9:93025350
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1557+2961G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025350 | ||||||
| chr9:93025459
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1557+3070T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025459 | ||||||
| chr9:93025503
|
AGTGT | A | 37 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1557+3116_1557+311 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93025503 | |||||
| chr9:93025717
|
G | A | 13 | a0001c0001t0003g0299a0001c0002t0002g0214a0001c0002t0002g0244others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.1557+3328G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025717 | ||||||
| chr9:93025889
|
G | A | 37 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1557+3500G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025889 | ||||||
| chr9:93025896
|
C | T | 12 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0007g0314others(9): Show | 12 | HG01081.hp1 HG01255.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1557+3507C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025896 | ||||||
| chr9:93025946
|
C | T | 2 | a0001c0001t0011g0317a0001c0002t0002g0246 | 2 | HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1557+3557C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93025946 | ||||||
| chr9:93026341
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1558-3533T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026341 | ||||||
| chr9:93026409
|
G | A | 3 | a0001c0001t0009g0084a0001c0001t0011g0317a0001c0002t0002g0246 | 3 | HG02809.hp2 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1558-3465G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026409 | ||||||
| chr9:93026509
|
C | T | 6 | a0001c0004t0001g0071a0001c0004t0001g0108a0001c0005t0004g0179others(3): Show | 6 | HG02486.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-3365C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026509 | ||||||
| chr9:93026532
|
G | C | 39 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(36): Show | 39 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1558-3342G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026532 | ||||||
| chr9:93026709
|
C | A | 1 | a0007c0024t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1558-3165C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026709 | ||||||
| chr9:93026728
|
C | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(43): Show | 46 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1558-3146C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026728 | ||||||
| chr9:93026739
|
G | C | 74 | a0001c0001t0001g0046a0001c0001t0001g0057a0001c0001t0001g0117others(71): Show | 74 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1558-3135G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026739 | ||||||
| chr9:93026852
|
G | A | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-3022G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026852 | ||||||
| chr9:93026902
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0007g0313others(10): Show | 13 | HG01081.hp1 HG01255.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558-2972G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026902 | ||||||
| chr9:93026911
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1558-2963G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026911 | ||||||
| chr9:93026942
|
C | T | 6 | a0001c0001t0009g0129a0001c0002t0004g0119a0001c0002t0004g0120others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-2932C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93026942 | ||||||
| chr9:93027120
|
C | T | 2 | a0001c0005t0004g0005a0001c0005t0004g0006 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1558-2754C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027120 | ||||||
| chr9:93027146
|
G | C | 1 | a0001c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1558-2728G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027146 | ||||||
| chr9:93027156
|
C | T | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-2718C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027156 | ||||||
| chr9:93027257
|
C | G | 1 | a0001c0002t0004g0245 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1558-2617C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027257 | ||||||
| chr9:93027487
|
G | A | 7 | a0001c0002t0004g0116a0001c0002t0004g0118a0001c0002t0004g0119others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-2387G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027487 | ||||||
| chr9:93027508
|
G | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(197): Show | 200 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1558-2366G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027508 | ||||||
| chr9:93027594
|
C | T | 8 | a0001c0001t0009g0129a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-2280C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027594 | ||||||
| chr9:93027678
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1558-2196C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027678 | ||||||
| chr9:93027715
|
C | CT | 100 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0094others(97): Show | 100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1558-2137dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93027715 | |||||
| chr9:93027715
|
CTTTT | C | 35 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(32): Show | 35 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1558-2140_1558-213 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93027715 | |||||
| chr9:93027715
|
CTTTTT | C | 9 | a0001c0001t0005g0013a0001c0001t0009g0129a0001c0002t0004g0116others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-2141_1558-213 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93027715 | |||||
| chr9:93027715
|
CTTTTTT | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-2142_1558-213 others(10): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93027715 | |||||
| chr9:93027715
|
