Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83856 |
|---|---|
| ensemblid | ENSG00000106701.13 |
| hgncid | 13753 |
| symbol | FSD1L |
| name | fibronectin type III and SPRY domain containing 1 like |
| refseq_nuc | NM_001145313.3 |
| refseq_prot | NP_001138785.1 |
| ensembl_nuc | ENST00000481272.6 |
| ensembl_prot | ENSP00000417492.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 105448034 |
| end | 105552433 |
| strand | + |
| ver | v1.2 |
| region | chr9:105448034-105552433 |
| region5000 | chr9:105443034-105557433 |
| regionname0 | FSD1L_chr9_105448034_105552433 |
| regionname5000 | FSD1L_chr9_105443034_105557433 |
| 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 | 530 | 377 | 89 | 63 | 180 | 13 | 30 | 142 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0002 | 0/0 | 530 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0003 | 0/0 | 530 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1593 | 369 | 83 | 63 | 178 | 13 | 30 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| c0002 | 0/0 | 1593 | 6 | 6 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| c0003 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| c0004 | 0/0 | 1593 | 2 | 0 | 1 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| c0005 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 6138 | 89 | 15 | 16 | 48 | 0 | 9 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0002 | 0/0 | 6141 | 79 | 1 | 10 | 64 | 0 | 4 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0003 | 0/0 | 6140 | 42 | 1 | 8 | 26 | 3 | 4 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0004 | 0/1 | 6147 | 42 | 17 | 12 | 8 | 2 | 2 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0005 | 0/0 | 6138 | 33 | 16 | 7 | 0 | 3 | 7 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0006 | 0/0 | 6140 | 9 | 0 | 3 | 6 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0007 | 0/0 | 6140 | 8 | 8 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0008 | 0/0 | 6138 | 8 | 0 | 0 | 8 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0009 | 0/0 | 6141 | 6 | 1 | 3 | 0 | 2 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0010 | 0/0 | 6148 | 5 | 4 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0011 | 0/0 | 6129 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0012 | 0/0 | 6140 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0013 | 0/0 | 6140 | 4 | 3 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0014 | 0/0 | 6138 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0015 | 0/0 | 6140 | 4 | 0 | 0 | 4 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0016 | 0/0 | 6141 | 3 | 0 | 0 | 3 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0017 | 0/0 | 6138 | 3 | 1 | 0 | 0 | 2 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0018 | 0/0 | 6140 | 2 | 0 | 0 | 0 | 0 | 2 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0019 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0020 | 0/0 | 6140 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0021 | 0/0 | 6140 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0022 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0023 | 0/0 | 6141 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0024 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0025 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0026 | 0/0 | 6141 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0027 | 0/0 | 6141 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0028 | 0/0 | 6141 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0029 | 0/0 | 6141 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0030 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0031 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0032 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0033 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0034 | 0/0 | 6141 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0035 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0036 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0037 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0038 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0039 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0040 | 0/0 | 6148 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0041 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0042 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| t0043 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1593 | 369 | 83 | 63 | 178 | 13 | 30 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0002 | 0/0 | 1593 | 6 | 6 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0003 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0002c0004 | 0/0 | 1593 | 2 | 0 | 1 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0003c0005 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7730 | 89 | 15 | 16 | 48 | 0 | 9 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0002 | 0/0 | 7733 | 78 | 1 | 9 | 64 | 0 | 4 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0003 | 0/0 | 7732 | 40 | 1 | 8 | 24 | 3 | 4 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0004 | 0/1 | 7739 | 42 | 17 | 12 | 8 | 2 | 2 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0005 | 0/0 | 7730 | 33 | 16 | 7 | 0 | 3 | 7 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0006 | 0/0 | 7732 | 9 | 0 | 3 | 6 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0007 | 0/0 | 7732 | 8 | 8 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0008 | 0/0 | 7730 | 8 | 0 | 0 | 8 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0009 | 0/0 | 7733 | 6 | 1 | 3 | 0 | 2 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0010 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0011 | 0/0 | 7721 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0012 | 0/0 | 7732 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0013 | 0/0 | 7732 | 4 | 3 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0014 | 0/0 | 7730 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0015 | 0/0 | 7732 | 4 | 0 | 0 | 4 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0016 | 0/0 | 7733 | 3 | 0 | 0 | 3 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0017 | 0/0 | 7730 | 3 | 1 | 0 | 0 | 2 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0018 | 0/0 | 7732 | 2 | 0 | 0 | 0 | 0 | 2 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0019 | 0/0 | 7730 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0020 | 0/0 | 7732 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0022 | 0/0 | 7730 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0023 | 0/0 | 7733 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0024 | 0/0 | 7730 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0025 | 0/0 | 7730 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0026 | 0/0 | 7733 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0027 | 0/0 | 7733 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0028 | 0/0 | 7733 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0030 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0031 | 0/0 | 7732 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0032 | 0/0 | 7730 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0033 | 0/0 | 7730 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0035 | 0/0 | 7730 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0036 | 0/0 | 7732 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0037 | 0/0 | 7730 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0038 | 0/0 | 7730 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0039 | 0/0 | 7730 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0040 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0041 | 0/0 | 7739 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0042 | 0/0 | 7739 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0001t0043 | 0/0 | 7730 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0002t0010 | 0/0 | 7740 | 4 | 4 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0002t0021 | 0/0 | 7732 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0001c0003t0003 | 0/0 | 7732 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0002c0004t0002 | 0/0 | 7733 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0002c0004t0029 | 0/0 | 7733 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| a0003c0005t0034 | 0/0 | 7733 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | copy fasta | chr9 | 105443034 | 105557433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0004g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0006g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0014g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0015g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0015g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0015g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0015g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0016g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0017g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0018g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0018g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0019g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0020g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0020g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0022g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0023g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0023g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0024g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0025g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0026g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0027g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0028g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0030g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0031g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0032g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0033g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0035g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0036g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0037g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0038g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0039g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0040g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0041g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0042g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0001t0043g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0021g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0002t0021g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0003t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0001c0003t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0002c0004t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0002c0004t0029g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| a0003c0005t0034g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0115 | EUR | GBR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00099 | hp2 | a0001 | c0001 | t0017 | g0244 | EUR | GBR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0169 | EUR | GBR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00140 | hp2 | a0002 | c0004 | t0029 | g0074 | EUR | GBR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0175 | EUR | FIN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00280 | hp2 | a0001 | c0001 | t0017 | g0226 | EUR | FIN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0343 | EUR | FIN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0197 | EUR | FIN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00408 | hp1 | a0001 | c0001 | t0024 | g0254 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00438 | hp1 | a0001 | c0001 | t0043 | g0269 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0365 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00609 | hp2 | a0001 | c0001 | t0023 | g0319 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00642 | hp2 | a0001 | c0001 | t0025 | g0227 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0167 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01074 | hp2 | a0001 | c0001 | t0010 | g0108 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0190 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01109 | hp1 | a0002 | c0004 | t0002 | g0016 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0096 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0372 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0373 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0193 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0341 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01361 | hp2 | a0001 | c0001 | t0020 | g0368 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0370 | EUR | IBS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01515 | hp2 | a0001 | c0001 | t0037 | g0154 | EUR | IBS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0112 | EUR | IBS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0371 | EUR | IBS | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0098 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01934 | hp2 | a0001 | c0001 | t0020 | g0369 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0361 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0245 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0360 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0374 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CDX | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0334 | EAS | CDX | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02165 | hp1 | a0001 | c0001 | t0024 | g0255 | EAS | CDX | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0097 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0110 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0364 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0346 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02451 | hp2 | a0001 | c0002 | t0010 | g0137 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0170 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0224 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02622 | hp1 | a0001 | c0001 | t0041 | g0118 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0315 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02735 | hp2 | a0001 | c0001 | t0018 | g0330 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02818 | hp2 | a0001 | c0001 | t0012 | g0099 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02896 | hp2 | a0001 | c0001 | t0031 | g0192 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02965 | hp2 | a0001 | c0001 | t0022 | g0173 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0122 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0207 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0095 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03098 | hp2 | a0001 | c0002 | t0021 | g0316 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03130 | hp1 | a0001 | c0002 | t0021 | g0317 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0211 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0189 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0188 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0313 | AFR | ESN | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03540 | hp2 | a0003 | c0005 | t0034 | g0149 | AFR | GWD | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03579 | hp1 | a0001 | c0001 | t0040 | g0223 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0157 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0172 | SAS | STU | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0329 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0168 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0171 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0322 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0375 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG04228 | hp1 | a0001 | c0001 | t0027 | g0080 | SAS | STU | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18522 | hp1 | a0001 | c0001 | t0032 | g0163 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18612 | hp2 | a0001 | c0001 | t0028 | g0069 | EAS | CHB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18906 | hp1 | a0001 | c0001 | t0030 | g0152 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0347 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18949 | hp1 | a0001 | c0001 | t0008 | g0301 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0333 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18954 | hp1 | a0001 | c0001 | t0019 | g0294 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18957 | hp1 | a0001 | c0001 | t0008 | g0296 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18959 | hp2 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18961 | hp2 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0348 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18972 | hp2 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18973 | hp2 | a0001 | c0001 | t0015 | g0327 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18977 | hp1 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18980 | hp1 | a0001 | c0001 | t0015 | g0328 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18984 | hp1 | a0001 | c0001 | t0015 | g0326 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18984 | hp2 | a0001 | c0001 | t0035 | g0232 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0332 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18993 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18995 | hp2 | a0001 | c0001 | t0019 | g0258 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18998 | hp1 | a0001 | c0001 | t0036 | g0359 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18999 | hp1 | a0001 | c0001 | t0026 | g0012 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19006 | hp1 | a0001 | c0001 | t0015 | g0340 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0297 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0345 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0344 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19043 | hp1 | a0001 | c0001 | t0042 | g0147 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19058 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19058 | hp2 | a0001 | c0001 | t0023 | g0339 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19060 | hp2 | a0001 | c0001 | t0039 | g0279 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19086 | hp2 | a0001 | c0001 | t0038 | g0282 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0304 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0206 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | YRI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ASW | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0191 | EUR | TSI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0161 | EUR | TSI | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | GIH | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20905 | hp2 | a0001 | c0001 | t0033 | g0155 | SAS | GIH | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02109 | hp2 | a0001 | c0002 | t0010 | g0105 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0321 | AFR | ACB | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0314 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0094 | AFR | MSL | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | USA | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | USA | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | USA | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | USA | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | LWK | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0203 | REF | REF | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0293 | REF | REF | FSD1L_chr9_105443034_105557433 | FSD1L | chr9 | 105443034 | 105557433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105471926
|
A | G | 1 | a0002 | 2 | HG00140.hp2 HG01109.hp1 |
missense_variant | MODERATE | c.362A>G | p.Asn121Ser | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/14 | 549/7730 | 362/1593 | 121/530 | chr9 | 105471926 | ||
| chr9:105471961
|
G | T | 1 | a0003 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.397G>T | p.Ala133Ser | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/14 | 584/7730 | 397/1593 | 133/530 | chr9 | 105471961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105471972
|
A | G | 1 | a0001c0002 | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
synonymous_variant | LOW | c.408A>G | p.Ser136Ser | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/14 | 595/7730 | 408/1593 | 136/530 | chr9 | 105471972 | ||
| chr9:105534505
|
A | G | 1 | a0001c0003 | 2 | NA18952.hp1 NA18989.hp1 |
synonymous_variant | LOW | c.1038A>G | p.Pro346Pro | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/14 | 1225/7730 | 1038/1593 | 346/530 | chr9 | 105534505 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105448050
|
C | A | 1 | a0001c0001t0018 | 2 | HG02735.hp2 HG03704.hp1 |
5_prime_UTR_variant | MODIFIER | c.-171C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/14 | 171 | chr9 | 105448050 | |||||
| chr9:105448107
|
C | T | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-114C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/14 | chr9 | 105448107 | ||||||
| chr9:105448153
|
G | C | 1 | a0001c0001t0025 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-68G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/14 | 68 | chr9 | 105448153 | |||||
| chr9:105546769
|
ACTTTGAC others(4): Show |
A | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*289_*299delTTGACT others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 289 | INFO_REALIGN_3_PRIME | chr9 | 105546769 | ||||
| chr9:105546908
|
G | A | 1 | a0001c0001t0018 | 2 | HG02735.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*425G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 425 | chr9 | 105546908 | |||||
| chr9:105547065
|
T | C | 1 | a0001c0001t0012 | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*582T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 582 | chr9 | 105547065 | |||||
| chr9:105547132
|
C | T | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*649C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 649 | chr9 | 105547132 | |||||
| chr9:105547139
|
T | TA | 7 | a0001c0001t0002a0001c0001t0016a0001c0001t0026others(4): Show | 86 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*657dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 658 | INFO_REALIGN_3_PRIME | chr9 | 105547139 | ||||
| chr9:105547152
|
A | G | 1 | a0001c0001t0042 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*669A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 669 | chr9 | 105547152 | |||||
| chr9:105547161
|
G | C | 1 | a0001c0001t0019 | 2 | NA18954.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*678G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 678 | chr9 | 105547161 | |||||
| chr9:105547292
|
T | TGTGTTTG | 6 | a0001c0001t0004a0001c0001t0010a0001c0001t0040others(3): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*812_*818dupGTTTGG others(1): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 819 | INFO_REALIGN_3_PRIME | chr9 | 105547292 | ||||
| chr9:105547327
|
G | A | 1 | a0001c0001t0009 | 6 | HG00323.hp2 HG01106.hp1 HG01255.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*844G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 844 | chr9 | 105547327 | |||||
| chr9:105547370
|
A | G | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*887A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 887 | chr9 | 105547370 | |||||
| chr9:105547571
|
C | T | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1088C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1088 | chr9 | 105547571 | |||||
| chr9:105547587
|
T | G | 2 | a0001c0001t0012a0001c0001t0013 | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1104T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1104 | chr9 | 105547587 | |||||
| chr9:105547648
|
A | T | 1 | a0001c0001t0013 | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1165A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1165 | chr9 | 105547648 | |||||
| chr9:105547684
|
A | G | 1 | a0001c0001t0008 | 8 | NA18949.hp1 NA18957.hp1 NA18959.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1201A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1201 | chr9 | 105547684 | |||||
| chr9:105547697
|
T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1214T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1214 | chr9 | 105547697 | |||||
| chr9:105548013
|
T | G | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1530T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1530 | chr9 | 105548013 | |||||
| chr9:105548353
|
G | A | 1 | a0001c0001t0032 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1870G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1870 | chr9 | 105548353 | |||||
| chr9:105548421
|
C | A | 3 | a0001c0001t0005a0001c0001t0030a0001c0001t0033 | 35 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1938C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 1938 | chr9 | 105548421 | |||||
| chr9:105548718
|
A | G | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2235A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2235 | chr9 | 105548718 | |||||
| chr9:105548769
|
T | C | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2286T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2286 | chr9 | 105548769 | |||||
| chr9:105548831
|
G | C | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2348 | chr9 | 105548831 | |||||
| chr9:105549121
|
G | A | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2638G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2638 | chr9 | 105549121 | |||||
| chr9:105549151
|
C | T | 1 | a0001c0001t0015 | 4 | NA18973.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2668C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2668 | chr9 | 105549151 | |||||
| chr9:105549228
|
A | G | 1 | a0001c0001t0039 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2745A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2745 | chr9 | 105549228 | |||||
| chr9:105549272
|
G | A | 1 | a0003c0005t0034 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2789G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2789 | chr9 | 105549272 | |||||
| chr9:105549272
|
G | C | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2789G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 2789 | chr9 | 105549272 | |||||
| chr9:105549483
|
A | T | 1 | a0001c0001t0038 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3000A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3000 | chr9 | 105549483 | |||||
| chr9:105549484
|
C | A | 1 | a0001c0001t0038 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3001C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3001 | chr9 | 105549484 | |||||
| chr9:105549877
|
A | T | 5 | a0001c0001t0004a0001c0001t0010a0001c0001t0041others(2): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3394A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3394 | chr9 | 105549877 | |||||
| chr9:105549907
|
A | C | 1 | a0001c0001t0017 | 3 | HG00099.hp2 HG00280.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3424A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3424 | chr9 | 105549907 | |||||
| chr9:105549916
|
T | C | 1 | a0003c0005t0034 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3433T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3433 | chr9 | 105549916 | |||||
| chr9:105550008
|
C | T | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3525C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3525 | chr9 | 105550008 | |||||
| chr9:105550009
|
G | A | 1 | a0001c0001t0020 | 2 | HG01361.hp2 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3526G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3526 | chr9 | 105550009 | |||||
| chr9:105550035
|
C | A | 1 | a0001c0001t0033 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3552C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3552 | chr9 | 105550035 | |||||
| chr9:105550198
|
T | A | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3715T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3715 | chr9 | 105550198 | |||||
| chr9:105550318
|
T | C | 1 | a0001c0001t0041 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3835T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3835 | chr9 | 105550318 | |||||
| chr9:105550408
|
G | A | 1 | a0001c0002t0021 | 2 | HG03098.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3925G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3925 | chr9 | 105550408 | |||||
| chr9:105550453
|
G | A | 1 | a0001c0001t0014 | 4 | HG02615.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3970G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 3970 | chr9 | 105550453 | |||||
| chr9:105550596
|
T | C | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4113T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4113 | chr9 | 105550596 | |||||
| chr9:105550618
|
A | G | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(7): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4135A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4135 | chr9 | 105550618 | |||||
| chr9:105550683
|
C | T | 1 | a0001c0001t0006 | 9 | HG01261.hp2 HG02148.hp2 HG02155.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4200C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4200 | chr9 | 105550683 | |||||
| chr9:105550712
|
C | G | 1 | a0002c0004t0029 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4229C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4229 | chr9 | 105550712 | |||||
| chr9:105550935
|
A | T | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4452A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4452 | chr9 | 105550935 | |||||
| chr9:105551012
|
A | G | 1 | a0001c0001t0024 | 2 | HG00408.hp1 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4529A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4529 | chr9 | 105551012 | |||||
| chr9:105551090
|
A | C | 1 | a0001c0001t0011 | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4607A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4607 | chr9 | 105551090 | |||||
| chr9:105551256
|
C | T | 1 | a0001c0001t0028 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4773C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4773 | chr9 | 105551256 | |||||
| chr9:105551257
|
G | A | 1 | a0001c0001t0026 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4774G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4774 | chr9 | 105551257 | |||||
| chr9:105551287
|
A | G | 1 | a0001c0001t0009 | 6 | HG00323.hp2 HG01106.hp1 HG01255.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4804A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4804 | chr9 | 105551287 | |||||
| chr9:105551355
|
C | T | 9 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(6): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4872C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4872 | chr9 | 105551355 | |||||
| chr9:105551362
|
C | T | 1 | a0001c0001t0035 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4879C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 4879 | chr9 | 105551362 | |||||
| chr9:105551485
|
T | G | 1 | a0001c0001t0016 | 3 | NA18961.hp2 NA18972.hp2 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5002T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5002 | chr9 | 105551485 | |||||
| chr9:105551871
|
A | G | 1 | a0001c0001t0031 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5388A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5388 | chr9 | 105551871 | |||||
| chr9:105551985
|
A | G | 6 | a0001c0001t0005a0001c0001t0022a0001c0001t0030others(3): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5502A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5502 | chr9 | 105551985 | |||||
| chr9:105552006
|
T | C | 6 | a0001c0001t0004a0001c0001t0010a0001c0001t0040others(3): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5523T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5523 | chr9 | 105552006 | |||||
| chr9:105552044
|
T | C | 1 | a0001c0001t0036 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5561T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5561 | chr9 | 105552044 | |||||
| chr9:105552047
|
G | C | 1 | a0003c0005t0034 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5564G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5564 | chr9 | 105552047 | |||||
| chr9:105552106
|
G | C | 1 | a0001c0001t0014 | 4 | HG02615.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5623G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5623 | chr9 | 105552106 | |||||
| chr9:105552204
|
A | AAC | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*5721_*5722insAC | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5722 | chr9 | 105552204 | |||||
| chr9:105552218
|
C | T | 8 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(5): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*5735C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5735 | chr9 | 105552218 | |||||
| chr9:105552295
|
G | GT | 6 | a0001c0001t0009a0001c0001t0010a0001c0001t0023others(3): Show | 15 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5821dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5822 | INFO_REALIGN_3_PRIME | chr9 | 105552295 | ||||
| chr9:105552319
|
G | T | 1 | a0001c0001t0027 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5836G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 14/14 | 5836 | chr9 | 105552319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:105448384
|
GCT | G | 59 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(56): Show | 60 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.15+154_15+155delCT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105448384 | |||||
| chr9:105448430
|
G | C | 88 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(85): Show | 88 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.15+195G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448430 | ||||||
| chr9:105448590
|
C | T | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+355C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448590 | ||||||
| chr9:105448624
|
T | TG | 264 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.15+389_15+390insG | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448624 | ||||||
| chr9:105448668
|
C | T | 1 | a0001c0001t0004g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.15+433C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448668 | ||||||
| chr9:105448700
|
A | C | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+465A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448700 | ||||||
| chr9:105448709
|
A | G | 163 | a0001c0001t0001g0085a0001c0001t0001g0311a0001c0001t0002g0006others(160): Show | 164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.15+474A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448709 | ||||||
| chr9:105448898
|
A | G | 38 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0153others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.15+663A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105448898 | ||||||
| chr9:105449044
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.15+809A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449044 | ||||||
| chr9:105449081
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.15+846A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449081 | ||||||
| chr9:105449152
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+917A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449152 | ||||||
| chr9:105449161
|
G | A | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+926G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449161 | ||||||
| chr9:105449533
|
C | T | 10 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0180others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.15+1298C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449533 | ||||||
| chr9:105449601
|
T | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+1366T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449601 | ||||||
