Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23131 |
|---|---|
| ensemblid | ENSG00000186566.13 |
| hgncid | 29066 |
| symbol | GPATCH8 |
| name | G-patch domain containing 8 |
| refseq_nuc | NM_001002909.4 |
| refseq_prot | NP_001002909.1 |
| ensembl_nuc | ENST00000591680.6 |
| ensembl_prot | ENSP00000467556.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44395281 |
| end | 44503406 |
| strand | - |
| ver | v1.2 |
| region | chr17:44395281-44503406 |
| region5000 | chr17:44390281-44508406 |
| regionname0 | GPATCH8_chr17_44395281_44503406 |
| regionname5000 | GPATCH8_chr17_44390281_44508406 |
| 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 | 1/0 | 1502 | 316 | 81 | 59 | 134 | 9 | 32 | 104 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0002 | 0/1 | 1502 | 3 | 0 | 0 | 0 | 1 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0003 | 0/0 | 1502 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0004 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0005 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0006 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0007 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0008 | 0/0 | 1502 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4509 | 155 | 45 | 22 | 67 | 4 | 16 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0002 | 0/0 | 4509 | 138 | 33 | 34 | 52 | 5 | 14 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0003 | 0/0 | 4509 | 12 | 0 | 2 | 9 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0004 | 0/0 | 4509 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0005 | 0/1 | 4509 | 3 | 0 | 0 | 0 | 1 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0006 | 0/0 | 4509 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0007 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0008 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0009 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0010 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0011 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0012 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0013 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0014 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0015 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| c0016 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2324 | 303 | 72 | 60 | 129 | 10 | 30 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0002 | 0/0 | 2324 | 7 | 7 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0003 | 0/0 | 2324 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0004 | 0/0 | 2324 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0005 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0006 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0007 | 0/0 | 2324 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0008 | 0/0 | 2324 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0009 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0010 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0011 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0012 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0013 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0014 | 0/0 | 2324 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0015 | 0/0 | 2324 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| t0016 | 0/0 | 2324 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4509 | 155 | 45 | 22 | 67 | 4 | 16 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002 | 0/0 | 4509 | 138 | 33 | 34 | 52 | 5 | 14 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0003 | 0/0 | 4509 | 12 | 0 | 2 | 9 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0004 | 0/0 | 4509 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0008 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0010 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0012 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0013 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0014 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0002c0005 | 0/1 | 4509 | 3 | 0 | 0 | 0 | 1 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0003c0006 | 0/0 | 4509 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0004c0015 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0005c0009 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0006c0011 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0007c0016 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0008c0007 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6832 | 148 | 43 | 21 | 65 | 4 | 14 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0003 | 0/0 | 6832 | 2 | 0 | 1 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0007 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0011 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0012 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0015 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0001t0016 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0001 | 0/0 | 6832 | 124 | 25 | 33 | 49 | 5 | 12 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0002 | 0/0 | 6832 | 7 | 7 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0004 | 0/0 | 6832 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0006 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0008 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0009 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0010 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0002t0014 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0003t0001 | 0/0 | 6832 | 12 | 0 | 2 | 9 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0004t0001 | 0/0 | 6832 | 6 | 0 | 0 | 6 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0008t0013 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0010t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0012t0001 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0013t0005 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0001c0014t0001 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0002c0005t0001 | 0/1 | 6832 | 3 | 0 | 0 | 0 | 1 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0003c0006t0001 | 0/0 | 6832 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0004c0015t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0005c0009t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0006c0011t0001 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0007c0016t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| a0008c0007t0001 | 0/0 | 6832 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | copy fasta | chr17 | 44390281 | 44508406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0015g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0008g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0002t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0008t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0010t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0012t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0013t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0001c0014t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0002c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0002c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0002c0005t0001g0054 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0003c0006t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0003c0006t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0004c0015t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0005c0009t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0006c0011t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0007c0016t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| a0008c0007t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0005 | t0001 | g0034 | EUR | GBR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0262 | EUR | GBR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0168 | EUR | FIN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01069 | hp1 | a0001 | c0002 | t0008 | g0258 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01109 | hp2 | a0008 | c0007 | t0001 | g0163 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0321 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0312 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01261 | hp1 | a0003 | c0006 | t0001 | g0242 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0319 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01496 | hp1 | a0003 | c0006 | t0001 | g0239 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01978 | hp1 | a0001 | c0014 | t0001 | g0053 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0023 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | CDX | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0299 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02451 | hp2 | a0004 | c0015 | t0001 | g0200 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02523 | hp2 | a0001 | c0002 | t0009 | g0278 | EAS | KHV | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0317 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02922 | hp1 | a0005 | c0009 | t0001 | g0143 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0127 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0096 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03139 | hp2 | a0001 | c0010 | t0001 | g0134 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03195 | hp1 | a0001 | c0008 | t0013 | g0164 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03239 | hp1 | a0001 | c0001 | t0015 | g0141 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03453 | hp1 | a0001 | c0013 | t0005 | g0325 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03490 | hp1 | a0002 | c0005 | t0001 | g0035 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0274 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0273 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03540 | hp1 | a0007 | c0016 | t0001 | g0122 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03654 | hp1 | a0001 | c0012 | t0001 | g0297 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0179 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0253 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04199 | hp2 | a0006 | c0011 | t0001 | g0201 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | STU | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | YRI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | YRI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | CHB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | CHB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | YRI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18967 | hp1 | a0001 | c0004 | t0001 | g0219 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18967 | hp2 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18972 | hp1 | a0001 | c0002 | t0010 | g0217 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19003 | hp1 | a0001 | c0002 | t0014 | g0254 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0303 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0272 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0238 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | ASW | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0275 | EUR | TSI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0156 | EUR | TSI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0251 | EUR | TSI | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | GIH | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | USA | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | USA | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | USA | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0001 | g0054 | REF | REF | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | GPATCH8_chr17_44390281_44508406 | GPATCH8 | chr17 | 44390281 | 44508406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44398501
|
C | G | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.3576G>C | p.Gln1192His | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 3612/6832 | 3576/4509 | 1192/1502 | chr17 | 44398501 | ||
| chr17:44398594
|
A | C | 1 | a0002 | 3 | HG00099.hp1 HG03490.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.3483T>G | p.Cys1161Trp | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 3519/6832 | 3483/4509 | 1161/1502 | chr17 | 44398594 | ||
| chr17:44399486
|
C | T | 1 | a0003 | 2 | HG01261.hp1 HG01496.hp1 |
missense_variant | MODERATE | c.2591G>A | p.Arg864His | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2627/6832 | 2591/4509 | 864/1502 | chr17 | 44399486 | ||
| chr17:44399519
|
C | T | 1 | a0005 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2558G>A | p.Arg853His | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2594/6832 | 2558/4509 | 853/1502 | chr17 | 44399519 | ||
| chr17:44401138
|
T | A | 1 | a0004 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.939A>T | p.Glu313Asp | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 975/6832 | 939/4509 | 313/1502 | chr17 | 44401138 | ||
| chr17:44401253
|
G | A | 1 | a0007 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.824C>T | p.Ala275Val | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 860/6832 | 824/4509 | 275/1502 | chr17 | 44401253 | ||
| chr17:44401266
|
C | T | 1 | a0008 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.811G>A | p.Gly271Arg | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 847/6832 | 811/4509 | 271/1502 | chr17 | 44401266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44398189
|
C | T | 1 | a0001c0012 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.3888G>A | p.Gly1296Gly | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 3924/6832 | 3888/4509 | 1296/1502 | chr17 | 44398189 | ||
| chr17:44398615
|
G | C | 8 | a0001c0002a0001c0003a0001c0004others(5): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
synonymous_variant | LOW | c.3462C>G | p.Thr1154Thr | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 3498/6832 | 3462/4509 | 1154/1502 | chr17 | 44398615 | ||
| chr17:44399041
|
G | A | 1 | a0001c0003 | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
synonymous_variant | LOW | c.3036C>T | p.His1012His | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 3072/6832 | 3036/4509 | 1012/1502 | chr17 | 44399041 | ||
| chr17:44399119
|
C | G | 1 | a0001c0010 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.2958G>C | p.Arg986Arg | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2994/6832 | 2958/4509 | 986/1502 | chr17 | 44399119 | ||
| chr17:44399584
|
C | T | 1 | a0001c0008 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2493G>A | p.Lys831Lys | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2529/6832 | 2493/4509 | 831/1502 | chr17 | 44399584 | ||
| chr17:44399821
|
A | G | 1 | a0001c0004 | 6 | HG00423.hp1 NA18950.hp2 NA18967.hp1 others(3): Show |
synonymous_variant | LOW | c.2256T>C | p.Asp752Asp | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2292/6832 | 2256/4509 | 752/1502 | chr17 | 44399821 | ||
| chr17:44399914
|
T | C | 1 | a0001c0013 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2163A>G | p.Ser721Ser | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 2199/6832 | 2163/4509 | 721/1502 | chr17 | 44399914 | ||
| chr17:44400415
|
T | C | 1 | a0001c0014 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.1662A>G | p.Glu554Glu | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1698/6832 | 1662/4509 | 554/1502 | chr17 | 44400415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44395824
|
C | T | 1 | a0001c0001t0012 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1744 | chr17 | 44395824 | |||||
| chr17:44395858
|
T | C | 1 | a0001c0008t0013 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1710 | chr17 | 44395858 | |||||
| chr17:44396147
|
T | C | 1 | a0001c0002t0014 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1421 | chr17 | 44396147 | |||||