CTTTTTTT | C | 38 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0125others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1558-2143_1558-213 others(11): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93027715 | |||||
| chr9:93027719
|
T | C | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-2155T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027719 | ||||||
| chr9:93027776
|
A | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(45): Show | 48 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1558-2098A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027776 | ||||||
| chr9:93027781
|
G | A | 25 | a0001c0001t0001g0117a0001c0001t0001g0141a0001c0001t0001g0144others(22): Show | 25 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1558-2093G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027781 | ||||||
| chr9:93027867
|
G | C | 7 | a0001c0002t0002g0184a0001c0002t0002g0243a0001c0002t0002g0249others(4): Show | 7 | HG00423.hp1 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-2007G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027867 | ||||||
| chr9:93027987
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1558-1887G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93027987 | ||||||
| chr9:93028004
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1870C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028004 | ||||||
| chr9:93028009
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1865G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028009 | ||||||
| chr9:93028010
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1864C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028010 | ||||||
| chr9:93028011
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1863G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028011 | ||||||
| chr9:93028012
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1862C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028012 | ||||||
| chr9:93028014
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1860T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028014 | ||||||
| chr9:93028016
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1858G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028016 | ||||||
| chr9:93028017
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1857G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028017 | ||||||
| chr9:93028110
|
A | C | 1 | a0002c0003t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1558-1764A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028110 | ||||||
| chr9:93028122
|
C | T | 1 | a0001c0002t0002g0193 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1558-1752C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028122 | ||||||
| chr9:93028187
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1558-1687C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028187 | ||||||
| chr9:93028197
|
G | GACAC | 4 | a0001c0001t0003g0277a0001c0001t0003g0306a0001c0001t0003g0307others(1): Show | 4 | HG00099.hp1 HG01243.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-1660_1558-165 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028197 | |||||
| chr9:93028197
|
GAC | G | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1558-1658_1558-165 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028197 | |||||
| chr9:93028197
|
GACAC | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(33): Show | 36 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1558-1660_1558-165 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028197 | |||||
| chr9:93028197
|
GACACACA others(15): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1558-1658_1558-163 others(26): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028197 | |||||
| chr9:93028197
|
GACACACA others(19): Show |
G | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1558-1662_1558-163 others(30): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028197 | |||||
| chr9:93028200
|
ACACACAC others(11): Show |
A | 7 | a0001c0002t0004g0116a0001c0002t0004g0118a0001c0002t0004g0119others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-1656_1558-163 others(22): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028200 | |||||
| chr9:93028202
|
A | G | 1 | a0001c0001t0009g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558-1672A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028202 | ||||||
| chr9:93028208
|
ACACACAC others(3): Show |
A | 1 | a0001c0001t0009g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558-1656_1558-164 others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028208 | |||||
| chr9:93028212
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0296 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1558-1657_1558-165 others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028212 | |||||
| chr9:93028212
|
A | ACACG | 44 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1558-1659_1558-165 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028212 | |||||
| chr9:93028214
|
A | ACACACAC others(3): Show |
7 | a0001c0004t0001g0142a0001c0004t0001g0149a0001c0004t0005g0015others(4): Show | 7 | HG00438.hp1 NA18969.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-1657_1558-165 others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028214 | |||||
| chr9:93028214
|
A | ACACACAC others(1): Show |
73 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0057others(70): Show | 73 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1558-1657_1558-165 others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028214 | |||||
| chr9:93028214
|
A | G | 1 | a0001c0002t0004g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1558-1660A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028214 | ||||||
| chr9:93028216
|
A | ACACACG | 6 | a0001c0004t0001g0082a0001c0004t0001g0093a0001c0004t0001g0096others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-1657_1558-165 others(10): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028216 | |||||
| chr9:93028218