| chr9:105449777
|
A | G | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15+1542A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449777 | ||||||
| chr9:105449778
|
T | TGAGGAAT others(9): Show |
276 | a0001c0001t0001g0085a0001c0001t0001g0204a0001c0001t0001g0205others(273): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.15+1546_15+1547ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105449778 | |||||
| chr9:105449778
|
T | TGAGGTAT others(9): Show |
10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+1546_15+1547ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105449778 | |||||
| chr9:105449815
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.15+1580A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449815 | ||||||
| chr9:105449862
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15+1627G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105449862 | ||||||
| chr9:105450231
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15+1996C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450231 | ||||||
| chr9:105450298
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+2063A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450298 | ||||||
| chr9:105450456
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.15+2221T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450456 | ||||||
| chr9:105450534
|
C | CT | 49 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0002g0089others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.15+2315dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105450534 | |||||
| chr9:105450534
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.15+2315_15+2316ins others(18): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105450534 | |||||
| chr9:105450534
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.15+2315_15+2316ins others(19): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105450534 | |||||
| chr9:105450723
|
G | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2488G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450723 | ||||||
| chr9:105450820
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.15+2585A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450820 | ||||||
| chr9:105450861
|
A | G | 4 | a0001c0001t0007g0199a0001c0001t0007g0200a0001c0001t0007g0201others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2626A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450861 | ||||||
| chr9:105450891
|
A | T | 1 | a0001c0001t0002g0088 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.15+2656A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105450891 | ||||||
| chr9:105451108
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+2873C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451108 | ||||||
| chr9:105451124
|
T | C | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.15+2889T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451124 | ||||||
| chr9:105451156
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.15+2921T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451156 | ||||||
| chr9:105451161
|
A | G | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+2926A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451161 | ||||||
| chr9:105451182
|
A | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+2947A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451182 | ||||||
| chr9:105451205
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15+2970C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451205 | ||||||
| chr9:105451206
|
G | A | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.15+2971G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451206 | ||||||
| chr9:105451220
|
A | G | 2 | a0001c0001t0005g0176a0001c0001t0005g0177 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.15+2985A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451220 | ||||||
| chr9:105451243
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+3008G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451243 | ||||||
| chr9:105451596
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+3361G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451596 | ||||||
| chr9:105451695
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+3460A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451695 | ||||||
| chr9:105451738
|
A | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+3503A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451738 | ||||||
| chr9:105451775
|
G | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+3540G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451775 | ||||||
| chr9:105451798
|
A | G | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG00280.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.15+3563A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451798 | ||||||
| chr9:105451912
|
A | G | 1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.15+3677A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105451912 | ||||||
| chr9:105452057
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.15+3822A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452057 | ||||||
| chr9:105452353
|
G | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+4118G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452353 | ||||||
| chr9:105452401
|
A | G | 1 | a0001c0001t0006g0374 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.15+4166A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452401 | ||||||
| chr9:105452433
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.15+4198A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452433 | ||||||
| chr9:105452460
|
G | A | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+4225G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452460 | ||||||
| chr9:105452492
|
C | T | 2 | a0001c0001t0011g0314a0001c0001t0011g0315 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.15+4257C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452492 | ||||||
| chr9:105452621
|
G | A | 1 | a0001c0001t0003g0318 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.15+4386G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452621 | ||||||
| chr9:105452625
|
G | A | 1 | a0001c0001t0002g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.15+4390G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452625 | ||||||
| chr9:105452628
|
C | CGCCT | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0229others(70): Show | 74 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.15+4434_15+4437dup others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
C | CGCCTGCC others(1): Show |
21 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0217others(18): Show | 21 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+4430_15+4437dup others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
C | CGCCTGCC others(5): Show |
5 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0005g0176others(2): Show | 5 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+4426_15+4437dup others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
C | CGCCTGCC others(5): Show |
1 | a0001c0001t0014g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.15+4403_15+4404ins others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
CGCCT | C | 9 | a0001c0001t0003g0320a0001c0001t0003g0321a0001c0001t0004g0135others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4434_15+4437del others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
CGCCTGCC others(1): Show |
C | 21 | a0001c0001t0003g0322a0001c0001t0003g0323a0001c0001t0003g0324others(18): Show | 21 | HG00558.hp2 HG00673.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+4430_15+4437del others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452628
|
CGCCTGCC others(5): Show |
C | 31 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0342others(28): Show | 32 | HG00323.hp1 HG00597.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.15+4426_15+4437del others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452628 | |||||
| chr9:105452657
|
GCCTGCCT others(9): Show |
G | 7 | a0001c0001t0003g0370a0001c0001t0003g0371a0001c0001t0003g0372others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+4426_15+4441del others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452657 | |||||
| chr9:105452661
|
G | GCCTTCCT others(9): Show |
1 | a0001c0001t0004g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.15+4429_15+4430ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452661 | |||||
| chr9:105452661
|
G | GCCTTCCT others(13): Show |
1 | a0001c0001t0004g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15+4429_15+4430ins others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452661 | |||||
| chr9:105452661
|
G | T | 6 | a0001c0001t0004g0141a0001c0001t0012g0098a0001c0001t0012g0099others(3): Show | 6 | HG00609.hp2 HG01884.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+4426G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452661 | ||||||
| chr9:105452665
|
G | GCCTT | 9 | a0001c0001t0002g0083a0001c0001t0004g0133a0001c0001t0004g0134others(6): Show | 9 | HG00323.hp2 HG01255.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4433_15+4434ins others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452665 | |||||
| chr9:105452665
|
G | GCCTTCCT others(1): Show |
10 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126others(7): Show | 10 | HG00741.hp1 HG01243.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.15+4433_15+4434ins others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452665 | |||||
| chr9:105452665
|
G | GCCTTCCT others(5): Show |
1 | a0001c0001t0004g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.15+4433_15+4434ins others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452665 | |||||
| chr9:105452665
|
G | GCCTTCCT others(9): Show |
1 | a0001c0002t0010g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+4433_15+4434ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452665 | |||||
| chr9:105452665
|
G | T | 12 | a0001c0001t0003g0320a0001c0001t0003g0321a0001c0001t0004g0138others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+4430G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452665 | ||||||
| chr9:105452665
|
GCCTGCCT others(25): Show |
G | 1 | a0001c0001t0011g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.15+4434_15+4465del others(32): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452665 | |||||
| chr9:105452669
|
G | GCCTGCCT others(17): Show |
1 | a0001c0001t0005g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.15+4437_15+4438ins others(24): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(9): Show |
1 | a0001c0001t0013g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.15+4437_15+4438ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(13): Show |
2 | a0001c0001t0005g0153a0001c0001t0030g0152 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(17): Show |
1 | a0001c0001t0005g0151 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15+4437_15+4438ins others(24): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(5): Show |
6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG01081.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(13): Show |
2 | a0001c0001t0001g0205a0001c0001t0005g0178 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(17): Show |
2 | a0001c0001t0001g0204a0001c0002t0010g0105 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(24): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(1): Show |
21 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(18): Show | 21 | HG01074.hp2 HG01109.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(5): Show |
10 | a0001c0001t0002g0015a0001c0001t0004g0106a0001c0001t0005g0156others(7): Show | 10 | HG01515.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.15+4437_15+4438ins others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(9): Show |
1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+4437_15+4438ins others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTGCCT others(13): Show |
1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.15+4437_15+4438ins others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTT | 16 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0070others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+4480_15+4483dup others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTTCCT others(1): Show |
17 | a0001c0001t0001g0212a0001c0001t0004g0001a0001c0001t0004g0117others(14): Show | 18 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.15+4476_15+4483dup others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTTCCT others(5): Show |
11 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0001t0004g0114others(8): Show | 11 | HG00099.hp1 HG00639.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+4472_15+4483dup others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTTCCT others(9): Show |
2 | a0001c0001t0004g0111a0001c0001t0005g0158 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.15+4468_15+4483dup others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | GCCTTCCT others(13): Show |
2 | a0001c0001t0004g0109a0001c0002t0010g0110 | 2 | HG01361.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.15+4464_15+4483dup others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
G | T | 55 | a0001c0001t0002g0083a0001c0001t0003g0320a0001c0001t0003g0321others(52): Show | 55 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.15+4434G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452669 | ||||||
| chr9:105452669
|
GCCTT | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0225others(24): Show | 28 | HG00673.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.15+4480_15+4483del others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
GCCTTCCT others(1): Show |
G | 4 | a0001c0001t0001g0003a0001c0001t0008g0304a0001c0001t0008g0305others(1): Show | 4 | NA18959.hp2 NA18993.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+4476_15+4483del others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452669
|
GCCTTCCT others(21): Show |
G | 3 | a0001c0001t0011g0312a0001c0001t0011g0314a0001c0001t0011g0315 | 3 | HG02723.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.15+4456_15+4483del others(28): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452669 | |||||
| chr9:105452673
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0208others(49): Show | 53 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.15+4438T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452673 | ||||||
| chr9:105452677
|
T | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0222a0001c0001t0001g0231others(21): Show | 24 | HG01109.hp2 HG02486.hp1 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.15+4442T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452677 | ||||||
| chr9:105452681
|
T | G | 5 | a0001c0001t0001g0222a0001c0001t0014g0206a0001c0001t0014g0207others(2): Show | 5 | HG01109.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+4446T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452681 | ||||||
| chr9:105452749
|
T | TTTTTC | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+4524_15+4528dup others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105452749 | |||||
| chr9:105452783
|
T | G | 1 | a0001c0001t0006g0374 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.15+4548T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452783 | ||||||
| chr9:105452953
|
C | A | 9 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(6): Show | 9 | HG02451.hp1 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4718C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452953 | ||||||
| chr9:105452980
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+4745A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105452980 | ||||||
| chr9:105453001
|
T | C | 1 | a0001c0001t0014g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+4766T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453001 | ||||||
| chr9:105453043
|
TG | T | 35 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.15+4809delG | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453043 | ||||||
| chr9:105453044
|
G | GT | 34 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0221others(31): Show | 34 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.15+4831dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105453044 | |||||
| chr9:105453044
|
G | T | 4 | a0001c0001t0005g0166a0001c0001t0005g0167a0001c0001t0005g0171others(1): Show | 4 | HG00735.hp1 HG02300.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4809G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453044 | ||||||
| chr9:105453044
|
GT | G | 22 | a0001c0001t0002g0010a0001c0001t0002g0022a0001c0001t0002g0057others(19): Show | 22 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+4831delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105453044 | |||||
| chr9:105453044
|
GTT | G | 139 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(136): Show | 140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.15+4830_15+4831del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105453044 | |||||
| chr9:105453073
|
C | T | 1 | a0001c0001t0003g0367 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.15+4838C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453073 | ||||||
| chr9:105453305
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+5070C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453305 | ||||||
| chr9:105453330
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0088a0001c0001t0002g0089 | 3 | NA18973.hp1 NA19056.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.15+5095C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453330 | ||||||
| chr9:105453493
|
T | TTG | 7 | a0001c0001t0005g0158a0001c0001t0005g0174a0001c0001t0012g0098others(4): Show | 7 | HG01884.hp1 HG02818.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+5275_15+5276dup others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105453493 | |||||
| chr9:105453510
|
T | C | 2 | a0001c0001t0024g0254a0001c0001t0024g0255 | 2 | HG00408.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.15+5275T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453510 | ||||||
| chr9:105453620
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+5385T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453620 | ||||||
| chr9:105453851
|
A | G | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.15+5616A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105453851 | ||||||
| chr9:105453870
|
A | AT | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5639dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105453870 | |||||
| chr9:105454008
|
A | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+5773A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454008 | ||||||
| chr9:105454021
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+5786C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454021 | ||||||
| chr9:105454081
|
G | A | 6 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+5846G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454081 | ||||||
| chr9:105454291
|
A | G | 1 | a0001c0001t0006g0341 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.15+6056A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454291 | ||||||
| chr9:105454340
|
G | A | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.15+6105G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454340 | ||||||
| chr9:105454356
|
T | C | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+6121T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454356 | ||||||
| chr9:105454670
|
G | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+6435G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454670 | ||||||
| chr9:105454787
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6552A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454787 | ||||||
| chr9:105454956
|
T | G | 1 | a0001c0001t0005g0181 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.16-6564T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105454956 | ||||||
| chr9:105455008
|
A | G | 1 | a0001c0001t0003g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.16-6512A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455008 | ||||||
| chr9:105455373
|
A | G | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-6147A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455373 | ||||||
| chr9:105455434
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-6086A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455434 | ||||||
| chr9:105455479
|
G | A | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-6041G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455479 | ||||||
| chr9:105455521
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.16-5999T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455521 | ||||||
| chr9:105455692
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5828A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105455692 | ||||||
| chr9:105456090
|
T | G | 1 | a0001c0001t0004g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16-5430T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456090 | ||||||
| chr9:105456135
|
C | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5385C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456135 | ||||||
| chr9:105456341
|
T | A | 5 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-5179T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456341 | ||||||
| chr9:105456504
|
T | C | 1 | a0001c0001t0002g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.16-5016T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456504 | ||||||
| chr9:105456571
|
A | G | 36 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.16-4949A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456571 | ||||||
| chr9:105456654
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-4866A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456654 | ||||||
| chr9:105456759
|
G | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG00609.hp1 NA18948.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.16-4761G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456759 | ||||||
| chr9:105456781
|
A | G | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16-4739A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456781 | ||||||
| chr9:105456810
|
A | G | 265 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(262): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.16-4710A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456810 | ||||||
| chr9:105456864
|
TATAAA | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-4652_16-4648del others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105456864 | |||||
| chr9:105456890
|
T | C | 1 | a0001c0001t0011g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.16-4630T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456890 | ||||||
| chr9:105456958
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-4562C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105456958 | ||||||
| chr9:105457024
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-4496C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457024 | ||||||
| chr9:105457185
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.16-4335T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457185 | ||||||
| chr9:105457481
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-4039C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457481 | ||||||
| chr9:105457529
|
G | A | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.16-3991G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457529 | ||||||
| chr9:105457610
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16-3910G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457610 | ||||||
| chr9:105457660
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3860C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457660 | ||||||
| chr9:105457776
|
C | A | 1 | a0001c0001t0007g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-3744C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457776 | ||||||
| chr9:105457877
|
T | C | 1 | a0001c0001t0003g0322 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.16-3643T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457877 | ||||||
| chr9:105457928
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3592G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457928 | ||||||
| chr9:105457934
|
G | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-3586G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105457934 | ||||||
| chr9:105458039
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3481C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458039 | ||||||
| chr9:105458166
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3354G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458166 | ||||||
| chr9:105458359
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3161A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458359 | ||||||
| chr9:105458423
|
G | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.16-3097G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458423 | ||||||
| chr9:105458601
|
G | A | 1 | a0001c0001t0019g0258 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.16-2919G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458601 | ||||||
| chr9:105458711
|
T | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2809T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458711 | ||||||
| chr9:105458720
|
A | G | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.16-2800A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458720 | ||||||
| chr9:105458918
|
C | T | 5 | a0001c0001t0010g0108a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG01074.hp2 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-2602C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458918 | ||||||
| chr9:105458919
|
G | A | 1 | a0001c0001t0003g0323 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.16-2601G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458919 | ||||||
| chr9:105458919
|
G | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-2601G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458919 | ||||||
| chr9:105458954
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-2566A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458954 | ||||||
| chr9:105458970
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-2550C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458970 | ||||||
| chr9:105458971
|
G | A | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.16-2549G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458971 | ||||||
| chr9:105458979
|
A | T | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.16-2541A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105458979 | ||||||
| chr9:105459007
|
C | G | 60 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(57): Show | 61 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.16-2513C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459007 | ||||||
| chr9:105459088
|
T | A | 39 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(36): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-2432T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459088 | ||||||
| chr9:105459109
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-2411G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459109 | ||||||
| chr9:105459387
|
T | C | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.16-2133T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459387 | ||||||
| chr9:105459484
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-2036C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459484 | ||||||
| chr9:105459660
|
A | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | NA18960.hp2 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-1860A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459660 | ||||||
| chr9:105459686
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.16-1834A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459686 | ||||||
| chr9:105459852
|
T | C | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-1668T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105459852 | ||||||
| chr9:105460034
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.16-1486A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460034 | ||||||
| chr9:105460358
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.16-1162G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460358 | ||||||
| chr9:105460591
|
C | CA | 70 | a0001c0001t0001g0237a0001c0001t0001g0281a0001c0001t0002g0057others(67): Show | 71 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.16-910dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105460591 | |||||
| chr9:105460591
|
CA | C | 7 | a0001c0001t0001g0225a0001c0001t0001g0273a0001c0001t0002g0014others(4): Show | 7 | HG01074.hp1 HG02257.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-910delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105460591 | |||||
| chr9:105460653
|
G | A | 1 | a0001c0001t0005g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.16-867G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460653 | ||||||
| chr9:105460657
|
G | A | 1 | a0001c0001t0009g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.16-863G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460657 | ||||||
| chr9:105460754
|
G | A | 6 | a0001c0001t0009g0188a0001c0001t0009g0190a0001c0001t0009g0191others(3): Show | 6 | HG00323.hp2 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-766G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460754 | ||||||
| chr9:105460944
|
T | C | 2 | a0001c0001t0007g0200a0001c0001t0007g0201 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.16-576T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460944 | ||||||
| chr9:105460987
|
A | G | 1 | a0001c0001t0005g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.16-533A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105460987 | ||||||
| chr9:105461047
|
CTAT | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0088a0001c0001t0002g0089 | 3 | NA18973.hp1 NA19056.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.16-469_16-467delTA others(1): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105461047 | |||||
| chr9:105461120
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-400A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105461120 | ||||||
| chr9:105461156
|
T | G | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-364T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105461156 | ||||||
| chr9:105461265
|
G | A | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-255G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105461265 | ||||||
| chr9:105461357
|
C | CA | 5 | a0001c0001t0001g0281a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-154dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr9 | 105461357 | |||||
| chr9:105461505
|
A | G | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.16-15A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 1/13 | chr9 | 105461505 | ||||||
| chr9:105461642
|
T | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+27T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461642 | ||||||
| chr9:105461745
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.111+130G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461745 | ||||||
| chr9:105461829
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.111+214C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461829 | ||||||
| chr9:105461843
|
G | A | 44 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.111+228G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461843 | ||||||
| chr9:105461860
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+245A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461860 | ||||||
| chr9:105461885
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+270T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461885 | ||||||
| chr9:105461931
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18966.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.111+316C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461931 | ||||||
| chr9:105461956
|
C | CA | 13 | a0001c0001t0001g0238a0001c0001t0002g0015a0001c0001t0002g0026others(10): Show | 13 | HG01106.hp1 HG01993.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.111+355dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105461956 | |||||
| chr9:105461956
|
CA | C | 69 | a0001c0001t0001g0212a0001c0001t0002g0019a0001c0001t0002g0020others(66): Show | 70 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.111+355delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105461956 | |||||
| chr9:105461989
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.111+374T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105461989 | ||||||
| chr9:105462101
|
G | A | 1 | a0001c0001t0009g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.111+486G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462101 | ||||||
| chr9:105462143
|
G | T | 60 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(57): Show | 61 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.111+528G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462143 | ||||||
| chr9:105462220
|
T | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+605T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462220 | ||||||
| chr9:105462518
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.111+903A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462518 | ||||||
| chr9:105462520
|
A | AT | 100 | a0001c0001t0001g0085a0001c0001t0001g0208a0001c0001t0001g0209others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.111+926dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105462520 | |||||
| chr9:105462520
|
A | ATT | 6 | a0001c0001t0001g0253a0001c0001t0002g0053a0001c0001t0002g0054others(3): Show | 6 | HG02027.hp1 HG02451.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+925_111+926dup others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105462520 | |||||
| chr9:105462520
|
A | T | 1 | a0001c0001t0002g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.111+905A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462520 | ||||||
| chr9:105462520
|
AT | A | 13 | a0001c0001t0001g0238a0001c0001t0003g0324a0001c0001t0003g0342others(10): Show | 13 | HG00558.hp2 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.111+926delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105462520 | |||||
| chr9:105462520
|
ATTT | A | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+924_111+926del others(3): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105462520 | |||||
| chr9:105462556
|
C | T | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.111+941C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462556 | ||||||
| chr9:105462635
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.111+1020G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462635 | ||||||
| chr9:105462647
|
T | C | 1 | a0001c0001t0027g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111+1032T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462647 | ||||||
| chr9:105462679
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.111+1064C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462679 | ||||||
| chr9:105462680
|
G | A | 2 | a0001c0001t0011g0312a0001c0001t0011g0313 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.111+1065G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462680 | ||||||
| chr9:105462683
|
T | C | 1 | a0001c0001t0027g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111+1068T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462683 | ||||||
| chr9:105462726
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+1111T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462726 | ||||||
| chr9:105462729
|
G | A | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+1114G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462729 | ||||||
| chr9:105462787
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.111+1172C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462787 | ||||||
| chr9:105462831
|
TTA | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(369): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.111+1220_111+1221d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105462831 | |||||
| chr9:105462879
|
T | C | 1 | a0001c0001t0042g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.111+1264T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462879 | ||||||
| chr9:105462974
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.112-1262C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462974 | ||||||
| chr9:105462988
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.112-1248A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105462988 | ||||||
| chr9:105463006
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1230C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463006 | ||||||
| chr9:105463009
|
A | G | 225 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(222): Show | 227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.112-1227A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463009 | ||||||
| chr9:105463022
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1214C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463022 | ||||||
| chr9:105463090
|
A | G | 4 | a0001c0001t0003g0005a0001c0001t0003g0361a0001c0001t0003g0362others(1): Show | 5 | HG00741.hp2 HG01099.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-1146A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463090 | ||||||
| chr9:105463138
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1098C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463138 | ||||||
| chr9:105463154
|
T | TA | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(361): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.112-1072dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr9 | 105463154 | |||||
| chr9:105463165
|
T | A | 1 | a0001c0001t0004g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.112-1071T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463165 | ||||||
| chr9:105463217
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1019G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463217 | ||||||
| chr9:105463256
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-980A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463256 | ||||||
| chr9:105463427
|
A | C | 1 | a0001c0001t0014g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112-809A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463427 | ||||||
| chr9:105463457
|
T | C | 1 | a0001c0001t0002g0011 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.112-779T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463457 | ||||||
| chr9:105463487
|
A | T | 23 | a0001c0001t0003g0324a0001c0001t0003g0336a0001c0001t0003g0337others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.112-749A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463487 | ||||||
| chr9:105463629
|
C | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.112-607C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463629 | ||||||
| chr9:105463652
|
A | G | 1 | a0001c0001t0002g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.112-584A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463652 | ||||||
| chr9:105463833
|
T | A | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0132 | 3 | HG01243.hp2 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.112-403T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105463833 | ||||||
| chr9:105464021
|
C | T | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.112-215C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 2/13 | chr9 | 105464021 | ||||||
| chr9:105464338
|
T | C | 5 | a0001c0001t0009g0188a0001c0001t0009g0191a0001c0001t0009g0193others(2): Show | 5 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.207+7T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464338 | ||||||
| chr9:105464397
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.207+66A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464397 | ||||||
| chr9:105464694
|
C | T | 1 | a0001c0001t0003g0363 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.207+363C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464694 | ||||||
| chr9:105464860
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+529A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464860 | ||||||
| chr9:105464897
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+566C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464897 | ||||||
| chr9:105464912
|
C | T | 2 | a0001c0001t0019g0258a0001c0001t0019g0294 | 2 | NA18954.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.207+581C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105464912 | ||||||
| chr9:105465032
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.207+701A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465032 | ||||||
| chr9:105465135
|
C | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+804C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465135 | ||||||
| chr9:105465193
|
A | G | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+862A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465193 | ||||||
| chr9:105465315
|
A | T | 263 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.207+984A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465315 | ||||||
| chr9:105465350
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.207+1019T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465350 | ||||||
| chr9:105465406
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.207+1075C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465406 | ||||||
| chr9:105465547
|
G | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+1216G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465547 | ||||||
| chr9:105465695
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.207+1364G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465695 | ||||||
| chr9:105465720
|
G | A | 224 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(221): Show | 226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.207+1389G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465720 | ||||||
| chr9:105465748
|
A | T | 1 | a0001c0001t0035g0232 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.207+1417A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465748 | ||||||
| chr9:105465778
|
A | T | 1 | a0001c0001t0035g0232 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.207+1447A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465778 | ||||||
| chr9:105465849
|
C | G | 1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.207+1518C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465849 | ||||||
| chr9:105465913
|
C | A | 1 | a0001c0001t0001g0239 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.207+1582C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465913 | ||||||
| chr9:105465962
|
T | C | 80 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(77): Show | 81 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.207+1631T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105465962 | ||||||
| chr9:105466001
|
ACT | A | 39 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(36): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.207+1673_207+1674d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr9 | 105466001 | |||||
| chr9:105466211
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.207+1880A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466211 | ||||||
| chr9:105466243
|
A | G | 6 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+1912A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466243 | ||||||
| chr9:105466464
|
A | G | 263 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.208-1729A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466464 | ||||||
| chr9:105466553
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.208-1640C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466553 | ||||||
| chr9:105466608
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.208-1585G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466608 | ||||||
| chr9:105466647
|
C | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0132 | 3 | HG01243.hp2 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.208-1546C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466647 | ||||||
| chr9:105466692
|
CA | C | 166 | a0001c0001t0002g0029a0001c0001t0002g0065a0001c0001t0003g0005others(163): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.208-1486delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr9 | 105466692 | |||||
| chr9:105466692
|
CAA | C | 97 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(94): Show | 97 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.208-1487_208-1486d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr9 | 105466692 | |||||
| chr9:105466700
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.208-1493A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466700 | ||||||
| chr9:105466705
|
A | T | 1 | a0001c0001t0015g0340 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.208-1488A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466705 | ||||||
| chr9:105466709
|
A | T | 1 | a0001c0001t0004g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.208-1484A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466709 | ||||||
| chr9:105466739
|
T | C | 3 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.208-1454T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105466739 | ||||||
| chr9:105467223
|
G | A | 1 | a0001c0001t0041g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208-970G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467223 | ||||||
| chr9:105467250
|
A | G | 1 | a0001c0001t0004g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.208-943A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467250 | ||||||
| chr9:105467272
|
A | G | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.208-921A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467272 | ||||||
| chr9:105467321
|
G | A | 2 | a0002c0004t0002g0016a0002c0004t0029g0074 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.208-872G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467321 | ||||||
| chr9:105467332
|
T | C | 1 | a0001c0001t0005g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208-861T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467332 | ||||||
| chr9:105467384
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-809A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467384 | ||||||
| chr9:105467709
|
A | G | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.208-484A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467709 | ||||||
| chr9:105467731
|
C | T | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.208-462C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467731 | ||||||
| chr9:105467796
|
A | G | 7 | a0001c0001t0001g0300a0001c0001t0008g0296a0001c0001t0008g0297others(4): Show | 7 | NA18940.hp2 NA18949.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-397A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467796 | ||||||
| chr9:105467895
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.208-298C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105467895 | ||||||
| chr9:105468012
|
G | A | 6 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-181G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105468012 | ||||||
| chr9:105468143
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.208-50A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 3/13 | chr9 | 105468143 | ||||||
| chr9:105468385
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+61A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468385 | ||||||
| chr9:105468392
|
A | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0051others(3): Show | 6 | HG02148.hp1 HG02273.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+68A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468392 | ||||||
| chr9:105468428
|
C | T | 61 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.339+104C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468428 | ||||||
| chr9:105468507
|
A | AT | 6 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0281others(3): Show | 6 | HG00735.hp2 NA18948.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+198dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105468507 | |||||
| chr9:105468507
|
AT | A | 7 | a0001c0001t0002g0014a0001c0001t0002g0067a0001c0001t0013g0094others(4): Show | 7 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+198delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105468507 | |||||
| chr9:105468527
|
C | T | 1 | a0001c0001t0014g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.339+203C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468527 | ||||||
| chr9:105468595
|
G | A | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.339+271G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468595 | ||||||
| chr9:105468597
|
C | T | 1 | a0001c0001t0003g0364 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.339+273C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468597 | ||||||
| chr9:105468685
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.339+361G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468685 | ||||||
| chr9:105468735
|
TC | T | 7 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+413delC | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105468735 | |||||
| chr9:105468917
|
G | C | 1 | a0001c0001t0002g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.339+593G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105468917 | ||||||
| chr9:105469036
|
C | T | 264 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.339+712C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469036 | ||||||
| chr9:105469092
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.339+768A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469092 | ||||||
| chr9:105469110
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+786G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469110 | ||||||
| chr9:105469136
|
A | G | 6 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+812A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469136 | ||||||
| chr9:105469171
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+847C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469171 | ||||||
| chr9:105469220
|
A | G | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+896A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469220 | ||||||
| chr9:105469335
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339+1011G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469335 | ||||||
| chr9:105469378
|
A | AT | 264 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.339+1055dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105469378 | |||||
| chr9:105469401
|
A | G | 1 | a0001c0001t0004g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339+1077A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469401 | ||||||
| chr9:105469438
|
G | GT | 61 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.339+1124dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105469438 | |||||
| chr9:105469542
|
G | A | 1 | a0001c0001t0007g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.339+1218G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469542 | ||||||
| chr9:105469655
|
T | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+1331T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469655 | ||||||
| chr9:105469665
|
C | T | 2 | a0002c0004t0002g0016a0002c0004t0029g0074 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.339+1341C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469665 | ||||||
| chr9:105469673
|
T | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1349T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469673 | ||||||
| chr9:105469702
|
GT | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(255): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.339+1393delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105469702 | |||||
| chr9:105469702
|
GTT | G | 73 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215others(70): Show | 74 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.339+1392_339+1393d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105469702 | |||||
| chr9:105469717
|
T | C | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.339+1393T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469717 | ||||||
| chr9:105469819
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1495G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469819 | ||||||
| chr9:105469822
|
A | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1498A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469822 | ||||||
| chr9:105469985
|
C | T | 1 | a0001c0001t0024g0255 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.339+1661C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105469985 | ||||||
| chr9:105470024
|
C | T | 1 | a0001c0001t0005g0157 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.339+1700C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470024 | ||||||
| chr9:105470040
|
T | C | 6 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+1716T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470040 | ||||||
| chr9:105470048
|
A | G | 1 | a0001c0001t0003g0366 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.339+1724A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470048 | ||||||
| chr9:105470049
|
T | A | 5 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+1725T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470049 | ||||||
| chr9:105470109
|
A | G | 102 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(99): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.339+1785A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470109 | ||||||
| chr9:105470159
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.340-1745A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470159 | ||||||
| chr9:105470265
|
A | G | 6 | a0001c0001t0003g0005a0001c0001t0003g0350a0001c0001t0003g0361others(3): Show | 7 | HG00741.hp2 HG01099.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1639A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470265 | ||||||
| chr9:105470268
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-1636T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470268 | ||||||
| chr9:105470498
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.340-1406C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470498 | ||||||
| chr9:105470653
|
A | G | 1 | a0001c0001t0011g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.340-1251A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470653 | ||||||
| chr9:105470657
|
T | C | 3 | a0001c0001t0022g0170a0001c0001t0022g0173a0001c0001t0032g0163 | 3 | HG02615.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.340-1247T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470657 | ||||||
| chr9:105470756
|
G | A | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.340-1148G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470756 | ||||||
| chr9:105470831
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.340-1073C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470831 | ||||||
| chr9:105470894
|
C | T | 75 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(72): Show | 76 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.340-1010C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470894 | ||||||
| chr9:105470933
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-971T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105470933 | ||||||
| chr9:105471350
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-554G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471350 | ||||||
| chr9:105471459
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.340-445C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471459 | ||||||
| chr9:105471516
|
A | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-388A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471516 | ||||||
| chr9:105471610
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.340-294T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471610 | ||||||
| chr9:105471706
|
TA | T | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-190delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471706 | |||||
| chr9:105471708
|
A | T | 1 | a0001c0001t0003g0360 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.340-196A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471708 | ||||||
| chr9:105471713
|
AAT | A | 6 | a0001c0001t0002g0092a0001c0001t0012g0101a0001c0001t0013g0094others(3): Show | 6 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-189_340-188del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471713 | |||||
| chr9:105471714
|
AT | A | 7 | a0001c0001t0002g0015a0001c0001t0003g0351a0001c0001t0003g0352others(4): Show | 7 | HG01884.hp1 HG02818.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-189delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471714 | ||||||
| chr9:105471724
|
T | TTA | 24 | a0001c0001t0001g0085a0001c0001t0001g0216a0001c0001t0001g0238others(21): Show | 24 | HG01515.hp2 HG02165.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.340-159_340-158dup others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
T | TTATA | 70 | a0001c0001t0001g0222a0001c0001t0002g0006a0001c0001t0002g0009others(67): Show | 71 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.340-161_340-158dup others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
T | TTATATA | 56 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0017others(53): Show | 56 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.340-163_340-158dup others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
T | TTATATAT others(1): Show |
5 | a0001c0001t0002g0027a0001c0001t0007g0199a0001c0001t0009g0191others(2): Show | 5 | HG00323.hp2 HG01884.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-165_340-158dup others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
T | TTATATAT others(3): Show |
3 | a0001c0001t0012g0099a0001c0001t0012g0100a0001c0001t0012g0101 | 3 | HG02818.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.340-167_340-158dup others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
TTA | T | 28 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0005g0146others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.340-159_340-158del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
TTATA | T | 10 | a0001c0001t0005g0178a0001c0001t0005g0179a0001c0001t0005g0180others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-161_340-158del others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471724
|
TTATATA | T | 6 | a0001c0001t0003g0350a0001c0001t0011g0312a0001c0001t0011g0313others(3): Show | 6 | HG02723.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-163_340-158del others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471724 | |||||
| chr9:105471726
|
A | T | 3 | a0001c0001t0013g0095a0001c0001t0013g0096a0001c0001t0036g0359 | 3 | HG01255.hp2 HG03098.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.340-178A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471726 | ||||||
| chr9:105471732
|
A | T | 1 | a0001c0001t0013g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340-172A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471732 | ||||||
| chr9:105471745
|
T | A | 1 | a0001c0001t0006g0341 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.340-159T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | chr9 | 105471745 | ||||||
| chr9:105471882
|
G | GT | 109 | a0001c0001t0001g0085a0001c0001t0001g0290a0001c0001t0002g0006others(106): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.340-7dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr9 | 105471882 | |||||
| chr9:105472013
|
A | G | 4 | a0001c0001t0001g0230a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG01433.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.441+8A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472013 | ||||||
| chr9:105472094
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+89A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472094 | ||||||
| chr9:105472320
|
CA | C | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0038others(3): Show | 6 | NA18963.hp2 NA18991.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+316delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472320 | ||||||
| chr9:105472612
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+607G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472612 | ||||||
| chr9:105472662
|
G | T | 1 | a0001c0001t0026g0012 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.441+657G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472662 | ||||||
| chr9:105472718
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.441+713G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472718 | ||||||
| chr9:105472854
|
TGAATC | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+850_441+854del others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472854 | ||||||
| chr9:105472963
|
A | G | 1 | a0001c0001t0007g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.441+958A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105472963 | ||||||
| chr9:105473162
|
C | T | 4 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0174others(1): Show | 4 | HG00280.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1157C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473162 | ||||||
| chr9:105473211
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1206T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473211 | ||||||
| chr9:105473330
|
C | G | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.441+1325C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473330 | ||||||
| chr9:105473473
|
A | C | 1 | a0001c0002t0010g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+1468A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473473 | ||||||
| chr9:105473635
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.441+1630C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473635 | ||||||
| chr9:105473677
|
C | T | 1 | a0001c0001t0043g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.441+1672C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473677 | ||||||
| chr9:105473789
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1784A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473789 | ||||||
| chr9:105473940
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1935C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473940 | ||||||
| chr9:105473967
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+1962T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105473967 | ||||||
| chr9:105474049
|
G | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+2044G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474049 | ||||||
| chr9:105474081
|
A | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+2076A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474081 | ||||||
| chr9:105474118
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2113A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474118 | ||||||
| chr9:105474344
|
G | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+2339G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474344 | ||||||
| chr9:105474437
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.441+2432G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474437 | ||||||
| chr9:105474465
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.441+2460G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474465 | ||||||
| chr9:105474523
|
A | G | 62 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.441+2518A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474523 | ||||||
| chr9:105474639
|
T | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.441+2634T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474639 | ||||||
| chr9:105474724
|
A | G | 2 | a0001c0001t0005g0176a0001c0001t0005g0177 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.441+2719A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474724 | ||||||
| chr9:105474779
|
A | G | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+2774A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474779 | ||||||
| chr9:105474820
|
C | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0308 | 2 | HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.441+2815C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474820 | ||||||
| chr9:105474961
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2956G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105474961 | ||||||
| chr9:105475183
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.441+3178A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475183 | ||||||
| chr9:105475321
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441+3316A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475321 | ||||||
| chr9:105475404
|
C | T | 1 | a0001c0001t0015g0340 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.441+3399C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475404 | ||||||
| chr9:105475501
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.441+3496A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475501 | ||||||
| chr9:105475643
|
C | T | 225 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(222): Show | 227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.441+3638C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475643 | ||||||
| chr9:105475713
|
A | G | 263 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.442-3641A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475713 | ||||||
| chr9:105475746
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0020others(14): Show | 17 | HG00642.hp1 HG01358.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-3608C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475746 | ||||||
| chr9:105475823
|
C | A | 1 | a0001c0001t0011g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.442-3531C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475823 | ||||||
| chr9:105475944
|
A | G | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-3410A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475944 | ||||||
| chr9:105475955
|
G | T | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3399G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475955 | ||||||
| chr9:105475957
|
C | T | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3397C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105475957 | ||||||
| chr9:105476013
|
A | G | 263 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.442-3341A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476013 | ||||||
| chr9:105476065
|
A | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0132 | 3 | HG01243.hp2 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.442-3289A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476065 | ||||||
| chr9:105476092
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-3262A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476092 | ||||||
| chr9:105476142
|
C | G | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.442-3212C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476142 | ||||||
| chr9:105476161
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-3193T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476161 | ||||||
| chr9:105476366
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.442-2988A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476366 | ||||||
| chr9:105476892
|
C | T | 2 | a0001c0001t0005g0167a0001c0001t0005g0169 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.442-2462C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105476892 | ||||||
| chr9:105477299
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-2055A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105477299 | ||||||
| chr9:105477395
|
A | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.442-1959A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105477395 | ||||||
| chr9:105477525
|
A | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.442-1829A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105477525 | ||||||
| chr9:105477652
|
TTTCC | T | 10 | a0001c0001t0002g0008a0001c0001t0002g0021a0001c0001t0002g0031others(7): Show | 10 | HG02056.hp2 HG02165.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-1695_442-1692d others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr9 | 105477652 | |||||
| chr9:105477980
|
C | T | 39 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(36): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.442-1374C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105477980 | ||||||
| chr9:105478177
|
A | G | 8 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(5): Show | 8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1177A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478177 | ||||||
| chr9:105478288
|
C | A | 8 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(5): Show | 8 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-1066C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478288 | ||||||
| chr9:105478516
|
G | A | 255 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(252): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.442-838G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478516 | ||||||
| chr9:105478540
|
A | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.442-814A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478540 | ||||||
| chr9:105478813
|
A | G | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.442-541A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478813 | ||||||
| chr9:105478855
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-499C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478855 | ||||||
| chr9:105478885
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-469G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478885 | ||||||
| chr9:105478933
|
C | A | 3 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.442-421C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478933 | ||||||
| chr9:105478971
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-383A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 5/13 | chr9 | 105478971 | ||||||
| chr9:105479818
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.464+442A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105479818 | ||||||
| chr9:105480010
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+634T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480010 | ||||||
| chr9:105480294
|
C | CT | 106 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(103): Show | 106 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.464+934dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105480294 | |||||
| chr9:105480294
|
C | CTT | 13 | a0001c0001t0002g0076a0001c0001t0012g0098a0001c0001t0012g0099others(10): Show | 13 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.464+933_464+934dup others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105480294 | |||||
| chr9:105480356
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0302 | 2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.464+980G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480356 | ||||||
| chr9:105480443
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.464+1067C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480443 | ||||||
| chr9:105480516
|
G | T | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+1140G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480516 | ||||||
| chr9:105480558
|
C | G | 39 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(36): Show | 40 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.464+1182C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480558 | ||||||