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0054others(130): Show | 133 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1558-1656G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028218 | ||||||
| chr9:93028220
|
A | G | 52 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(49): Show | 52 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1558-1654A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028220 | ||||||
| chr9:93028339
|
GA | G | 69 | a0001c0001t0001g0046a0001c0001t0001g0117a0001c0001t0001g0123others(66): Show | 69 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1558-1520delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028339 | |||||
| chr9:93028339
|
GAA | G | 88 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0057others(85): Show | 88 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1558-1521_1558-152 others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028339 | |||||
| chr9:93028350
|
AAAAAG | A | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0109others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-1520_1558-151 others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028350 | |||||
| chr9:93028351
|
AAAAG | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0100others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1558-1515_1558-151 others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028351 | |||||
| chr9:93028448
|
C | T | 1 | a0001c0002t0002g0239 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1558-1426C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028448 | ||||||
| chr9:93028477
|
GTCT | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0007g0313others(10): Show | 13 | HG01081.hp1 HG01255.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558-1392_1558-139 others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028477 | |||||
| chr9:93028542
|
G | A | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1558-1332G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93028542 | ||||||
| chr9:93028995
|
G | GT | 18 | a0001c0001t0003g0124a0001c0001t0003g0272a0001c0001t0003g0274others(15): Show | 18 | HG00423.hp1 HG01175.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1558-837dupT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
G | GTT | 10 | a0001c0001t0003g0089a0001c0002t0002g0209a0001c0002t0002g0214others(7): Show | 10 | HG01069.hp1 HG01515.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-838_1558-837d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
G | GTTTT | 9 | a0001c0001t0003g0066a0001c0001t0003g0173a0001c0002t0002g0250others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558-840_1558-837d others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
G | GTTTTTTT others(6): Show |
1 | a0001c0002t0002g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1558-849_1558-837d others(15): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GT | G | 8 | a0001c0001t0003g0172a0001c0001t0003g0302a0001c0001t0003g0322others(5): Show | 8 | HG00558.hp2 HG02559.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-837delT | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTT | G | 9 | a0001c0001t0003g0280a0001c0001t0003g0282a0001c0001t0003g0284others(6): Show | 9 | HG00639.hp2 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-838_1558-837d others(4): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTT | G | 17 | a0001c0001t0001g0053a0001c0001t0001g0128a0001c0001t0001g0132others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1558-839_1558-837d others(5): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTT | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0126a0001c0001t0001g0135others(12): Show | 15 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-840_1558-837d others(6): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTT | G | 14 | a0001c0001t0001g0100a0001c0001t0001g0125a0001c0001t0001g0127others(11): Show | 14 | HG00609.hp1 HG01070.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-841_1558-837d others(7): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTT | G | 11 | a0001c0001t0001g0092a0001c0002t0002g0255a0001c0002t0004g0311others(8): Show | 11 | HG00408.hp1 HG00673.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558-842_1558-837d others(8): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT | G | 19 | a0001c0001t0001g0057a0001c0001t0001g0091a0001c0001t0001g0109others(16): Show | 19 | HG00423.hp2 HG00558.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1558-843_1558-837d others(9): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(1): Show |
G | 16 | a0001c0001t0001g0300a0001c0001t0003g0299a0001c0002t0004g0162others(13): Show | 16 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1558-844_1558-837d others(10): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(2): Show |
G | 33 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0151others(30): Show | 33 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1558-845_1558-837d others(11): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(3): Show |
G | 51 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0110others(48): Show | 51 | HG00544.hp1 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1558-846_1558-837d others(12): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(4): Show |
G | 27 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0144others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1558-847_1558-837d others(13): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0003g0278a0001c0001t0011g0317a0001c0002t0002g0246others(1): Show | 4 | HG02809.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-848_1558-837d others(14): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(6): Show |
G | 4 | a0001c0001t0009g0129a0001c0001t0011g0180a0001c0004t0010g0062others(1): Show | 4 | HG01261.hp1 HG01975.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-849_1558-837d others(15): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(7): Show |
G | 10 | a0001c0002t0002g0188a0001c0002t0002g0189a0001c0002t0002g0190others(7): Show | 10 | HG00642.hp2 HG01123.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-850_1558-837d others(16): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(8): Show |