| chr9:105480560
|
G | A | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.464+1184G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480560 | ||||||
| chr9:105480608
|
A | AT | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+1238dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105480608 | |||||
| chr9:105480644
|
A | G | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.464+1268A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480644 | ||||||
| chr9:105480799
|
T | C | 1 | a0001c0001t0042g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.464+1423T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480799 | ||||||
| chr9:105480965
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0237 | 3 | HG01346.hp1 HG02004.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.464+1589G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480965 | ||||||
| chr9:105480973
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+1597A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105480973 | ||||||
| chr9:105481023
|
C | A | 4 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0153others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+1647C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481023 | ||||||
| chr9:105481141
|
C | CTG | 16 | a0001c0001t0001g0228a0001c0001t0001g0250a0001c0001t0001g0261others(13): Show | 16 | HG00438.hp2 HG00673.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.464+1802_464+1803d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTG | 6 | a0001c0001t0001g0003a0001c0001t0001g0213a0001c0001t0001g0298others(3): Show | 7 | HG01106.hp2 HG01168.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+1800_464+1803d others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTG | 18 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0214others(15): Show | 18 | HG01069.hp1 HG01081.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.464+1798_464+1803d others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG00280.hp1 HG01243.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.464+1796_464+1803d others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(3): Show |
9 | a0001c0001t0002g0054a0001c0001t0005g0151a0001c0001t0005g0153others(6): Show | 9 | HG01109.hp1 HG02027.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.464+1794_464+1803d others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(5): Show |
18 | a0001c0001t0002g0007a0001c0001t0002g0029a0001c0001t0002g0033others(15): Show | 18 | HG00140.hp2 HG02155.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.464+1792_464+1803d others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(7): Show |
27 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0021others(24): Show | 27 | HG01099.hp1 HG01167.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.464+1790_464+1803d others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(9): Show |
27 | a0001c0001t0002g0009a0001c0001t0002g0014a0001c0001t0002g0019others(24): Show | 27 | HG00558.hp1 HG00621.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.464+1788_464+1803d others(18): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(11): Show |
19 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0020others(16): Show | 19 | HG00408.hp2 HG00609.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.464+1786_464+1803d others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(13): Show |
9 | a0001c0001t0002g0010a0001c0001t0002g0018a0001c0001t0002g0022others(6): Show | 9 | HG00642.hp1 HG01255.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.464+1784_464+1803d others(22): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(15): Show |
2 | a0001c0001t0002g0036a0001c0001t0009g0197 | 2 | HG00323.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.464+1782_464+1803d others(24): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(17): Show |
2 | a0001c0001t0002g0015a0001c0001t0002g0065 | 2 | NA18967.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.464+1780_464+1803d others(26): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(19): Show |
1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.464+1778_464+1803d others(28): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(21): Show |
1 | a0001c0001t0009g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.464+1776_464+1803d others(30): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
C | CTGTGTGT others(22): Show |
1 | a0001c0001t0002g0024 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.464+1788_464+1789i others(31): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
CTG | C | 34 | a0001c0001t0002g0052a0001c0001t0002g0055a0001c0001t0002g0073others(31): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.464+1802_464+1803d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
CTGTG | C | 7 | a0001c0001t0005g0164a0001c0001t0005g0167a0001c0001t0005g0169others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+1800_464+1803d others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0004g0203a0001c0001t0033g0155a0001c0001t0042g0147 | 3 | NA19043.hp1 NA20905.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.464+1796_464+1803d others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
CTGTGTGT others(3): Show |
C | 7 | a0001c0001t0001g0216a0001c0001t0005g0158a0001c0001t0005g0172others(4): Show | 7 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.464+1794_464+1803d others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481141
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0001t0001g0262a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.464+1792_464+1803d others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481141 | |||||
| chr9:105481156
|
T | C | 1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.464+1780T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481156 | ||||||
| chr9:105481176
|
T | TGTGTGTG others(3): Show |
45 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(42): Show | 46 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.464+1803_464+1804i others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481176 | |||||
| chr9:105481176
|
T | TGTGTGTG others(5): Show |
15 | a0001c0001t0003g0236a0001c0001t0003g0323a0001c0001t0003g0349others(12): Show | 15 | HG01167.hp2 HG01261.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.464+1803_464+1804i others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481176 | |||||
| chr9:105481176
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0003g0370a0001c0001t0003g0371 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.464+1803_464+1804i others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481176 | |||||
| chr9:105481179
|
G | GTGTGTGT others(6): Show |
1 | a0001c0001t0002g0013 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.464+1803_464+1804i others(15): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481179 | ||||||
| chr9:105481183
|
C | CT | 18 | a0001c0001t0001g0251a0001c0001t0001g0277a0001c0001t0001g0287others(15): Show | 18 | HG00438.hp1 HG01109.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.464+1828dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481183 | |||||
| chr9:105481183
|
CT | C | 8 | a0001c0001t0001g0215a0001c0001t0003g0354a0001c0001t0004g0130others(5): Show | 8 | HG01081.hp2 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.464+1828delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481183 | |||||
| chr9:105481204
|
T | G | 1 | a0001c0001t0005g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.464+1828T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481204 | ||||||
| chr9:105481212
|
C | T | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.464+1836C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481212 | ||||||
| chr9:105481220
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.464+1844A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481220 | ||||||
| chr9:105481351
|
C | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.464+1975C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481351 | ||||||
| chr9:105481431
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.464+2055C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481431 | ||||||
| chr9:105481444
|
C | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.464+2068C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481444 | ||||||
| chr9:105481457
|
G | T | 1 | a0001c0001t0012g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.464+2081G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481457 | ||||||
| chr9:105481505
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.464+2129C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481505 | ||||||
| chr9:105481618
|
T | A | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.464+2242T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481618 | ||||||
| chr9:105481774
|
G | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.464+2398G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481774 | ||||||
| chr9:105481776
|
A | AT | 10 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0286others(7): Show | 10 | HG02027.hp1 HG02155.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.464+2414dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr9 | 105481776 | |||||
| chr9:105481916
|
G | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.465-2465G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105481916 | ||||||
| chr9:105482073
|
C | A | 3 | a0001c0001t0022g0170a0001c0001t0022g0173a0001c0001t0032g0163 | 3 | HG02615.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.465-2308C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482073 | ||||||
| chr9:105482107
|
T | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.465-2274T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482107 | ||||||
| chr9:105482111
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.465-2270A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482111 | ||||||
| chr9:105482123
|
G | A | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0057 | 3 | NA18953.hp2 NA18979.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.465-2258G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482123 | ||||||
| chr9:105482151
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.465-2230T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482151 | ||||||
| chr9:105482196
|
A | G | 1 | a0001c0001t0037g0154 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.465-2185A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482196 | ||||||
| chr9:105482295
|
A | G | 75 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(72): Show | 76 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.465-2086A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482295 | ||||||
| chr9:105482323
|
G | A | 1 | a0001c0001t0004g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.465-2058G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482323 | ||||||
| chr9:105482511
|
T | C | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465-1870T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482511 | ||||||
| chr9:105482609
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.465-1772C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482609 | ||||||
| chr9:105482699
|
T | G | 62 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.465-1682T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482699 | ||||||
| chr9:105482799
|
G | A | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.465-1582G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482799 | ||||||
| chr9:105482852
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0044 | 2 | NA18990.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.465-1529C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482852 | ||||||
| chr9:105482898
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.465-1483T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105482898 | ||||||
| chr9:105483083
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.465-1298C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483083 | ||||||
| chr9:105483368
|
C | A | 1 | a0001c0001t0003g0375 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.465-1013C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483368 | ||||||
| chr9:105483412
|
T | C | 1 | a0002c0004t0029g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.465-969T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483412 | ||||||
| chr9:105483445
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-936A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483445 | ||||||
| chr9:105483515
|
G | C | 1 | a0001c0001t0015g0340 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.465-866G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483515 | ||||||
| chr9:105483760
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.465-621C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483760 | ||||||
| chr9:105483768
|
T | G | 1 | a0001c0001t0002g0057 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.465-613T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483768 | ||||||
| chr9:105483803
|
C | G | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.465-578C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105483803 | ||||||
| chr9:105484061
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.465-320C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484061 | ||||||
| chr9:105484092
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.465-289G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484092 | ||||||
| chr9:105484187
|
C | T | 1 | a0001c0001t0007g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.465-194C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484187 | ||||||
| chr9:105484329
|
T | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.465-52T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484329 | ||||||
| chr9:105484364
|
G | A | 1 | a0001c0001t0004g0001 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.465-17G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484364 | ||||||
| chr9:105484377
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.465-4G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 6/13 | chr9 | 105484377 | ||||||
| chr9:105484535
|
T | TA | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.586+37dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105484535 | |||||
| chr9:105484600
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+98A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105484600 | ||||||
| chr9:105484772
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+270T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105484772 | ||||||
| chr9:105485064
|
G | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.586+562G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485064 | ||||||
| chr9:105485328
|
A | G | 1 | a0001c0001t0005g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.586+826A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485328 | ||||||
| chr9:105485332
|
CAA | C | 3 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.586+831_586+832del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485332 | ||||||
| chr9:105485345
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+843C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485345 | ||||||
| chr9:105485356
|
A | G | 1 | a0001c0001t0006g0374 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.586+854A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485356 | ||||||
| chr9:105485532
|
T | TG | 52 | a0001c0001t0003g0005a0001c0001t0003g0318a0001c0001t0003g0320others(49): Show | 53 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.586+1031dupG | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485532 | |||||
| chr9:105485533
|
G | GGT | 9 | a0001c0001t0003g0236a0001c0001t0003g0335a0001c0001t0003g0338others(6): Show | 9 | HG01258.hp2 HG01934.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+1031_586+1032i others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485533 | ||||||
| chr9:105485533
|
G | GT | 47 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0205others(44): Show | 49 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.586+1054dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485533 | |||||
| chr9:105485533
|
G | GTT | 83 | a0001c0001t0001g0085a0001c0001t0001g0249a0001c0001t0001g0287others(80): Show | 84 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.586+1053_586+1054d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485533 | |||||
| chr9:105485533
|
G | GTTT | 28 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.586+1052_586+1054d others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485533 | |||||
| chr9:105485533
|
GT | G | 54 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0143others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.586+1054delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485533 | |||||
| chr9:105485534
|
T | G | 1 | a0001c0001t0003g0358 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.586+1032T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485534 | ||||||
| chr9:105485545
|
T | G | 1 | a0001c0001t0001g0295 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.586+1043T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485545 | ||||||
| chr9:105485670
|
G | A | 37 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.586+1168G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485670 | ||||||
| chr9:105485703
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586+1201G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485703 | ||||||
| chr9:105485705
|
A | G | 18 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(15): Show | 18 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.586+1203A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485705 | ||||||
| chr9:105485706
|
C | T | 1 | a0001c0001t0004g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.586+1204C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485706 | ||||||
| chr9:105485712
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+1210C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485712 | ||||||
| chr9:105485713
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+1211G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485713 | ||||||
| chr9:105485742
|
T | C | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.586+1240T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485742 | ||||||
| chr9:105485753
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.586+1251C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485753 | ||||||
| chr9:105485765
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+1263T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485765 | ||||||
| chr9:105485780
|
A | T | 1 | a0001c0001t0004g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.586+1278A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485780 | ||||||
| chr9:105485804
|
T | C | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.586+1302T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485804 | ||||||
| chr9:105485870
|
C | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0132 | 3 | HG01243.hp2 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.586+1368C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485870 | ||||||
| chr9:105485895
|
G | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+1393G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105485895 | ||||||
| chr9:105485999
|
CCTTGAAT others(54): Show |
C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+1500_586+1560d others(63): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105485999 | |||||
| chr9:105486007
|
A | C | 2 | a0001c0001t0003g0370a0001c0001t0003g0371 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.586+1505A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486007 | ||||||
| chr9:105486152
|
A | G | 3 | a0001c0001t0003g0351a0001c0001t0003g0352a0001c0001t0003g0353 | 3 | NA18951.hp2 NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.586+1650A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486152 | ||||||
| chr9:105486260
|
A | G | 14 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.586+1758A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486260 | ||||||
| chr9:105486431
|
G | T | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.586+1929G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486431 | ||||||
| chr9:105486455
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.586+1953T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486455 | ||||||
| chr9:105486470
|
T | A | 1 | a0001c0001t0024g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.586+1968T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486470 | ||||||
| chr9:105486562
|
T | C | 1 | a0001c0001t0003g0363 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.586+2060T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486562 | ||||||
| chr9:105486782
|
G | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0044 | 3 | HG02083.hp2 NA18990.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.586+2280G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486782 | ||||||
| chr9:105486845
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+2343C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486845 | ||||||
| chr9:105486952
|
A | T | 2 | a0001c0001t0013g0095a0001c0001t0013g0096 | 2 | HG01255.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.586+2450A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486952 | ||||||
| chr9:105486976
|
C | T | 1 | a0001c0001t0003g0320 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.586+2474C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486976 | ||||||
| chr9:105486977
|
G | T | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586+2475G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105486977 | ||||||
| chr9:105487199
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+2697A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487199 | ||||||
| chr9:105487213
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.586+2711T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487213 | ||||||
| chr9:105487424
|
G | GT | 7 | a0001c0001t0001g0308a0001c0001t0002g0057a0001c0001t0002g0090others(4): Show | 7 | HG01168.hp1 HG02071.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+2934dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105487424 | |||||
| chr9:105487424
|
GT | G | 6 | a0001c0001t0002g0014a0001c0001t0003g0005a0001c0001t0003g0350others(3): Show | 7 | HG00741.hp2 HG01099.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+2934delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105487424 | |||||
| chr9:105487607
|
G | T | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3105G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487607 | ||||||
| chr9:105487608
|
T | A | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3106T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487608 | ||||||
| chr9:105487612
|
G | T | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3110G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487612 | ||||||
| chr9:105487613
|
T | A | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3111T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487613 | ||||||
| chr9:105487613
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+3111T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487613 | ||||||
| chr9:105487615
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3113G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487615 | ||||||
| chr9:105487616
|
G | T | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3114G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487616 | ||||||
| chr9:105487618
|
C | T | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3116C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487618 | ||||||
| chr9:105487620
|
T | A | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+3118T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487620 | ||||||
| chr9:105487714
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+3212T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487714 | ||||||
| chr9:105487846
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+3344C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487846 | ||||||
| chr9:105487897
|
A | T | 54 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(51): Show | 55 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+3395A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487897 | ||||||
| chr9:105487979
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3477C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487979 | ||||||
| chr9:105487991
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+3489A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105487991 | ||||||
| chr9:105488111
|
A | G | 1 | a0001c0001t0003g0337 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.586+3609A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488111 | ||||||
| chr9:105488136
|
C | T | 1 | a0001c0001t0007g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.586+3634C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488136 | ||||||
| chr9:105488290
|
T | C | 1 | a0001c0001t0005g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.586+3788T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488290 | ||||||
| chr9:105488368
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3866T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488368 | ||||||
| chr9:105488408
|
G | GTTTA | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+3909_586+3912d others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105488408 | |||||
| chr9:105488510
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+4008A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488510 | ||||||
| chr9:105488555
|
T | C | 54 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(51): Show | 55 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+4053T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488555 | ||||||
| chr9:105488578
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.586+4076T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488578 | ||||||
| chr9:105488722
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+4220G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488722 | ||||||
| chr9:105488819
|
G | GT | 54 | a0001c0001t0001g0250a0001c0001t0001g0265a0001c0001t0001g0277others(51): Show | 55 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+4333dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105488819 | |||||
| chr9:105488819
|
GT | G | 41 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.586+4333delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105488819 | |||||
| chr9:105488842
|
A | G | 1 | a0001c0001t0004g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.586+4340A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488842 | ||||||
| chr9:105488891
|
A | G | 1 | a0001c0001t0009g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.586+4389A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488891 | ||||||
| chr9:105488909
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586+4407A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488909 | ||||||
| chr9:105488911
|
C | G | 1 | a0001c0001t0001g0002 | 2 | NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.586+4409C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488911 | ||||||
| chr9:105488973
|
T | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+4471T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105488973 | ||||||
| chr9:105489046
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.586+4544G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489046 | ||||||
| chr9:105489119
|
A | C | 47 | a0001c0001t0003g0322a0001c0001t0003g0323a0001c0001t0003g0325others(44): Show | 48 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.586+4617A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489119 | ||||||
| chr9:105489205
|
C | T | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+4703C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489205 | ||||||
| chr9:105489209
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.586+4707C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489209 | ||||||
| chr9:105489241
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.586+4739A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489241 | ||||||
| chr9:105489501
|
T | TTTTTA | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+5007_586+5011d others(7): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105489501 | |||||
| chr9:105489536
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.586+5034G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489536 | ||||||
| chr9:105489604
|
A | G | 1 | a0001c0001t0003g0342 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.586+5102A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489604 | ||||||
| chr9:105489631
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0280 | 2 | HG00621.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.586+5129A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489631 | ||||||
| chr9:105489700
|
A | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+5198A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489700 | ||||||
| chr9:105489759
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+5257G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489759 | ||||||
| chr9:105489777
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+5275T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489777 | ||||||
| chr9:105489837
|
A | T | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.586+5335A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489837 | ||||||
| chr9:105489916
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+5414T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105489916 | ||||||
| chr9:105490094
|
G | A | 3 | a0001c0001t0002g0073a0001c0001t0002g0077a0001c0001t0002g0081 | 3 | NA19001.hp2 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.586+5592G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490094 | ||||||
| chr9:105490133
|
C | T | 2 | a0001c0001t0004g0123a0001c0001t0005g0186 | 2 | HG01257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.586+5631C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490133 | ||||||
| chr9:105490134
|
G | A | 54 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(51): Show | 55 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+5632G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490134 | ||||||
| chr9:105490138
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+5636C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490138 | ||||||
| chr9:105490155
|
C | T | 279 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(276): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.586+5653C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490155 | ||||||
| chr9:105490251
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+5749G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490251 | ||||||
| chr9:105490332
|
G | A | 54 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(51): Show | 55 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+5830G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490332 | ||||||
| chr9:105490348
|
A | G | 278 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0209others(275): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.586+5846A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490348 | ||||||
| chr9:105490351
|
T | G | 1 | a0001c0001t0009g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.586+5849T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490351 | ||||||
| chr9:105490353
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.586+5851T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490353 | ||||||
| chr9:105490439
|
C | T | 1 | a0001c0001t0014g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.586+5937C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490439 | ||||||
| chr9:105490504
|
G | T | 1 | a0001c0001t0004g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.586+6002G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490504 | ||||||
| chr9:105490512
|
A | G | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6010A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490512 | ||||||
| chr9:105490520
|
G | T | 5 | a0001c0001t0033g0155a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+6018G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490520 | ||||||
| chr9:105490533
|
G | A | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+6031G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490533 | ||||||
| chr9:105490533
|
G | T | 1 | a0001c0001t0004g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.586+6031G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490533 | ||||||
| chr9:105490642
|
T | A | 5 | a0001c0001t0001g0240a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | NA18970.hp2 NA18977.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+6140T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490642 | ||||||
| chr9:105490673
|
G | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+6171G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490673 | ||||||
| chr9:105490703
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6201C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490703 | ||||||
| chr9:105490729
|
G | C | 221 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(218): Show | 223 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.586+6227G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490729 | ||||||
| chr9:105490771
|
C | T | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.586+6269C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490771 | ||||||
| chr9:105490777
|
T | G | 374 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.586+6275T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490777 | ||||||
| chr9:105490781
|
G | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6279G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490781 | ||||||
| chr9:105490787
|
C | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6285C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490787 | ||||||
| chr9:105490801
|
A | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6299A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490801 | ||||||
| chr9:105490820
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6318A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490820 | ||||||
| chr9:105490823
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6321C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490823 | ||||||
| chr9:105490824
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6322A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490824 | ||||||
| chr9:105490826
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6324C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490826 | ||||||
| chr9:105490827
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6325G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490827 | ||||||
| chr9:105490832
|
T | A | 1 | a0001c0001t0003g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.586+6330T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490832 | ||||||
| chr9:105490845
|
G | C | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.586+6343G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490845 | ||||||
| chr9:105490859
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6357A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490859 | ||||||
| chr9:105490918
|
A | G | 1 | a0001c0001t0040g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586+6416A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490918 | ||||||
| chr9:105490986
|
T | C | 4 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0153others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6484T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490986 | ||||||
| chr9:105490997
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.586+6495T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105490997 | ||||||
| chr9:105491049
|
A | G | 8 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0217others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+6547A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491049 | ||||||
| chr9:105491180
|
A | C | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+6678A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491180 | ||||||
| chr9:105491241
|
T | C | 226 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(223): Show | 228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.586+6739T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491241 | ||||||
| chr9:105491268
|
A | G | 5 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+6766A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491268 | ||||||
| chr9:105491296
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6794G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491296 | ||||||
| chr9:105491300
|
C | CTCTGTTT others(1): Show |
14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+6804_586+6805i others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105491300 | |||||
| chr9:105491371
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6869G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491371 | ||||||
| chr9:105491436
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6934G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491436 | ||||||
| chr9:105491556
|
A | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+7054A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491556 | ||||||
| chr9:105491559
|
G | A | 5 | a0001c0001t0001g0241a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+7057G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491559 | ||||||
| chr9:105491643
|
G | A | 1 | a0001c0001t0004g0115 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.586+7141G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491643 | ||||||
| chr9:105491814
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+7312T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491814 | ||||||
| chr9:105491983
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.586+7481G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491983 | ||||||
| chr9:105491989
|
G | C | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.586+7487G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491989 | ||||||
| chr9:105491990
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.586+7488G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491990 | ||||||
| chr9:105491991
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+7489T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491991 | ||||||
| chr9:105491992
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+7490A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491992 | ||||||
| chr9:105491995
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7493A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105491995 | ||||||
| chr9:105492012
|
G | A | 262 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(259): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.586+7510G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492012 | ||||||
| chr9:105492043
|
T | TC | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7541_586+7542i others(3): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492043 | ||||||
| chr9:105492089
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7587G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492089 | ||||||
| chr9:105492145
|
G | C | 1 | a0001c0001t0004g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.586+7643G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492145 | ||||||
| chr9:105492155
|
G | A | 54 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(51): Show | 55 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+7653G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492155 | ||||||
| chr9:105492165
|
T | A | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+7663T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492165 | ||||||
| chr9:105492221
|
T | A | 1 | a0001c0001t0009g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.586+7719T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492221 | ||||||
| chr9:105492230
|
G | A | 1 | a0001c0001t0004g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.586+7728G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492230 | ||||||
| chr9:105492265
|
T | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+7763T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492265 | ||||||
| chr9:105492272
|
C | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+7770C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492272 | ||||||
| chr9:105492276
|
T | G | 1 | a0001c0001t0004g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586+7774T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492276 | ||||||
| chr9:105492315
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.586+7813G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492315 | ||||||
| chr9:105492361
|
T | C | 1 | a0001c0001t0002g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.586+7859T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492361 | ||||||
| chr9:105492367
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7865T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492367 | ||||||
| chr9:105492388
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7886T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492388 | ||||||
| chr9:105492450
|
G | C | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+7948G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492450 | ||||||
| chr9:105492511
|
T | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+8009T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492511 | ||||||
| chr9:105492575
|
C | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+8073C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492575 | ||||||
| chr9:105492596
|
T | C | 2 | a0001c0002t0010g0105a0001c0002t0010g0110 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.586+8094T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492596 | ||||||
| chr9:105492616
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8114T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492616 | ||||||
| chr9:105492624
|
C | G | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.586+8122C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492624 | ||||||
| chr9:105492742
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8240G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492742 | ||||||
| chr9:105492754
|
T | C | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8252T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492754 | ||||||
| chr9:105492818
|
G | T | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.586+8316G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492818 | ||||||
| chr9:105492881
|
C | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+8379C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492881 | ||||||
| chr9:105492884
|
A | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+8382A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492884 | ||||||
| chr9:105492886
|
A | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+8384A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105492886 | ||||||
| chr9:105493022
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586+8520G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493022 | ||||||
| chr9:105493048
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+8546A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493048 | ||||||
| chr9:105493071
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.586+8569C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493071 | ||||||
| chr9:105493076
|
A | T | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.586+8574A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493076 | ||||||
| chr9:105493086
|
T | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8584T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493086 | ||||||
| chr9:105493120
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8618A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493120 | ||||||
| chr9:105493209
|
G | T | 1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.586+8707G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493209 | ||||||
| chr9:105493220
|
C | T | 1 | a0001c0001t0009g0188 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586+8718C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493220 | ||||||
| chr9:105493300
|
T | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+8798T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493300 | ||||||
| chr9:105493308
|
A | G | 1 | a0001c0001t0018g0330 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.586+8806A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493308 | ||||||
| chr9:105493336
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8834A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493336 | ||||||
| chr9:105493344
|
A | G | 1 | a0001c0001t0024g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.586+8842A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493344 | ||||||
| chr9:105493356
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8854C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493356 | ||||||
| chr9:105493357
|
A | G | 1 | a0001c0001t0004g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.586+8855A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493357 | ||||||
| chr9:105493396
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8894C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493396 | ||||||
| chr9:105493401
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.586+8899C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493401 | ||||||
| chr9:105493402
|
G | A | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.586+8900G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493402 | ||||||
| chr9:105493415
|
C | T | 4 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0050others(1): Show | 4 | HG02074.hp1 HG04184.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+8913C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493415 | ||||||
| chr9:105493449
|
T | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+8947T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493449 | ||||||
| chr9:105493468
|
T | C | 3 | a0001c0001t0022g0170a0001c0001t0022g0173a0001c0001t0032g0163 | 3 | HG02615.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.586+8966T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493468 | ||||||
| chr9:105493542
|
T | G | 63 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(60): Show | 64 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.586+9040T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493542 | ||||||
| chr9:105493556
|
G | C | 1 | a0001c0001t0002g0017 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.586+9054G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493556 | ||||||
| chr9:105493567
|
C | T | 1 | a0001c0001t0042g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.586+9065C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493567 | ||||||
| chr9:105493593
|
C | T | 1 | a0001c0001t0003g0375 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.586+9091C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493593 | ||||||
| chr9:105493597
|
G | A | 1 | a0001c0001t0004g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.586+9095G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493597 | ||||||
| chr9:105493638
|
C | G | 1 | a0001c0001t0001g0002 | 2 | NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.586+9136C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493638 | ||||||
| chr9:105493661
|
C | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+9159C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493661 | ||||||
| chr9:105493703
|
C | G | 264 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.586+9201C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493703 | ||||||
| chr9:105493727
|
C | T | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+9225C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493727 | ||||||
| chr9:105493740
|
T | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+9238T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493740 | ||||||
| chr9:105493869
|
C | A | 1 | a0001c0001t0005g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.586+9367C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493869 | ||||||
| chr9:105493869
|
C | T | 3 | a0001c0001t0009g0191a0001c0001t0009g0197a0001c0001t0009g0198 | 3 | HG00323.hp2 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.586+9367C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493869 | ||||||
| chr9:105493881
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0280 | 2 | HG00621.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.586+9379G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105493881 | ||||||
| chr9:105494120
|
C | T | 1 | a0001c0001t0008g0297 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.586+9618C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494120 | ||||||
| chr9:105494140
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.586+9638A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494140 | ||||||
| chr9:105494147
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+9645A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494147 | ||||||
| chr9:105494262
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+9760T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494262 | ||||||
| chr9:105494263
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+9761G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494263 | ||||||
| chr9:105494288
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0252 | 2 | NA19068.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.586+9786T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494288 | ||||||
| chr9:105494321
|
G | A | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.586+9819G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494321 | ||||||
| chr9:105494329
|
C | T | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.586+9827C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494329 | ||||||
| chr9:105494506
|
A | C | 2 | a0001c0001t0005g0176a0001c0001t0005g0177 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.586+10004A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494506 | ||||||
| chr9:105494743
|
T | G | 265 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(262): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.586+10241T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494743 | ||||||
| chr9:105494747
|
A | G | 77 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(74): Show | 78 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.586+10245A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494747 | ||||||
| chr9:105494766
|
T | C | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.586+10264T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494766 | ||||||
| chr9:105494768
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18966.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.586+10266C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494768 | ||||||
| chr9:105494796
|
C | T | 1 | a0001c0001t0005g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586+10294C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494796 | ||||||
| chr9:105494828
|
C | T | 1 | a0001c0001t0042g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.586+10326C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494828 | ||||||
| chr9:105494831
|
A | C | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+10329A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494831 | ||||||
| chr9:105494848
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10346C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494848 | ||||||
| chr9:105494907
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586+10405C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494907 | ||||||
| chr9:105494918
|
G | C | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586+10416G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494918 | ||||||
| chr9:105494919
|
G | T | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.586+10417G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494919 | ||||||
| chr9:105494983
|
T | C | 374 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.586+10481T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105494983 | ||||||
| chr9:105495037
|
T | TCAGA | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10538_586+1053 others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105495037 | |||||
| chr9:105495073
|
T | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+10571T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495073 | ||||||
| chr9:105495154
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.586+10652C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495154 | ||||||
| chr9:105495159
|
T | C | 266 | a0001c0001t0001g0235a0001c0001t0002g0006a0001c0001t0002g0007others(263): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.586+10657T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495159 | ||||||
| chr9:105495168
|
C | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10666C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495168 | ||||||
| chr9:105495184
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10682C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495184 | ||||||
| chr9:105495217
|
C | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+10715C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495217 | ||||||
| chr9:105495287
|
T | C | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.586+10785T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495287 | ||||||
| chr9:105495307
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10805G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495307 | ||||||
| chr9:105495318
|
A | G | 1 | a0001c0001t0041g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.586+10816A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495318 | ||||||
| chr9:105495324
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+10822C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495324 | ||||||
| chr9:105495350
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.586+10848G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495350 | ||||||
| chr9:105495364
|
TTGGGGTG others(4): Show |
T | 1 | a0001c0001t0041g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.586+10865_586+1087 others(15): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105495364 | |||||
| chr9:105495446
|
C | A | 2 | a0001c0001t0020g0368a0001c0001t0020g0369 | 2 | HG01361.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.586+10944C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495446 | ||||||
| chr9:105495470
|
C | T | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.587-10929C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495470 | ||||||
| chr9:105495474
|
C | A | 1 | a0001c0001t0007g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.587-10925C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495474 | ||||||
| chr9:105495486
|
G | A | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.587-10913G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495486 | ||||||
| chr9:105495487
|
T | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-10912T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495487 | ||||||
| chr9:105495558
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.587-10841C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495558 | ||||||
| chr9:105495572
|
G | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-10827G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495572 | ||||||
| chr9:105495653
|
G | A | 34 | a0001c0001t0002g0066a0001c0001t0003g0324a0001c0001t0003g0336others(31): Show | 34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.587-10746G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495653 | ||||||
| chr9:105495699
|
G | A | 1 | a0001c0001t0003g0342 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.587-10700G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495699 | ||||||
| chr9:105495702
|
C | T | 63 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(60): Show | 64 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.587-10697C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495702 | ||||||
| chr9:105495715
|
G | A | 1 | a0001c0001t0005g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587-10684G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495715 | ||||||
| chr9:105495742
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10657C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495742 | ||||||
| chr9:105495752
|
A | G | 6 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(3): Show | 6 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-10647A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495752 | ||||||
| chr9:105495753
|
G | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10646G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495753 | ||||||
| chr9:105495887
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10512G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495887 | ||||||
| chr9:105495896
|
C | T | 3 | a0001c0001t0022g0170a0001c0001t0022g0173a0001c0001t0032g0163 | 3 | HG02615.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-10503C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105495896 | ||||||
| chr9:105495969
|
TA | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(37): Show | 41 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.587-10414delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105495969 | |||||
| chr9:105496003
|
A | G | 1 | a0002c0004t0029g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.587-10396A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496003 | ||||||
| chr9:105496071
|
C | G | 100 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.587-10328C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496071 | ||||||
| chr9:105496078
|
A | G | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-10321A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496078 | ||||||
| chr9:105496079
|
G | C | 1 | a0001c0001t0003g0324 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.587-10320G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496079 | ||||||
| chr9:105496125
|
C | G | 1 | a0001c0001t0022g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.587-10274C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496125 | ||||||
| chr9:105496157
|
C | A | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-10242C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496157 | ||||||
| chr9:105496178
|
A | C | 1 | a0001c0001t0002g0017 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.587-10221A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496178 | ||||||
| chr9:105496185
|
G | C | 126 | a0001c0001t0002g0066a0001c0001t0003g0005a0001c0001t0003g0236others(123): Show | 128 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.587-10214G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496185 | ||||||
| chr9:105496202
|
C | CT | 88 | a0001c0001t0001g0204a0001c0001t0001g0252a0001c0001t0001g0253others(85): Show | 89 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.587-10178dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105496202 | |||||
| chr9:105496202
|
CT | C | 13 | a0001c0001t0002g0053a0001c0001t0004g0115a0001c0001t0005g0178others(10): Show | 13 | HG00099.hp1 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.587-10178delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105496202 | |||||
| chr9:105496202
|
CTT | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.587-10179_587-1017 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105496202 | |||||
| chr9:105496209
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10190T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496209 | ||||||
| chr9:105496222
|
G | T | 1 | a0001c0001t0002g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-10177G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496222 | ||||||
| chr9:105496268
|
ATC | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10125_587-1012 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105496268 | |||||
| chr9:105496279
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.587-10120C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496279 | ||||||
| chr9:105496280
|
A | G | 1 | a0001c0001t0009g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.587-10119A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496280 | ||||||
| chr9:105496291
|
C | T | 43 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(40): Show | 44 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.587-10108C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496291 | ||||||
| chr9:105496358
|
C | T | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-10041C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496358 | ||||||
| chr9:105496362
|
G | C | 1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.587-10037G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496362 | ||||||
| chr9:105496449
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-9950T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496449 | ||||||
| chr9:105496541
|
A | T | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-9858A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496541 | ||||||
| chr9:105496704
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.587-9695A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496704 | ||||||
| chr9:105496719
|
A | T | 101 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.587-9680A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496719 | ||||||
| chr9:105496943
|
A | G | 2 | a0001c0001t0005g0171a0001c0001t0005g0172 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.587-9456A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496943 | ||||||
| chr9:105496981
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-9418A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105496981 | ||||||
| chr9:105497187
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.587-9212C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497187 | ||||||
| chr9:105497191
|
C | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-9208C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497191 | ||||||
| chr9:105497198
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-9201G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497198 | ||||||
| chr9:105497263
|
T | C | 1 | a0001c0001t0007g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.587-9136T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497263 | ||||||
| chr9:105497267
|
T | TA | 266 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(263): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.587-9131dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105497267 | |||||
| chr9:105497301
|
T | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-9098T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497301 | ||||||
| chr9:105497304
|
G | A | 1 | a0001c0001t0039g0279 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.587-9095G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497304 | ||||||
| chr9:105497368
|
C | T | 1 | a0001c0001t0003g0324 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.587-9031C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497368 | ||||||
| chr9:105497382
|
A | T | 265 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(262): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.587-9017A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497382 | ||||||
| chr9:105497433
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.587-8966A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497433 | ||||||
| chr9:105497495
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.587-8904G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497495 | ||||||
| chr9:105497572
|
T | C | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-8827T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497572 | ||||||
| chr9:105497588
|
C | G | 1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587-8811C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497588 | ||||||
| chr9:105497622
|
G | T | 1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587-8777G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497622 | ||||||
| chr9:105497640
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.587-8759A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497640 | ||||||
| chr9:105497749
|
G | A | 1 | a0001c0001t0026g0012 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.587-8650G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497749 | ||||||
| chr9:105497801
|
T | C | 3 | a0001c0001t0022g0170a0001c0001t0022g0173a0001c0001t0032g0163 | 3 | HG02615.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-8598T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497801 | ||||||
| chr9:105497982
|
T | C | 1 | a0001c0001t0024g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.587-8417T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105497982 | ||||||
| chr9:105498008
|
T | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8391T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498008 | ||||||
| chr9:105498053
|
T | C | 2 | a0001c0001t0019g0258a0001c0001t0019g0294 | 2 | NA18954.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.587-8346T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498053 | ||||||
| chr9:105498091
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8308C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498091 | ||||||
| chr9:105498121
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8278A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498121 | ||||||
| chr9:105498122
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8277G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498122 | ||||||
| chr9:105498179
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8220C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498179 | ||||||
| chr9:105498190
|
T | TTTA | 46 | a0001c0001t0001g0240a0001c0001t0001g0253a0001c0001t0001g0263others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.587-8176_587-8174d others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
T | TTTATTA | 28 | a0001c0001t0001g0266a0001c0001t0001g0270a0001c0001t0001g0273others(25): Show | 29 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.587-8179_587-8174d others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
T | TTTATTAT others(2): Show |
22 | a0001c0001t0001g0216a0001c0001t0004g0106a0001c0001t0004g0109others(19): Show | 22 | HG00597.hp1 HG00735.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.587-8182_587-8174d others(11): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
T | TTTATTAT others(5): Show |
9 | a0001c0001t0004g0104a0001c0001t0004g0112a0001c0001t0004g0115others(6): Show | 9 | HG00099.hp1 HG01192.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.587-8185_587-8174d others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
TTTA | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8176_587-8174d others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
TTTATTA | T | 9 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(6): Show | 9 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-8179_587-8174d others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498190
|
TTTATTAT others(2): Show |
T | 102 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.587-8182_587-8174d others(11): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498190 | |||||
| chr9:105498223
|
A | ATTATTAT others(11): Show |
4 | a0001c0001t0003g0337a0001c0001t0003g0355a0001c0001t0003g0356others(1): Show | 4 | NA18954.hp2 NA18961.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-8174_587-8173i others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498223 | |||||
| chr9:105498223
|
A | ATTATTAT others(8): Show |
28 | a0001c0001t0003g0005a0001c0001t0003g0320a0001c0001t0003g0322others(25): Show | 29 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.587-8174_587-8173i others(17): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498223 | |||||
| chr9:105498223
|
A | ATTATTAT others(5): Show |
15 | a0001c0001t0003g0318a0001c0001t0003g0321a0001c0001t0003g0331others(12): Show | 15 | HG01167.hp2 HG01515.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-8174_587-8173i others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498223 | |||||
| chr9:105498223
|
A | ATTATTAT others(5): Show |
1 | a0001c0001t0015g0327 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.587-8174_587-8173i others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498223 | |||||
| chr9:105498223
|
A | ATTG | 11 | a0001c0001t0006g0086a0001c0001t0006g0334a0001c0001t0006g0341others(8): Show | 11 | HG01261.hp2 HG01361.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-8173_587-8171d others(5): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105498223 | |||||
| chr9:105498296
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.587-8103C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498296 | ||||||
| chr9:105498584
|
A | C | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.587-7815A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498584 | ||||||
| chr9:105498755
|
A | G | 8 | a0001c0001t0003g0322a0001c0001t0003g0323a0001c0001t0003g0325others(5): Show | 8 | HG00673.hp1 HG03927.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-7644A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498755 | ||||||
| chr9:105498852
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-7547C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498852 | ||||||
| chr9:105498907
|
C | G | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-7492C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498907 | ||||||
| chr9:105498908
|
G | A | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-7491G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105498908 | ||||||
| chr9:105499143
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-7256A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499143 | ||||||
| chr9:105499214
|
C | T | 2 | a0001c0001t0011g0314a0001c0001t0011g0315 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.587-7185C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499214 | ||||||
| chr9:105499250
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 7 | NA18747.hp1 NA18966.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-7149A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499250 | ||||||
| chr9:105499325
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 7 | NA18747.hp1 NA18966.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-7074A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499325 | ||||||
| chr9:105499380
|
T | C | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.587-7019T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499380 | ||||||
| chr9:105499443
|
C | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-6956C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499443 | ||||||
| chr9:105499655
|
G | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.587-6744G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499655 | ||||||
| chr9:105499823
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.587-6576C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499823 | ||||||
| chr9:105499878
|