G | 4 | a0001c0002t0002g0187a0001c0002t0002g0204a0001c0002t0004g0120others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-851_1558-837d others(17): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(11): Show |
G | 3 | a0001c0001t0001g0170a0001c0002t0002g0228a0001c0002t0002g0230 | 3 | NA18965.hp1 NA18965.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1558-854_1558-837d others(20): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0002t0004g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1558-855_1558-837d others(21): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(13): Show |
G | 2 | a0001c0009t0003g0289a0001c0009t0003g0290 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1558-856_1558-837d others(22): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(15): Show |
G | 1 | a0001c0004t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1558-858_1558-837d others(24): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(18): Show |
G | 1 | a0001c0002t0002g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1558-861_1558-837d others(27): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93028995
|
GTTTTTTT others(20): Show |
G | 3 | a0001c0001t0003g0319a0001c0004t0001g0142a0001c0004t0005g0015 | 3 | NA18977.hp2 NA18998.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1558-863_1558-837d others(29): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 93028995 | |||||
| chr9:93029002
|
T | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0128a0001c0001t0001g0132others(5): Show | 8 | HG00741.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-872T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029002 | ||||||
| chr9:93029003
|
T | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0126a0001c0001t0001g0135others(11): Show | 14 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-871T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029003 | ||||||
| chr9:93029004
|
T | G | 14 | a0001c0001t0001g0100a0001c0001t0001g0125a0001c0001t0001g0127others(11): Show | 14 | HG00609.hp1 HG01070.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-870T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029004 | ||||||
| chr9:93029005
|
T | G | 2 | a0001c0001t0001g0092a0001c0002t0004g0311 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1558-869T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029005 | ||||||
| chr9:93029006
|
T | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0007g0316others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-868T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029006 | ||||||
| chr9:93029008
|
T | G | 3 | a0001c0001t0001g0221a0001c0014t0003g0049a0006c0022t0001g0220 | 3 | HG03834.hp1 NA19003.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1558-866T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029008 | ||||||
| chr9:93029015
|
T | G | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-859T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029015 | ||||||
| chr9:93029018
|
T | G | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-856T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029018 | ||||||
| chr9:93029019
|
T | G | 1 | a0001c0004t0001g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1558-855T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029019 | ||||||
| chr9:93029020
|
T | G | 5 | a0001c0002t0004g0116a0001c0002t0004g0118a0001c0002t0004g0119others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-854T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029020 | ||||||
| chr9:93029021
|
T | G | 3 | a0001c0001t0009g0084a0001c0002t0004g0120a0001c0002t0004g0121 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1558-853T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029021 | ||||||
| chr9:93029023
|
T | G | 2 | a0001c0004t0001g0098a0001c0004t0001g0099 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1558-851T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029023 | ||||||
| chr9:93029024
|
T | G | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-850T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029024 | ||||||
| chr9:93029042
|
C | T | 1 | a0001c0004t0001g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1558-832C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029042 | ||||||
| chr9:93029046
|
A | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0091others(44): Show | 47 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1558-828A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029046 | ||||||
| chr9:93029071
|
G | T | 1 | a0001c0004t0010g0062 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1558-803G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029071 | ||||||
| chr9:93029457
|
G | A | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1558-417G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029457 | ||||||
| chr9:93029610
|
T | C | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1558-264T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029610 | ||||||
| chr9:93029688
|
G | A | 1 | a0001c0001t0003g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1558-186G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029688 | ||||||
| chr9:93029813
|
C | T | 2 | a0001c0002t0002g0210a0001c0002t0002g0215 | 2 | HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1558-61C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 14/17 | chr9 | 93029813 | ||||||
| chr9:93030106
|
C | T | 8 | a0001c0001t0009g0129a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+110C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030106 | ||||||
| chr9:93030160
|
T | G | 1 | a0001c0002t0002g0190 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1680+164T>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030160 | ||||||
| chr9:93030170
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0313a0001c0001t0007g0314others(1): Show | 4 | HG01255.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1680+174G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030170 | ||||||