A | G | 103 | a0001c0001t0001g0085a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 104 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.587-6521A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105499878 | ||||||
| chr9:105500045
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-6354G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500045 | ||||||
| chr9:105500062
|
C | A | 2 | a0001c0001t0022g0173a0001c0001t0032g0163 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-6337C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500062 | ||||||
| chr9:105500072
|
T | A | 2 | a0002c0004t0002g0016a0002c0004t0029g0074 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587-6327T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500072 | ||||||
| chr9:105500305
|
T | C | 2 | a0001c0001t0004g0127a0001c0001t0004g0130 | 2 | NA18948.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.587-6094T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500305 | ||||||
| chr9:105500325
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.587-6074G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500325 | ||||||
| chr9:105500408
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-5991A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500408 | ||||||
| chr9:105500416
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.587-5983G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500416 | ||||||
| chr9:105500462
|
G | A | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.587-5937G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500462 | ||||||
| chr9:105500490
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587-5909C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500490 | ||||||
| chr9:105500589
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.587-5810A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500589 | ||||||
| chr9:105500663
|
C | T | 1 | a0001c0001t0023g0339 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.587-5736C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500663 | ||||||
| chr9:105500784
|
A | G | 3 | a0001c0001t0008g0304a0001c0001t0008g0305a0001c0001t0008g0306 | 3 | NA18959.hp2 NA18993.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.587-5615A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500784 | ||||||
| chr9:105500896
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.587-5503T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500896 | ||||||
| chr9:105500929
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.587-5470A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105500929 | ||||||
| chr9:105501204
|
A | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.587-5195A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501204 | ||||||
| chr9:105501210
|
A | C | 12 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(9): Show | 12 | HG00140.hp1 HG00735.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-5189A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501210 | ||||||
| chr9:105501224
|
G | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-5175G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501224 | ||||||
| chr9:105501227
|
AT | A | 11 | a0001c0001t0003g0318a0001c0001t0012g0098a0001c0001t0012g0099others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-5161delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105501227 | |||||
| chr9:105501280
|
G | T | 4 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0174others(1): Show | 4 | HG00280.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-5119G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501280 | ||||||
| chr9:105501460
|
A | G | 5 | a0001c0001t0006g0341a0001c0001t0006g0346a0001c0001t0006g0347others(2): Show | 5 | HG01261.hp2 HG02148.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-4939A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501460 | ||||||
| chr9:105501464
|
C | G | 1 | a0001c0001t0004g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.587-4935C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501464 | ||||||
| chr9:105501568
|
G | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-4831G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501568 | ||||||
| chr9:105501570
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0043a0001c0001t0002g0059 | 3 | HG00621.hp1 HG02074.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.587-4829A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501570 | ||||||
| chr9:105501596
|
A | AT | 6 | a0001c0001t0001g0210a0001c0001t0001g0237a0001c0001t0001g0243others(3): Show | 6 | HG02056.hp1 HG02970.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-4786dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105501596 | |||||
| chr9:105501596
|
AT | A | 153 | a0001c0001t0002g0067a0001c0001t0003g0005a0001c0001t0003g0318others(150): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.587-4786delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105501596 | |||||
| chr9:105501626
|
A | G | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.587-4773A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501626 | ||||||
| chr9:105501743
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4656G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501743 | ||||||
| chr9:105501744
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0090 | 2 | NA19004.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.587-4655C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501744 | ||||||
| chr9:105501910
|
C | T | 1 | a0001c0001t0024g0254 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.587-4489C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501910 | ||||||
| chr9:105501912
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4487A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501912 | ||||||
| chr9:105501932
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-4467A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105501932 | ||||||
| chr9:105502037
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0286 | 2 | NA18942.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.587-4362C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502037 | ||||||
| chr9:105502109
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4290G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502109 | ||||||
| chr9:105502212
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4187A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502212 | ||||||
| chr9:105502314
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.587-4085G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502314 | ||||||
| chr9:105502422
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587-3977G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502422 | ||||||
| chr9:105502440
|
A | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3959A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502440 | ||||||
| chr9:105502500
|
G | A | 263 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.587-3899G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502500 | ||||||
| chr9:105502521
|
C | T | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-3878C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502521 | ||||||
| chr9:105502635
|
A | G | 1 | a0001c0001t0005g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.587-3764A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502635 | ||||||
| chr9:105502666
|
A | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0065a0001c0001t0005g0176others(1): Show | 4 | HG02630.hp2 HG03130.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3733A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502666 | ||||||
| chr9:105502671
|
A | T | 2 | a0001c0003t0003g0332a0001c0003t0003g0333 | 2 | NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.587-3728A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502671 | ||||||
| chr9:105502689
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3710G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502689 | ||||||
| chr9:105502731
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-3668A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502731 | ||||||
| chr9:105502884
|
A | AT | 29 | a0001c0001t0001g0230a0001c0001t0001g0257a0001c0001t0001g0265others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.587-3497dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105502884 | |||||
| chr9:105502884
|
AT | A | 109 | a0001c0001t0001g0217a0001c0001t0001g0229a0001c0001t0002g0006others(106): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.587-3497delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105502884 | |||||
| chr9:105502923
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3476T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105502923 | ||||||
| chr9:105503009
|
C | T | 1 | a0001c0001t0041g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.587-3390C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503009 | ||||||
| chr9:105503031
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.587-3368C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503031 | ||||||
| chr9:105503103
|
G | T | 1 | a0001c0001t0004g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587-3296G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503103 | ||||||
| chr9:105503326
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3073A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503326 | ||||||
| chr9:105503595
|
T | C | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.587-2804T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503595 | ||||||
| chr9:105503765
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.587-2634C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503765 | ||||||
| chr9:105503793
|
C | T | 2 | a0001c0001t0011g0312a0001c0001t0011g0313 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.587-2606C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503793 | ||||||
| chr9:105503801
|
C | T | 1 | a0001c0001t0013g0097 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.587-2598C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105503801 | ||||||
| chr9:105504078
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-2321A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105504078 | ||||||
| chr9:105504400
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1999A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105504400 | ||||||
| chr9:105504621
|
A | T | 1 | a0001c0001t0004g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587-1778A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105504621 | ||||||
| chr9:105504698
|
C | CT | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1698dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr9 | 105504698 | |||||
| chr9:105504901
|
G | A | 1 | a0001c0001t0005g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.587-1498G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105504901 | ||||||
| chr9:105504972
|
A | G | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-1427A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105504972 | ||||||
| chr9:105505096
|
T | C | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-1303T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505096 | ||||||
| chr9:105505177
|
G | A | 76 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(73): Show | 77 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.587-1222G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505177 | ||||||
| chr9:105505256
|
G | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.587-1143G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505256 | ||||||
| chr9:105505349
|
C | G | 5 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0056others(2): Show | 5 | NA18747.hp2 NA18970.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-1050C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505349 | ||||||
| chr9:105505402
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-997T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505402 | ||||||
| chr9:105505426
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-973A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505426 | ||||||
| chr9:105505642
|
T | A | 1 | a0001c0001t0004g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.587-757T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505642 | ||||||
| chr9:105505652
|
C | A | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-747C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505652 | ||||||
| chr9:105505815
|
C | T | 1 | a0001c0001t0004g0114 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.587-584C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105505815 | ||||||
| chr9:105506155
|
A | AG | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-244_587-243ins others(1): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105506155 | ||||||
| chr9:105506306
|
G | A | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-93G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 7/13 | chr9 | 105506306 | ||||||
| chr9:105506857
|
C | T | 5 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(2): Show | 5 | HG01891.hp1 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.796+249C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105506857 | ||||||
| chr9:105506888
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+280C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105506888 | ||||||
| chr9:105506919
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+311A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105506919 | ||||||
| chr9:105507030
|
G | A | 37 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.796+422G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507030 | ||||||
| chr9:105507153
|
T | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+545T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507153 | ||||||
| chr9:105507198
|
C | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(369): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.796+590C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507198 | ||||||
| chr9:105507231
|
C | T | 2 | a0001c0001t0005g0176a0001c0001t0005g0177 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.796+623C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507231 | ||||||
| chr9:105507312
|
T | C | 2 | a0001c0001t0005g0159a0001c0001t0005g0162 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.796+704T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507312 | ||||||
| chr9:105507362
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.796+754G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507362 | ||||||
| chr9:105507539
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+931G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507539 | ||||||
| chr9:105507856
|
CATGATTC others(5): Show |
C | 1 | a0001c0001t0015g0340 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.797-758_797-747del others(12): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105507856 | |||||
| chr9:105507888
|
TC | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.797-728delC | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507888 | ||||||
| chr9:105507889
|
C | T | 1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.797-728C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507889 | ||||||
| chr9:105507889
|
CT | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(137): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.797-709delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105507889 | |||||
| chr9:105507889
|
CTT | C | 211 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(208): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.797-710_797-709del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105507889 | |||||
| chr9:105507933
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.797-684C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105507933 | ||||||
| chr9:105508026
|
C | T | 1 | a0001c0001t0013g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.797-591C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508026 | ||||||
| chr9:105508057
|
C | T | 1 | a0001c0001t0005g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.797-560C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508057 | ||||||
| chr9:105508074
|
G | A | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.797-543G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508074 | ||||||
| chr9:105508160
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.797-457G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508160 | ||||||
| chr9:105508174
|
C | CT | 14 | a0001c0001t0001g0210a0001c0001t0001g0265a0001c0001t0002g0028others(11): Show | 14 | HG01433.hp1 HG01891.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.797-422dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105508174 | |||||
| chr9:105508174
|
CT | C | 75 | a0001c0001t0002g0007a0001c0001t0002g0031a0001c0001t0003g0358others(72): Show | 76 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.797-422delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105508174 | |||||
| chr9:105508174
|
CTT | C | 71 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(68): Show | 72 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.797-423_797-422del others(2): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr9 | 105508174 | |||||
| chr9:105508239
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.797-378G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508239 | ||||||
| chr9:105508268
|
C | T | 1 | a0001c0001t0033g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.797-349C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508268 | ||||||
| chr9:105508327
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.797-290G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508327 | ||||||
| chr9:105508394
|
G | T | 1 | a0001c0001t0006g0345 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.797-223G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508394 | ||||||
| chr9:105508412
|
T | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-205T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508412 | ||||||
| chr9:105508420
|
G | A | 2 | a0001c0001t0018g0329a0001c0001t0018g0330 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.797-197G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508420 | ||||||
| chr9:105508446
|
G | A | 1 | a0001c0001t0005g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.797-171G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508446 | ||||||
| chr9:105508469
|
G | A | 43 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(40): Show | 44 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.797-148G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508469 | ||||||
| chr9:105508554
|
C | G | 1 | a0001c0001t0002g0066 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.797-63C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508554 | ||||||
| chr9:105508607
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-10G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508607 | ||||||
| chr9:105508611
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.797-6C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 8/13 | chr9 | 105508611 | ||||||
| chr9:105508890
|
ATTGGGTT others(4): Show |
A | 1 | a0001c0001t0004g0135 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.895+177_895+187del others(11): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105508890 | |||||
| chr9:105509107
|
T | C | 1 | a0001c0001t0035g0232 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.895+392T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509107 | ||||||
| chr9:105509223
|
T | C | 2 | a0001c0001t0004g0144a0001c0001t0005g0158 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.895+508T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509223 | ||||||
| chr9:105509350
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+635C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509350 | ||||||
| chr9:105509369
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+654T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509369 | ||||||
| chr9:105509424
|
G | A | 2 | a0001c0001t0003g0323a0001c0001t0003g0335 | 2 | NA19004.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.895+709G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509424 | ||||||
| chr9:105509519
|
C | T | 1 | a0001c0002t0010g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.895+804C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509519 | ||||||
| chr9:105509621
|
G | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.895+906G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509621 | ||||||
| chr9:105509630
|
CA | C | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.895+923delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105509630 | |||||
| chr9:105509838
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+1123T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509838 | ||||||
| chr9:105509970
|
G | A | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.895+1255G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509970 | ||||||
| chr9:105509978
|
T | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.895+1263T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105509978 | ||||||
| chr9:105510218
|
A | G | 2 | a0001c0003t0003g0332a0001c0003t0003g0333 | 2 | NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.895+1503A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510218 | ||||||
| chr9:105510250
|
G | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.895+1535G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510250 | ||||||
| chr9:105510258
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.895+1543T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510258 | ||||||
| chr9:105510291
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.895+1576A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510291 | ||||||
| chr9:105510320
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0005g0158 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.895+1605A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510320 | ||||||
| chr9:105510331
|
C | T | 3 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.895+1616C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510331 | ||||||
| chr9:105510332
|
TC | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.895+1619delC | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105510332 | |||||
| chr9:105510400
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+1685G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510400 | ||||||
| chr9:105510514
|
T | C | 1 | a0001c0001t0013g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.895+1799T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510514 | ||||||
| chr9:105510518
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.895+1803C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510518 | ||||||
| chr9:105510595
|
G | T | 5 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+1880G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510595 | ||||||
| chr9:105510618
|
A | C | 102 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.895+1903A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510618 | ||||||
| chr9:105510851
|
C | T | 16 | a0001c0001t0005g0146a0001c0001t0005g0157a0001c0001t0005g0159others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.896-1956C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510851 | ||||||
| chr9:105510988
|
C | CT | 37 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(34): Show | 38 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.896-1805dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105510988 | |||||
| chr9:105510991
|
T | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-1816T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105510991 | ||||||
| chr9:105511019
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-1788C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511019 | ||||||
| chr9:105511042
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-1765A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511042 | ||||||
| chr9:105511057
|
T | C | 4 | a0001c0001t0003g0337a0001c0001t0003g0342a0001c0001t0003g0356others(1): Show | 4 | NA18945.hp1 NA18954.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-1750T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511057 | ||||||
| chr9:105511126
|
C | G | 2 | a0001c0001t0011g0312a0001c0001t0011g0313 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.896-1681C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511126 | ||||||
| chr9:105511192
|
A | AT | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(105): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.896-1603dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105511192 | |||||
| chr9:105511192
|
A | ATT | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0038others(3): Show | 6 | NA18963.hp2 NA18991.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.896-1604_896-1603d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105511192 | |||||
| chr9:105511237
|
T | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-1570T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511237 | ||||||
| chr9:105511411
|
T | C | 4 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0050others(1): Show | 4 | HG02074.hp1 HG04184.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-1396T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511411 | ||||||
| chr9:105511986
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.896-821G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105511986 | ||||||
| chr9:105512086
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.896-721A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512086 | ||||||
| chr9:105512171
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.896-636A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512171 | ||||||
| chr9:105512228
|
T | TC | 266 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(263): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.896-579_896-578ins others(1): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512228 | ||||||
| chr9:105512229
|
T | C | 266 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(263): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.896-578T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512229 | ||||||
| chr9:105512249
|
C | T | 1 | a0001c0001t0009g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.896-558C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512249 | ||||||
| chr9:105512331
|
GA | G | 4 | a0001c0001t0004g0001a0001c0001t0004g0107a0001c0001t0004g0111others(1): Show | 5 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.896-473delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105512331 | |||||
| chr9:105512488
|
A | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.896-319A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512488 | ||||||
| chr9:105512650
|
A | G | 228 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(225): Show | 231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.896-157A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512650 | ||||||
| chr9:105512678
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.896-129A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | chr9 | 105512678 | ||||||
| chr9:105512732
|
TGTG | T | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.896-71_896-69delGT others(1): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr9 | 105512732 | |||||
| chr9:105513129
|
T | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+193T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513129 | ||||||
| chr9:105513299
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+363G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513299 | ||||||
| chr9:105513340
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+404A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513340 | ||||||
| chr9:105513404
|
TAA | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+470_1025+471d others(4): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105513404 | |||||
| chr9:105513446
|
A | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+510A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513446 | ||||||
| chr9:105513465
|
G | A | 5 | a0001c0001t0005g0146a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG01099.hp1 HG01167.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+529G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513465 | ||||||
| chr9:105513496
|
T | C | 374 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0085others(371): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1025+560T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513496 | ||||||
| chr9:105513687
|
T | G | 6 | a0001c0001t0009g0188a0001c0001t0009g0190a0001c0001t0009g0191others(3): Show | 6 | HG00323.hp2 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025+751T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513687 | ||||||
| chr9:105513928
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+992A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513928 | ||||||
| chr9:105513956
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1025+1020G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105513956 | ||||||
| chr9:105514012
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1076A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514012 | ||||||
| chr9:105514030
|
A | C | 1 | a0001c0001t0004g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1025+1094A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514030 | ||||||
| chr9:105514048
|
G | A | 1 | a0001c0001t0007g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1025+1112G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514048 | ||||||
| chr9:105514113
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1177G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514113 | ||||||
| chr9:105514189
|
C | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+1253C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514189 | ||||||
| chr9:105514326
|
T | C | 102 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(99): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1025+1390T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514326 | ||||||
| chr9:105514379
|
C | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0132 | 3 | HG01243.hp2 HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1025+1443C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514379 | ||||||
| chr9:105514423
|
T | C | 281 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(278): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1025+1487T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514423 | ||||||
| chr9:105514517
|
T | C | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+1581T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514517 | ||||||
| chr9:105514721
|
C | G | 1 | a0001c0001t0002g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1025+1785C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514721 | ||||||
| chr9:105514948
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2012C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514948 | ||||||
| chr9:105514950
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2014G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105514950 | ||||||
| chr9:105515057
|
C | T | 1 | a0001c0001t0035g0232 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1025+2121C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515057 | ||||||
| chr9:105515093
|
C | A | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+2157C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515093 | ||||||
| chr9:105515104
|
C | T | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1025+2168C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515104 | ||||||
| chr9:105515142
|
C | T | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1025+2206C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515142 | ||||||
| chr9:105515143
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+2207G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515143 | ||||||
| chr9:105515156
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2220C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515156 | ||||||
| chr9:105515194
|
C | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2258C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515194 | ||||||
| chr9:105515208
|
C | T | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2272C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515208 | ||||||
| chr9:105515236
|
G | A | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(12): Show | 15 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1025+2300G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515236 | ||||||
| chr9:105515252
|
C | T | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1025+2316C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515252 | ||||||
| chr9:105515323
|
C | T | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1025+2387C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515323 | ||||||
| chr9:105515486
|
T | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+2550T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515486 | ||||||
| chr9:105515529
|
A | G | 1 | a0001c0001t0013g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1025+2593A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515529 | ||||||
| chr9:105515646
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1025+2710C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515646 | ||||||
| chr9:105515660
|
C | G | 5 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2724C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515660 | ||||||
| chr9:105515691
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2755T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515691 | ||||||
| chr9:105515787
|
G | GTT | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2851_1025+285 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515787 | ||||||
| chr9:105515788
|
G | GT | 123 | a0001c0001t0001g0222a0001c0001t0001g0235a0001c0001t0001g0248others(120): Show | 124 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1025+2867dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105515788 | |||||
| chr9:105515788
|
G | GTT | 10 | a0001c0001t0002g0019a0001c0001t0002g0032a0001c0001t0002g0035others(7): Show | 10 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+2866_1025+286 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105515788 | |||||
| chr9:105515788
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2852G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515788 | ||||||
| chr9:105515789
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1025+2853T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105515789 | ||||||
| chr9:105516186
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3250G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516186 | ||||||
| chr9:105516220
|
C | T | 1 | a0001c0001t0003g0338 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1025+3284C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516220 | ||||||
| chr9:105516236
|
C | G | 1 | a0001c0001t0014g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1025+3300C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516236 | ||||||
| chr9:105516238
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1025+3302G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516238 | ||||||
| chr9:105516288
|
C | A | 1 | a0001c0001t0002g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1025+3352C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516288 | ||||||
| chr9:105516402
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025+3466C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516402 | ||||||
| chr9:105516421
|
A | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3485A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516421 | ||||||
| chr9:105516523
|
C | G | 8 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0217others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+3587C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516523 | ||||||
| chr9:105516528
|
G | A | 1 | a0001c0001t0013g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1025+3592G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516528 | ||||||
| chr9:105516805
|
A | C | 1 | a0001c0001t0002g0008 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1025+3869A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516805 | ||||||
| chr9:105516878
|
A | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+3942A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516878 | ||||||
| chr9:105516985
|
C | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+4049C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105516985 | ||||||
| chr9:105517017
|
T | C | 1 | a0001c0001t0017g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1025+4081T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517017 | ||||||
| chr9:105517078
|
C | G | 280 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(277): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1025+4142C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517078 | ||||||
| chr9:105517137
|
T | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+4201T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517137 | ||||||
| chr9:105517264
|
G | A | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1025+4328G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517264 | ||||||
| chr9:105517404
|
C | T | 1 | a0001c0001t0023g0319 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1025+4468C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517404 | ||||||
| chr9:105517738
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0302 | 2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1025+4802C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517738 | ||||||
| chr9:105517749
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+4813C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517749 | ||||||
| chr9:105517952
|
A | G | 2 | a0001c0003t0003g0332a0001c0003t0003g0333 | 2 | NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1025+5016A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517952 | ||||||
| chr9:105517970
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1025+5034A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517970 | ||||||
| chr9:105517971
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1025+5035C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105517971 | ||||||
| chr9:105518058
|
CAAA | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+5123_1025+512 others(7): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518058 | ||||||
| chr9:105518155
|
A | G | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1025+5219A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518155 | ||||||
| chr9:105518190
|
A | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1025+5254A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518190 | ||||||
| chr9:105518392
|
A | G | 1 | a0001c0001t0005g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1025+5456A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518392 | ||||||
| chr9:105518600
|
T | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+5664T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518600 | ||||||
| chr9:105518630
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+5694T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518630 | ||||||
| chr9:105518631
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+5695G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518631 | ||||||
| chr9:105518635
|
T | C | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+5699T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518635 | ||||||
| chr9:105518661
|
A | G | 3 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122 | 3 | HG02109.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1025+5725A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518661 | ||||||
| chr9:105518913
|
C | A | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1025+5977C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518913 | ||||||
| chr9:105518927
|
A | G | 225 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(222): Show | 227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1025+5991A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518927 | ||||||
| chr9:105518972
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+6036G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105518972 | ||||||
| chr9:105519009
|
A | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+6073A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519009 | ||||||
| chr9:105519085
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+6149C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519085 | ||||||
| chr9:105519167
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1025+6231C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519167 | ||||||
| chr9:105519201
|
TCA | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+6268_1025+626 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105519201 | |||||
| chr9:105519238
|
G | T | 13 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1025+6302G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519238 | ||||||
| chr9:105519270
|
TA | T | 9 | a0001c0001t0006g0086a0001c0001t0006g0334a0001c0001t0006g0341others(6): Show | 9 | HG01261.hp2 HG02148.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025+6341delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105519270 | |||||
| chr9:105519419
|
C | T | 5 | a0001c0001t0001g0259a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG01081.hp1 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025+6483C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519419 | ||||||
| chr9:105519598
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+6662C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519598 | ||||||
| chr9:105519662
|
G | C | 1 | a0001c0001t0010g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1025+6726G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519662 | ||||||
| chr9:105519700
|
A | G | 2 | a0001c0001t0022g0173a0001c0001t0032g0163 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1025+6764A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519700 | ||||||
| chr9:105519842
|
G | A | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+6906G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519842 | ||||||
| chr9:105519884
|
A | T | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+6948A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519884 | ||||||
| chr9:105519966
|
G | A | 1 | a0001c0001t0004g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1025+7030G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105519966 | ||||||
| chr9:105520086
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+7150G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520086 | ||||||
| chr9:105520089
|
TGTGGCAG others(5): Show |
T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1025+7173_1025+718 others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105520089 | |||||
| chr9:105520244
|
G | T | 1 | a0001c0001t0020g0368 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1025+7308G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520244 | ||||||
| chr9:105520278
|
C | A | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1025+7342C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520278 | ||||||
| chr9:105520388
|
C | T | 43 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(40): Show | 44 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1025+7452C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520388 | ||||||
| chr9:105520397
|
G | T | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1025+7461G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520397 | ||||||
| chr9:105520409
|
T | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1025+7473T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520409 | ||||||
| chr9:105520411
|
C | CAT | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+7481_1025+748 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105520411 | |||||
| chr9:105520495
|
C | T | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1025+7559C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520495 | ||||||
| chr9:105520574
|
A | G | 226 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(223): Show | 228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1025+7638A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105520574 | ||||||
| chr9:105520585
|
A | AT | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+7652dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105520585 | |||||
| chr9:105521062
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+8126C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521062 | ||||||
| chr9:105521128
|
A | G | 1 | a0001c0001t0003g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1025+8192A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521128 | ||||||
| chr9:105521148
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+8212A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521148 | ||||||
| chr9:105521343
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+8407G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521343 | ||||||
| chr9:105521446
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1025+8510G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521446 | ||||||
| chr9:105521488
|
CAG | C | 7 | a0001c0001t0008g0004a0001c0001t0008g0296a0001c0001t0008g0297others(4): Show | 8 | NA18949.hp1 NA18957.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+8556_1025+855 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105521488 | |||||
| chr9:105521536
|
C | A | 1 | a0001c0001t0002g0089 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1025+8600C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521536 | ||||||
| chr9:105521558
|
A | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+8622A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521558 | ||||||
| chr9:105521671
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1025+8735T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521671 | ||||||
| chr9:105521784
|
A | G | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1025+8848A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521784 | ||||||
| chr9:105521909
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1025+8973T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521909 | ||||||
| chr9:105521949
|
C | T | 3 | a0001c0001t0004g0109a0001c0001t0004g0123a0001c0001t0004g0126 | 3 | HG00741.hp1 HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1025+9013C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521949 | ||||||
| chr9:105521996
|
C | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1025+9060C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105521996 | ||||||
| chr9:105522138
|
A | G | 2 | a0001c0001t0004g0103a0001c0001t0004g0104 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1025+9202A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522138 | ||||||
| chr9:105522247
|
C | T | 1 | a0001c0001t0003g0356 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1025+9311C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522247 | ||||||
| chr9:105522418
|
G | A | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+9482G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522418 | ||||||
| chr9:105522491
|
G | A | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1025+9555G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522491 | ||||||
| chr9:105522536
|
A | G | 1 | a0001c0001t0004g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1025+9600A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522536 | ||||||
| chr9:105522545
|
C | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0015 | 2 | NA18942.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1025+9609C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522545 | ||||||
| chr9:105522789
|
T | C | 10 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(7): Show | 10 | HG01255.hp2 HG02257.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1025+9853T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522789 | ||||||
| chr9:105522998
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+10062C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105522998 | ||||||
| chr9:105523000
|
C | G | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+10064C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523000 | ||||||
| chr9:105523105
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1025+10169C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523105 | ||||||
| chr9:105523325
|
C | T | 4 | a0001c0002t0010g0105a0001c0002t0010g0110a0001c0002t0010g0122others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+10389C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523325 | ||||||
| chr9:105523448
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+10512G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523448 | ||||||
| chr9:105523569
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+10633G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523569 | ||||||
| chr9:105523806
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-10687C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523806 | ||||||
| chr9:105523953
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-10540G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105523953 | ||||||
| chr9:105524025
|
A | C | 1 | a0001c0001t0005g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1026-10468A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524025 | ||||||
| chr9:105524031
|
G | A | 1 | a0001c0001t0014g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1026-10462G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524031 | ||||||
| chr9:105524121
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-10372C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524121 | ||||||
| chr9:105524342
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-10151G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524342 | ||||||
| chr9:105524442
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-10051G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524442 | ||||||
| chr9:105524477
|
C | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1026-10016C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524477 | ||||||
| chr9:105524592
|
A | G | 1 | a0001c0001t0005g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1026-9901A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524592 | ||||||
| chr9:105524623
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-9870C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524623 | ||||||
| chr9:105524682
|
C | T | 1 | a0001c0001t0005g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1026-9811C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524682 | ||||||
| chr9:105524683
|
G | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-9810G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524683 | ||||||
| chr9:105524700
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1026-9793C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524700 | ||||||
| chr9:105524772
|
C | T | 1 | a0001c0001t0007g0202 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1026-9721C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524772 | ||||||
| chr9:105524854
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-9639G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105524854 | ||||||
| chr9:105525050
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026-9443C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525050 | ||||||
| chr9:105525086
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-9407A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525086 | ||||||
| chr9:105525177
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1026-9316C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525177 | ||||||
| chr9:105525365
|
C | T | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-9128C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525365 | ||||||
| chr9:105525367
|
G | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-9126G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525367 | ||||||
| chr9:105525404
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-9089G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525404 | ||||||
| chr9:105525779
|
T | G | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1026-8714T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525779 | ||||||
| chr9:105525786
|
A | AAATCTTT others(326): Show |
1 | a0001c0001t0025g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026-8701_1026-870 others(337): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105525786 | |||||
| chr9:105525855
|
A | G | 3 | a0001c0001t0013g0097a0001c0002t0021g0316a0001c0002t0021g0317 | 3 | HG02257.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-8638A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525855 | ||||||
| chr9:105525892
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-8601A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525892 | ||||||
| chr9:105525933
|
C | G | 1 | a0001c0001t0003g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1026-8560C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105525933 | ||||||
| chr9:105526262
|
T | A | 1 | a0001c0001t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1026-8231T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526262 | ||||||
| chr9:105526424
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-8069G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526424 | ||||||
| chr9:105526487
|
T | C | 8 | a0001c0001t0005g0146a0001c0001t0005g0160a0001c0001t0005g0161others(5): Show | 8 | HG00140.hp1 HG00735.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-8006T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526487 | ||||||
| chr9:105526503
|
G | A | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1026-7990G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526503 | ||||||
| chr9:105526571
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1026-7922T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526571 | ||||||
| chr9:105526601
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1026-7892C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526601 | ||||||
| chr9:105526809
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-7684A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526809 | ||||||
| chr9:105526868
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-7625G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526868 | ||||||
| chr9:105526887
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-7606T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526887 | ||||||
| chr9:105526996
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-7497A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105526996 | ||||||
| chr9:105527072
|
T | C | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1026-7421T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527072 | ||||||
| chr9:105527261
|
C | A | 3 | a0001c0001t0004g0112a0001c0001t0004g0115a0001c0001t0004g0131 | 3 | HG00099.hp1 HG01517.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1026-7232C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527261 | ||||||
| chr9:105527297
|
T | G | 2 | a0001c0001t0005g0150a0001c0001t0030g0152 | 2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1026-7196T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527297 | ||||||
| chr9:105527560
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6933T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527560 | ||||||
| chr9:105527574
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6919G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527574 | ||||||
| chr9:105527598
|
C | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6895C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527598 | ||||||
| chr9:105527621
|
T | TATC | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6869_1026-686 others(7): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105527621 | |||||
| chr9:105527705
|
C | CA | 34 | a0001c0001t0005g0146a0001c0001t0005g0156a0001c0001t0005g0157others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1026-6776dupA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105527705 | |||||
| chr9:105527768
|
C | T | 44 | a0001c0001t0004g0001a0001c0001t0004g0106a0001c0001t0004g0107others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1026-6725C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527768 | ||||||
| chr9:105527828
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6665T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527828 | ||||||
| chr9:105527979
|
C | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6514C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105527979 | ||||||
| chr9:105528014
|
G | A | 38 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1026-6479G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528014 | ||||||
| chr9:105528156
|
G | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6337G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528156 | ||||||
| chr9:105528222
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1026-6271A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528222 | ||||||
| chr9:105528237
|
C | T | 13 | a0001c0001t0005g0179a0001c0001t0005g0180a0001c0001t0005g0181others(10): Show | 13 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1026-6256C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528237 | ||||||
| chr9:105528293
|
T | G | 5 | a0001c0001t0040g0223a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-6200T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528293 | ||||||
| chr9:105528310
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6183C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528310 | ||||||
| chr9:105528311
|
G | A | 1 | a0001c0001t0004g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-6182G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528311 | ||||||
| chr9:105528313
|
C | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6180C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528313 | ||||||
| chr9:105528314
|
C | T | 49 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(46): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1026-6179C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528314 | ||||||
| chr9:105528326
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-6167A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528326 | ||||||
| chr9:105528426
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-6067A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528426 | ||||||
| chr9:105528526
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-5967A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528526 | ||||||
| chr9:105528562
|
G | A | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1026-5931G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528562 | ||||||
| chr9:105528592
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-5901A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528592 | ||||||
| chr9:105528702
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1026-5791A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528702 | ||||||
| chr9:105528953
|
G | A | 1 | a0001c0001t0005g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1026-5540G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528953 | ||||||
| chr9:105528956
|
A | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1026-5537A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105528956 | ||||||
| chr9:105529013
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-5480A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529013 | ||||||
| chr9:105529080
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1026-5413C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529080 | ||||||
| chr9:105529093
|
G | T | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1026-5400G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529093 | ||||||
| chr9:105529164
|
G | C | 2 | a0001c0001t0011g0312a0001c0001t0011g0313 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1026-5329G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529164 | ||||||
| chr9:105529299
|
C | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-5194C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529299 | ||||||
| chr9:105529418
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1026-5075A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529418 | ||||||
| chr9:105529440
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18966.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1026-5053G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529440 | ||||||
| chr9:105529588
|
CAG | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4900_1026-489 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105529588 | |||||
| chr9:105529748
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4745C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529748 | ||||||
| chr9:105529783
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4710A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529783 | ||||||
| chr9:105529993
|
A | C | 2 | a0001c0001t0003g0323a0001c0001t0003g0335 | 2 | NA19004.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1026-4500A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105529993 | ||||||
| chr9:105530057
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1026-4436A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530057 | ||||||
| chr9:105530096
|
G | A | 1 | a0001c0001t0006g0086 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1026-4397G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530096 | ||||||
| chr9:105530149
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4344A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530149 | ||||||
| chr9:105530201
|
T | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1026-4292T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530201 | ||||||
| chr9:105530220
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4273G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530220 | ||||||
| chr9:105530245
|
G | C | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-4248G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530245 | ||||||
| chr9:105530273
|
T | C | 227 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(224): Show | 229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1026-4220T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530273 | ||||||
| chr9:105530298
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1026-4195G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530298 | ||||||
| chr9:105530342
|
T | C | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | NA18973.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1026-4151T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530342 | ||||||
| chr9:105530409
|
CCTTA | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4079_1026-407 others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105530409 | |||||
| chr9:105530414
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-4079C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530414 | ||||||
| chr9:105530501
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0043g0269 | 2 | HG00438.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1026-3992T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530501 | ||||||
| chr9:105530603
|
C | T | 23 | a0001c0001t0003g0324a0001c0001t0003g0336a0001c0001t0003g0337others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-3890C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530603 | ||||||
| chr9:105530693
|
G | A | 5 | a0001c0001t0040g0223a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-3800G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530693 | ||||||
| chr9:105530761
|
G | A | 77 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(74): Show | 78 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1026-3732G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530761 | ||||||
| chr9:105530816
|
G | A | 5 | a0001c0001t0040g0223a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-3677G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530816 | ||||||
| chr9:105530856
|
A | C | 1 | a0001c0001t0004g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1026-3637A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530856 | ||||||
| chr9:105530859
|
A | G | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026-3634A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530859 | ||||||
| chr9:105530869
|
C | CTATT | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-3622_1026-362 others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105530869 | |||||
| chr9:105530894
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1026-3599A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530894 | ||||||
| chr9:105530942
|
T | A | 212 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(209): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1026-3551T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105530942 | ||||||
| chr9:105531003
|
T | C | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1026-3490T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531003 | ||||||
| chr9:105531035
|
G | A | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026-3458G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531035 | ||||||
| chr9:105531156
|
T | C | 7 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-3337T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531156 | ||||||
| chr9:105531172
|
G | A | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-3321G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531172 | ||||||
| chr9:105531215
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-3278T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531215 | ||||||
| chr9:105531251
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-3242C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531251 | ||||||
| chr9:105531360
|
C | A | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-3133C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531360 | ||||||
| chr9:105531368
|
C | T | 1 | a0001c0001t0004g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1026-3125C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531368 | ||||||
| chr9:105531508
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-2985A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531508 | ||||||
| chr9:105531524
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1026-2969C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531524 | ||||||
| chr9:105531537
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-2956A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531537 | ||||||
| chr9:105531585
|
C | T | 1 | a0001c0002t0021g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1026-2908C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531585 | ||||||
| chr9:105531634
|
T | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-2859T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531634 | ||||||
| chr9:105531736
|
T | TAG | 227 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(224): Show | 229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1026-2757_1026-275 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531736 | ||||||
| chr9:105531866
|
G | A | 4 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-2627G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531866 | ||||||
| chr9:105531905
|
G | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-2588G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531905 | ||||||
| chr9:105531972
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-2521G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105531972 | ||||||
| chr9:105532057
|
G | A | 1 | a0001c0002t0021g0317 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1026-2436G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532057 | ||||||
| chr9:105532169
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-2324A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532169 | ||||||
| chr9:105532270
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(2): Show | 5 | NA18942.hp1 NA19001.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-2223C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532270 | ||||||
| chr9:105532327
|
T | C | 1 | a0001c0001t0015g0326 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1026-2166T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532327 | ||||||
| chr9:105532565
|
T | G | 1 | a0001c0001t0042g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026-1928T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532565 | ||||||
| chr9:105532595
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1026-1898C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532595 | ||||||
| chr9:105532664
|
A | G | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1829A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532664 | ||||||
| chr9:105532799
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1694G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532799 | ||||||
| chr9:105532887
|
A | T | 2 | a0001c0001t0003g0370a0001c0001t0003g0371 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1026-1606A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532887 | ||||||
| chr9:105532894
|
T | G | 1 | a0001c0001t0004g0114 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1026-1599T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532894 | ||||||
| chr9:105532942
|
G | A | 265 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(262): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1026-1551G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105532942 | ||||||
| chr9:105533023
|
T | C | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1026-1470T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533023 | ||||||
| chr9:105533026
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1467G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533026 | ||||||
| chr9:105533157
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-1336T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533157 | ||||||
| chr9:105533416
|
C | CTT | 14 | a0001c0001t0001g0218a0001c0001t0002g0027a0001c0001t0002g0083others(11): Show | 14 | HG00597.hp1 HG01074.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026-1054_1026-105 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTT | 8 | a0001c0001t0002g0061a0001c0001t0004g0132a0001c0001t0004g0203others(5): Show | 8 | HG00140.hp2 HG01243.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1055_1026-105 others(7): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTT | 6 | a0001c0001t0005g0146a0001c0001t0005g0161a0001c0001t0005g0166others(3): Show | 6 | HG01167.hp1 HG01515.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1058_1026-105 others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0010a0001c0001t0003g0324a0001c0001t0005g0150others(3): Show | 6 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1061_1026-105 others(13): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(3): Show |
27 | a0001c0001t0003g0005a0001c0001t0003g0320a0001c0001t0003g0321others(24): Show | 28 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1026-1062_1026-105 others(14): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(4): Show |
21 | a0001c0001t0003g0236a0001c0001t0003g0331a0001c0001t0003g0336others(18): Show | 21 | HG00323.hp1 HG01167.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.1026-1063_1026-105 others(15): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(5): Show |