| chr9:93030383
|
G | A | 1 | a0001c0001t0003g0303 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1680+387G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030383 | ||||||
| chr9:93030445
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0005g0034a0001c0001t0005g0041others(1): Show | 4 | HG00323.hp2 HG00735.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680+449C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030445 | ||||||
| chr9:93030502
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0313a0001c0001t0007g0314others(1): Show | 4 | HG01255.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1680+506G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030502 | ||||||
| chr9:93030631
|
G | T | 1 | a0002c0003t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1680+635G>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030631 | ||||||
| chr9:93030707
|
C | CG | 13 | a0001c0001t0001g0050a0001c0001t0001g0140a0001c0001t0001g0169others(10): Show | 13 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1680+718dupG | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | 93030707 | |||||
| chr9:93030713
|
G | A | 6 | a0001c0001t0003g0124a0001c0001t0003g0143a0001c0001t0011g0180others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1680+717G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030713 | ||||||
| chr9:93030718
|
CA | C | 115 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0057others(112): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1680+723delA | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030718 | ||||||
| chr9:93030719
|
A | G | 8 | a0001c0001t0005g0032a0001c0002t0004g0216a0001c0002t0004g0248others(5): Show | 8 | HG00741.hp2 HG02056.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1680+723A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030719 | ||||||
| chr9:93030722
|
G | C | 1 | a0001c0004t0001g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1680+726G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030722 | ||||||
| chr9:93030725
|
G | A | 2 | a0001c0004t0010g0062a0001c0004t0010g0067 | 2 | HG01261.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1680+729G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030725 | ||||||
| chr9:93030865
|
G | A | 3 | a0001c0001t0003g0124a0001c0001t0003g0143a0001c0016t0003g0171 | 3 | HG02145.hp1 HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1680+869G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93030865 | ||||||
| chr9:93031352
|
G | A | 8 | a0001c0001t0009g0129a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+1356G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031352 | ||||||
| chr9:93031512
|
C | T | 1 | a0001c0002t0002g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1681-1257C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031512 | ||||||
| chr9:93031519
|
C | T | 2 | a0001c0009t0003g0289a0001c0009t0003g0290 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1681-1250C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031519 | ||||||
| chr9:93031534
|
A | G | 85 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0094others(82): Show | 85 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1681-1235A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031534 | ||||||
| chr9:93031576
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1681-1193C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031576 | ||||||
| chr9:93031660
|
G | A | 18 | a0001c0001t0003g0172a0001c0001t0003g0273a0001c0001t0003g0275others(15): Show | 18 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1681-1109G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031660 | ||||||
| chr9:93031789
|
A | T | 71 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(68): Show | 71 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1681-980A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031789 | ||||||
| chr9:93031986
|
A | C | 1 | a0002c0003t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1681-783A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93031986 | ||||||
| chr9:93032100
|
T | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(68): Show | 71 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1681-669T>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93032100 | ||||||
| chr9:93032104
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(65): Show | 68 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1681-665G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93032104 | ||||||
| chr9:93032111
|
A | G | 71 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(68): Show | 71 | HG00099.hp2 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1681-658A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93032111 | ||||||
| chr9:93032597
|
C | T | 1 | a0001c0018t0014g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1681-172C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93032597 | ||||||
| chr9:93032619
|
A | G | 6 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0007g0316others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1681-150A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | chr9 | 93032619 | ||||||
| chr9:93032664
|
TCCTCCCG others(9): Show |
T | 85 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0094others(82): Show | 85 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1681-90_1681-75del others(16): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | 93032664 | |||||
| chr9:93032910
|
G | A | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1785+37G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93032910 | ||||||
| chr9:93032945
|
A | G | 14 | a0001c0004t0001g0254a0002c0003t0001g0059a0002c0003t0001g0073others(11): Show | 14 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1785+72A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93032945 | ||||||
| chr9:93032969
|
C | T | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1785+96C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93032969 | ||||||