13 | a0001c0001t0001g0270a0001c0001t0003g0318a0001c0001t0003g0322others(10): Show | 13 | HG01975.hp2 HG02027.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1026-1064_1026-105 others(16): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(6): Show |
23 | a0001c0001t0001g0085a0001c0001t0001g0210a0001c0001t0001g0212others(20): Show | 23 | HG00673.hp1 HG01081.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-1065_1026-105 others(17): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(7): Show |
56 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0205others(53): Show | 57 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1026-1066_1026-105 others(18): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(8): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0208a0001c0001t0001g0221others(25): Show | 29 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1026-1067_1026-105 others(19): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(9): Show |
13 | a0001c0001t0001g0261a0001c0001t0001g0267a0001c0001t0001g0285others(10): Show | 13 | HG01106.hp1 HG01261.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1026-1068_1026-105 others(20): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(10): Show |
28 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0018others(25): Show | 28 | HG00323.hp2 HG01069.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1026-1069_1026-105 others(21): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(11): Show |
20 | a0001c0001t0001g0243a0001c0001t0002g0017a0001c0001t0002g0023others(17): Show | 20 | HG01109.hp1 HG01993.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1026-1070_1026-105 others(22): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(12): Show |
23 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0013others(20): Show | 23 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026-1071_1026-105 others(23): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0222a0001c0001t0002g0047a0001c0001t0004g0142others(3): Show | 6 | HG01109.hp2 HG01358.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1072_1026-105 others(24): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(14): Show |
6 | a0001c0001t0002g0035a0001c0001t0002g0056a0001c0001t0002g0079others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1073_1026-105 others(25): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(15): Show |
8 | a0001c0001t0002g0038a0001c0001t0002g0050a0001c0001t0002g0059others(5): Show | 8 | HG00558.hp1 HG02074.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-1074_1026-105 others(26): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(16): Show |
8 | a0001c0001t0002g0037a0001c0001t0004g0109a0001c0001t0004g0114others(5): Show | 8 | HG00639.hp2 HG01361.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1075_1026-105 others(27): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(17): Show |
8 | a0001c0001t0002g0020a0001c0001t0002g0071a0001c0001t0004g0131others(5): Show | 8 | HG01891.hp2 HG01943.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-1076_1026-105 others(28): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(18): Show |
6 | a0001c0001t0002g0029a0001c0001t0002g0057a0001c0001t0004g0112others(3): Show | 6 | HG00735.hp2 HG01192.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(29): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0007g0195 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(30): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG00741.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(31): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(21): Show |
2 | a0001c0001t0005g0177a0001c0001t0007g0202 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(32): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0004g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(33): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0005g0157a0001c0001t0005g0176 | 2 | HG02630.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(34): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0004g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(35): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(25): Show |
3 | a0001c0001t0002g0009a0001c0001t0004g0115a0001c0001t0005g0174 | 3 | HG00099.hp1 HG03654.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(36): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0005g0168a0001c0001t0005g0169 | 2 | HG00140.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(37): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0004g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(38): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0005g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(39): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(33): Show |
2 | a0001c0001t0005g0171a0001c0001t0005g0172 | 2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1026-1053_1026-105 others(44): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533416
|
C | CTTTTTTT others(35): Show |
1 | a0001c0001t0005g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1026-1053_1026-105 others(46): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533416 | |||||
| chr9:105533483
|
C | T | 5 | a0001c0001t0040g0223a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-1010C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533483 | ||||||
| chr9:105533601
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1026-892T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533601 | ||||||
| chr9:105533619
|
C | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-874C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533619 | ||||||
| chr9:105533656
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1026-837C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533656 | ||||||
| chr9:105533662
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0280 | 2 | HG00621.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1026-831C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533662 | ||||||
| chr9:105533663
|
C | T | 1 | a0001c0001t0009g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1026-830C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533663 | ||||||
| chr9:105533664
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1026-829G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533664 | ||||||
| chr9:105533718
|
GC | G | 280 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(277): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1026-768delC | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr9 | 105533718 | |||||
| chr9:105533741
|
A | T | 1 | a0001c0001t0004g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1026-752A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533741 | ||||||
| chr9:105533777
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-716C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533777 | ||||||
| chr9:105533848
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1026-645C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533848 | ||||||
| chr9:105533919
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-574C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105533919 | ||||||
| chr9:105534059
|
C | T | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1026-434C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534059 | ||||||
| chr9:105534138
|
C | T | 4 | a0001c0001t0015g0326a0001c0001t0015g0327a0001c0001t0015g0328others(1): Show | 4 | NA18973.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-355C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534138 | ||||||
| chr9:105534232
|
C | T | 5 | a0001c0001t0004g0143a0001c0001t0011g0312a0001c0001t0011g0313others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-261C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534232 | ||||||
| chr9:105534296
|
T | C | 49 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(46): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1026-197T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534296 | ||||||
| chr9:105534381
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-112A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534381 | ||||||
| chr9:105534457
|
A | C | 1 | a0001c0001t0002g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1026-36A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 10/13 | chr9 | 105534457 | ||||||
| chr9:105534606
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+13A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/13 | chr9 | 105534606 | ||||||
| chr9:105534634
|
A | G | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1126+41A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/13 | chr9 | 105534634 | ||||||
| chr9:105534650
|
C | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1126+57C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/13 | chr9 | 105534650 | ||||||
| chr9:105534987
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127-80T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/13 | chr9 | 105534987 | ||||||
| chr9:105534993
|
G | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1127-74G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 11/13 | chr9 | 105534993 | ||||||
| chr9:105535459
|
T | C | 5 | a0001c0001t0040g0223a0001c0002t0010g0105a0001c0002t0010g0110others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+141T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535459 | ||||||
| chr9:105535501
|
C | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+183C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535501 | ||||||
| chr9:105535767
|
C | T | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378+449C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535767 | ||||||
| chr9:105535815
|
G | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+497G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535815 | ||||||
| chr9:105535847
|
A | G | 1 | a0001c0001t0003g0366 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1378+529A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535847 | ||||||
| chr9:105535902
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1378+584G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105535902 | ||||||
| chr9:105536318
|
T | C | 4 | a0001c0001t0019g0258a0001c0001t0019g0294a0001c0002t0021g0316others(1): Show | 4 | HG03098.hp2 HG03130.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+1000T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536318 | ||||||
| chr9:105536319
|
C | T | 1 | a0001c0001t0005g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1378+1001C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536319 | ||||||
| chr9:105536323
|
C | T | 1 | a0001c0001t0007g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1378+1005C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536323 | ||||||
| chr9:105536573
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1255C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536573 | ||||||
| chr9:105536624
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1306G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536624 | ||||||
| chr9:105536700
|
G | A | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1378+1382G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536700 | ||||||
| chr9:105536738
|
C | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+1420C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536738 | ||||||
| chr9:105536763
|
GT | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378+1447delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 105536763 | |||||
| chr9:105536809
|
G | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+1491G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536809 | ||||||
| chr9:105536909
|
T | G | 48 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(45): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1378+1591T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536909 | ||||||
| chr9:105536915
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1597C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536915 | ||||||
| chr9:105536972
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1654G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105536972 | ||||||
| chr9:105537043
|
G | A | 1 | a0001c0001t0003g0318 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1378+1725G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537043 | ||||||
| chr9:105537134
|
A | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1378+1816A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537134 | ||||||
| chr9:105537139
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1378+1821C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537139 | ||||||
| chr9:105537164
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1378+1846A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537164 | ||||||
| chr9:105537272
|
C | T | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1378+1954C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537272 | ||||||
| chr9:105537273
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1378+1955G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537273 | ||||||
| chr9:105537282
|
CAGTTA | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+1966_1378+197 others(9): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr9 | 105537282 | |||||
| chr9:105537297
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1379-1966A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537297 | ||||||
| chr9:105537449
|
C | G | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1379-1814C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537449 | ||||||
| chr9:105537548
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-1715G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537548 | ||||||
| chr9:105537550
|
A | G | 1 | a0001c0002t0010g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1379-1713A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537550 | ||||||
| chr9:105537580
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-1683G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537580 | ||||||
| chr9:105537716
|
A | G | 10 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1379-1547A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537716 | ||||||
| chr9:105537801
|
A | T | 1 | a0001c0001t0007g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1379-1462A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537801 | ||||||
| chr9:105537905
|
G | A | 9 | a0001c0001t0005g0179a0001c0001t0005g0180a0001c0001t0005g0181others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-1358G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105537905 | ||||||
| chr9:105538062
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-1201G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538062 | ||||||
| chr9:105538454
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1379-809A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538454 | ||||||
| chr9:105538468
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-795T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538468 | ||||||
| chr9:105538597
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02040.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1379-666T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538597 | ||||||
| chr9:105538687
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-576A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538687 | ||||||
| chr9:105538764
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1379-499C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538764 | ||||||
| chr9:105538765
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0014g0206a0001c0001t0014g0207others(2): Show | 5 | HG01109.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-498G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538765 | ||||||
| chr9:105538904
|
C | T | 1 | a0001c0001t0005g0164 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1379-359C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538904 | ||||||
| chr9:105538956
|
A | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1379-307A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538956 | ||||||
| chr9:105538977
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1379-286G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105538977 | ||||||
| chr9:105539026
|
C | A | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1379-237C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105539026 | ||||||
| chr9:105539026
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1379-237C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105539026 | ||||||
| chr9:105539133
|
TAATC | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-129_1379-126d others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105539133 | ||||||
| chr9:105539196
|
C | T | 1 | a0001c0001t0010g0108 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1379-67C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105539196 | ||||||
| chr9:105539227
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1379-36G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 12/13 | chr9 | 105539227 | ||||||
| chr9:105539369
|
C | T | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1467+18C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105539369 | ||||||
| chr9:105539401
|
G | A | 4 | a0001c0001t0005g0150a0001c0001t0005g0151a0001c0001t0005g0153others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+50G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105539401 | ||||||
| chr9:105539498
|
C | T | 11 | a0001c0001t0005g0158a0001c0001t0005g0178a0001c0001t0005g0179others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1467+147C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105539498 | ||||||
| chr9:105539619
|
G | C | 1 | a0001c0001t0023g0319 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1467+268G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105539619 | ||||||
| chr9:105539626
|
GA | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+277delA | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105539626 | |||||
| chr9:105539635
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1467+284G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105539635 | ||||||
| chr9:105540046
|
C | T | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1467+695C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540046 | ||||||
| chr9:105540422
|
G | C | 2 | a0001c0001t0004g0148a0001c0001t0042g0147 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1467+1071G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540422 | ||||||
| chr9:105540613
|
G | A | 2 | a0001c0001t0003g0354a0001c0001t0003g0355 | 2 | NA18962.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1467+1262G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540613 | ||||||
| chr9:105540753
|
A | G | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467+1402A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540753 | ||||||
| chr9:105540919
|
T | G | 1 | a0001c0001t0002g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1467+1568T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540919 | ||||||
| chr9:105540934
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+1583A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105540934 | ||||||
| chr9:105541062
|
T | C | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1467+1711T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105541062 | ||||||
| chr9:105541253
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0239a0001c0001t0001g0247others(1): Show | 5 | NA18969.hp1 NA18982.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+1902A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105541253 | ||||||
| chr9:105541266
|
AAGGG | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+1920_1467+192 others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105541266 | |||||
| chr9:105541288
|
CT | C | 122 | a0001c0001t0001g0284a0001c0001t0002g0007a0001c0001t0002g0021others(119): Show | 124 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1467+1953delT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105541288 | |||||
| chr9:105541288
|
CTT | C | 8 | a0001c0001t0003g0351a0001c0001t0003g0371a0001c0001t0004g0112others(5): Show | 8 | HG01069.hp2 HG01517.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1467+1952_1467+195 others(6): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105541288 | |||||
| chr9:105541344
|
T | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+1993T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105541344 | ||||||
| chr9:105541512
|
CTAATTA | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+2164_1467+216 others(10): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105541512 | |||||
| chr9:105541859
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1467+2508G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105541859 | ||||||
| chr9:105541984
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+2633A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105541984 | ||||||
| chr9:105542076
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1467+2725A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542076 | ||||||
| chr9:105542219
|
C | A | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1467+2868C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542219 | ||||||
| chr9:105542222
|
A | G | 1 | a0003c0005t0034g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1467+2871A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542222 | ||||||
| chr9:105542480
|
G | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+3129G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542480 | ||||||
| chr9:105542726
|
G | A | 61 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1467+3375G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542726 | ||||||
| chr9:105542754
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0280 | 2 | HG00621.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1467+3403T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542754 | ||||||
| chr9:105542787
|
T | A | 1 | a0001c0001t0002g0008 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1467+3436T>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542787 | ||||||
| chr9:105542903
|
G | A | 264 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1468-3455G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542903 | ||||||
| chr9:105542917
|
C | G | 1 | a0001c0001t0006g0341 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1468-3441C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542917 | ||||||
| chr9:105542985
|
T | G | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG00280.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1468-3373T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105542985 | ||||||
| chr9:105543102
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1468-3256A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543102 | ||||||
| chr9:105543296
|
T | C | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1468-3062T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543296 | ||||||
| chr9:105543300
|
C | T | 4 | a0001c0001t0013g0094a0001c0001t0013g0095a0001c0001t0013g0096others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-3058C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543300 | ||||||
| chr9:105543357
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-3001T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543357 | ||||||
| chr9:105543405
|
A | C | 62 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0318others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1468-2953A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543405 | ||||||
| chr9:105543406
|
C | T | 1 | a0001c0001t0011g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1468-2952C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543406 | ||||||
| chr9:105543473
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2885G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543473 | ||||||
| chr9:105543478
|
C | T | 101 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1468-2880C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543478 | ||||||
| chr9:105543501
|
G | C | 49 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(46): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1468-2857G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543501 | ||||||
| chr9:105543530
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2828C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543530 | ||||||
| chr9:105543597
|
C | A | 1 | a0001c0001t0023g0339 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1468-2761C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543597 | ||||||
| chr9:105543701
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2657C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543701 | ||||||
| chr9:105543728
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1468-2630C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543728 | ||||||
| chr9:105543810
|
A | AT | 5 | a0001c0001t0001g0002a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 6 | NA18962.hp2 NA18972.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-2544dupT | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105543810 | |||||
| chr9:105543857
|
A | C | 1 | a0002c0004t0029g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1468-2501A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543857 | ||||||
| chr9:105543870
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2488G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543870 | ||||||
| chr9:105543943
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-2415C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105543943 | ||||||
| chr9:105544014
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0215 | 3 | HG01081.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1468-2344T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544014 | ||||||
| chr9:105544118
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1468-2240C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544118 | ||||||
| chr9:105544409
|
A | G | 10 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468-1949A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544409 | ||||||
| chr9:105544486
|
C | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1872C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544486 | ||||||
| chr9:105544567
|
A | G | 4 | a0001c0001t0015g0326a0001c0001t0015g0327a0001c0001t0015g0328others(1): Show | 4 | NA18973.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-1791A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544567 | ||||||
| chr9:105544594
|
A | G | 4 | a0001c0001t0015g0326a0001c0001t0015g0327a0001c0001t0015g0328others(1): Show | 4 | NA18973.hp2 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-1764A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544594 | ||||||
| chr9:105544672
|
G | T | 1 | a0001c0001t0040g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-1686G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544672 | ||||||
| chr9:105544698
|
T | C | 2 | a0001c0001t0003g0372a0001c0001t0003g0373 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1468-1660T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544698 | ||||||
| chr9:105544740
|
T | C | 263 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0002g0006others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1468-1618T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544740 | ||||||
| chr9:105544741
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1468-1617G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544741 | ||||||
| chr9:105544784
|
A | G | 2 | a0001c0002t0021g0316a0001c0002t0021g0317 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1468-1574A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544784 | ||||||
| chr9:105544823
|
C | A | 5 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(2): Show | 5 | HG02723.hp2 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468-1535C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544823 | ||||||
| chr9:105544830
|
C | T | 1 | a0001c0001t0015g0327 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1468-1528C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544830 | ||||||
| chr9:105544922
|
T | G | 1 | a0001c0001t0003g0322 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1468-1436T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544922 | ||||||
| chr9:105544926
|
A | G | 1 | a0001c0002t0010g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1468-1432A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544926 | ||||||
| chr9:105544952
|
C | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1406C>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105544952 | ||||||
| chr9:105545154
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1204G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545154 | ||||||
| chr9:105545155
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1203T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545155 | ||||||
| chr9:105545166
|
G | A | 3 | a0001c0001t0004g0109a0001c0001t0004g0123a0001c0001t0004g0126 | 3 | HG00741.hp1 HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1468-1192G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545166 | ||||||
| chr9:105545213
|
A | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1145A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545213 | ||||||
| chr9:105545217
|
G | T | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1141G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545217 | ||||||
| chr9:105545227
|
T | TTGTC | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1128_1468-112 others(8): Show |
FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr9 | 105545227 | |||||
| chr9:105545232
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1126A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545232 | ||||||
| chr9:105545243
|
G | A | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1115G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545243 | ||||||
| chr9:105545262
|
C | T | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1096C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545262 | ||||||
| chr9:105545264
|
C | T | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1094C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545264 | ||||||
| chr9:105545265
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1093A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545265 | ||||||
| chr9:105545320
|
T | C | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-1038T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545320 | ||||||
| chr9:105545321
|
G | A | 4 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1037G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545321 | ||||||
| chr9:105545361
|
A | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-997A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545361 | ||||||
| chr9:105545418
|
T | C | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-940T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545418 | ||||||
| chr9:105545428
|
C | T | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-930C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545428 | ||||||
| chr9:105545430
|
G | A | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-928G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545430 | ||||||
| chr9:105545436
|
T | C | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-922T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545436 | ||||||
| chr9:105545439
|
G | A | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-919G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545439 | ||||||
| chr9:105545513
|
T | G | 39 | a0001c0001t0005g0146a0001c0001t0005g0150a0001c0001t0005g0151others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1468-845T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545513 | ||||||
| chr9:105545560
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-798T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545560 | ||||||
| chr9:105545568
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-790A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545568 | ||||||
| chr9:105545580
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-778T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545580 | ||||||
| chr9:105545588
|
G | A | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-770G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545588 | ||||||
| chr9:105545592
|
T | C | 7 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(4): Show | 7 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-766T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545592 | ||||||
| chr9:105545595
|
A | C | 7 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(4): Show | 7 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-763A>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545595 | ||||||
| chr9:105545598
|
G | A | 7 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(4): Show | 7 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-760G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545598 | ||||||
| chr9:105545616
|
G | C | 1 | a0001c0001t0002g0067 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1468-742G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545616 | ||||||
| chr9:105545637
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-721C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545637 | ||||||
| chr9:105545638
|
T | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-720T>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545638 | ||||||
| chr9:105545641
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-717C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545641 | ||||||
| chr9:105545650
|
G | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-708G>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545650 | ||||||
| chr9:105545651
|
T | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-707T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545651 | ||||||
| chr9:105545658
|
C | T | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-700C>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545658 | ||||||
| chr9:105545738
|
G | A | 7 | a0001c0001t0002g0055a0001c0001t0002g0073a0001c0001t0002g0077others(4): Show | 7 | NA18952.hp2 NA18961.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-620G>A | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105545738 | ||||||
| chr9:105546038
|
A | G | 14 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1468-320A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546038 | ||||||
| chr9:105546085
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-273A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546085 | ||||||
| chr9:105546160
|
A | T | 8 | a0001c0001t0012g0098a0001c0001t0012g0099a0001c0001t0012g0100others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1468-198A>T | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546160 | ||||||
| chr9:105546229
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1468-129T>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546229 | ||||||
| chr9:105546240
|
G | C | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-118G>C | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546240 | ||||||
| chr9:105546262
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1468-96C>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546262 | ||||||
| chr9:105546311
|
A | G | 4 | a0001c0001t0011g0312a0001c0001t0011g0313a0001c0001t0011g0314others(1): Show | 4 | HG02723.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-47A>G | FSD1L | ENSG00000106701.13 | transcript | ENST00000481272.6 | protein_coding | 13/13 | chr9 | 105546311 |