| chr9:93033279
|
C | T | 2 | a0001c0004t0001g0112a0001c0004t0001g0113 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1785+406C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033279 | ||||||
| chr9:93033281
|
C | CCTCCTCC others(16): Show |
1 | a0001c0005t0002g0192 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1785+461_1785+483d others(25): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033281 | |||||
| chr9:93033281
|
CCTCCTCC others(16): Show |
C | 92 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0094others(89): Show | 92 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1785+461_1785+483d others(25): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033281 | |||||
| chr9:93033282
|
C | T | 1 | a0001c0002t0002g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1785+409C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033282 | ||||||
| chr9:93033293
|
CCCCGTCC others(15): Show |
C | 1 | a0001c0002t0004g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1785+424_1785+445d others(24): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033293 | |||||
| chr9:93033297
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1785+424G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033297 | ||||||
| chr9:93033326
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1785+453T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033326 | ||||||
| chr9:93033327
|
TCTC | T | 53 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0053others(50): Show | 53 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1785+465_1785+467d others(5): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033327 | |||||
| chr9:93033330
|
C | CCTCCTCC others(33): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0125others(9): Show | 12 | HG00609.hp1 HG01070.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1785+464_1785+465i others(42): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033330 | |||||
| chr9:93033330
|
C | CCTCCTCC others(13): Show |
2 | a0001c0008t0004g0002a0001c0008t0004g0003 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1785+464_1785+483d others(22): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033330 | |||||
| chr9:93033339
|
C | A | 6 | a0001c0001t0003g0148a0001c0002t0002g0226a0001c0002t0002g0227others(3): Show | 6 | HG01943.hp1 NA18946.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1785+466C>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033339 | ||||||
| chr9:93033343
|
G | C | 21 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0151others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1785+470G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033343 | ||||||
| chr9:93033355
|
T | TCTTCCTC others(6): Show |
37 | a0001c0001t0001g0117a0001c0001t0001g0123a0001c0001t0001g0141others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1785+497_1785+509d others(15): Show |
FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | 93033355 | |||||
| chr9:93033358
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1785+485T>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033358 | ||||||
| chr9:93033426
|
C | T | 3 | a0001c0021t0018g0181a0001c0023t0015g0058a0001c0030t0017g0007 | 3 | HG02258.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1785+553C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033426 | ||||||
| chr9:93033439
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1785+566G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033439 | ||||||
| chr9:93033577
|
A | C | 194 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1785+704A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033577 | ||||||
| chr9:93033711
|
G | A | 2 | a0001c0002t0006g0021a0001c0002t0006g0024 | 2 | NA18971.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1786-830G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033711 | ||||||
| chr9:93033781
|
A | C | 8 | a0001c0001t0009g0129a0001c0002t0004g0116a0001c0002t0004g0118others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1786-760A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033781 | ||||||
| chr9:93033830
|
C | T | 1 | a0001c0020t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1786-711C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033830 | ||||||
| chr9:93033835
|
A | G | 1 | a0001c0001t0009g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1786-706A>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033835 | ||||||
| chr9:93033869
|
A | T | 1 | a0001c0001t0003g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1786-672A>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93033869 | ||||||
| chr9:93034147
|
G | C | 3 | a0001c0001t0011g0317a0001c0002t0002g0246a0001c0002t0002g0312 | 3 | HG02809.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1786-394G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 16/17 | chr9 | 93034147 | ||||||
| chr9:93034776
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1926+95A>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/17 | chr9 | 93034776 | ||||||
| chr9:93034799
|
G | C | 1 | a0001c0001t0003g0293 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1926+118G>C | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/17 | chr9 | 93034799 | ||||||
| chr9:93034815
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(189): Show | 192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1926+134G>A | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/17 | chr9 | 93034815 | ||||||
| chr9:93034924
|
C | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0050others(104): Show | 107 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1926+243C>G | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/17 | chr9 | 93034924 | ||||||
| chr9:93035164
|
C | T | 123 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0094others(120): Show | 123 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1927-174C>T | FGD3 | ENSG00000127084.19 | transcript | ENST00000375482.8 | protein_coding | 17/17 | chr9 | 93035164 |