| chr17:44396242
|
G | C | 1 | a0001c0002t0004 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1326C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1326 | chr17 | 44396242 | |||||
| chr17:44396374
|
C | T | 1 | a0001c0001t0011 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1194 | chr17 | 44396374 | |||||
| chr17:44396466
|
G | A | 1 | a0001c0001t0015 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1102C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 1102 | chr17 | 44396466 | |||||
| chr17:44396604
|
T | C | 1 | a0001c0001t0016 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 964 | chr17 | 44396604 | |||||
| chr17:44396616
|
A | T | 1 | a0001c0002t0010 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 952 | chr17 | 44396616 | |||||
| chr17:44396627
|
C | T | 1 | a0001c0001t0003 | 2 | HG00738.hp2 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*941G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 941 | chr17 | 44396627 | |||||
| chr17:44396651
|
C | T | 1 | a0001c0002t0009 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 917 | chr17 | 44396651 | |||||
| chr17:44396712
|
C | T | 1 | a0001c0002t0008 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 856 | chr17 | 44396712 | |||||
| chr17:44397004
|
A | G | 1 | a0001c0001t0007 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 564 | chr17 | 44397004 | |||||
| chr17:44397244
|
G | A | 1 | a0001c0002t0002 | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*324C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 324 | chr17 | 44397244 | |||||
| chr17:44397301
|
G | T | 1 | a0001c0002t0006 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*267C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 267 | chr17 | 44397301 | |||||
| chr17:44397537
|
C | T | 1 | a0001c0013t0005 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 8/8 | 31 | chr17 | 44397537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44401615
|
G | A | 2 | a0001c0002t0001g0227a0001c0002t0001g0243 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.624-162C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44401615 | ||||||
| chr17:44401903
|
C | T | 6 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0091others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-450G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44401903 | ||||||
| chr17:44401926
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18959.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.624-473G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44401926 | ||||||
| chr17:44401970
|
C | T | 1 | a0001c0002t0001g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.624-517G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44401970 | ||||||
| chr17:44402022
|
AAT | A | 12 | a0001c0002t0001g0198a0001c0002t0001g0235a0001c0002t0001g0243others(9): Show | 12 | HG01069.hp1 HG01169.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.624-571_624-570del others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402022 | ||||||
| chr17:44402023
|
AT | A | 132 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0202others(129): Show | 132 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.624-571delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402023 | ||||||
| chr17:44402024
|
T | A | 19 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(16): Show | 19 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.624-571A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402024 | ||||||
| chr17:44402028
|
A | T | 2 | a0001c0002t0001g0012a0001c0002t0001g0014 | 2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.624-575T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402028 | ||||||
| chr17:44402060
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG00423.hp2 NA18612.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.624-607C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402060 | ||||||
| chr17:44402164
|
A | T | 1 | a0001c0002t0001g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.624-711T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402164 | ||||||
| chr17:44402218
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.624-765C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402218 | ||||||
| chr17:44402324
|
C | CA | 42 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0043others(39): Show | 42 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.624-872dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402324 | ||||||
| chr17:44402324
|
CA | C | 8 | a0001c0001t0001g0104a0001c0002t0001g0011a0001c0002t0001g0017others(5): Show | 8 | HG01074.hp1 HG01109.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.624-872delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402324 | ||||||
| chr17:44402557
|
G | C | 1 | a0002c0005t0001g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.624-1104C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402557 | ||||||
| chr17:44402674
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.624-1221A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402674 | ||||||
| chr17:44402945
|
G | A | 15 | a0001c0001t0001g0037a0001c0001t0001g0183a0001c0001t0001g0184others(12): Show | 15 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.624-1492C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402945 | ||||||
| chr17:44402987
|
T | C | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.624-1534A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44402987 | ||||||
| chr17:44403169
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.624-1716C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403169 | ||||||
| chr17:44403227
|
C | T | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.624-1774G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403227 | ||||||
| chr17:44403418
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.624-1965A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403418 | ||||||
| chr17:44403433
|
G | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.624-1980C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403433 | ||||||
| chr17:44403652
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.624-2199T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403652 | ||||||
| chr17:44403691
|
CT | C | 155 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(152): Show | 155 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.623+2229delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403691 | ||||||
| chr17:44403691
|
CTT | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+2228_623+2229d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403691 | ||||||
| chr17:44403715
|
T | C | 323 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.623+2206A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403715 | ||||||
| chr17:44403716
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.623+2205C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403716 | ||||||
| chr17:44403828
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.623+2093C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403828 | ||||||
| chr17:44403835
|
A | G | 7 | a0001c0002t0001g0271a0001c0002t0001g0291a0001c0002t0001g0298others(4): Show | 7 | HG01169.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+2086T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403835 | ||||||
| chr17:44403974
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+1947C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403974 | ||||||
| chr17:44403989
|
C | T | 4 | a0001c0002t0001g0205a0001c0002t0001g0235a0001c0002t0001g0240others(1): Show | 4 | HG02735.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.623+1932G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44403989 | ||||||
| chr17:44404125
|
C | G | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.623+1796G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44404125 | ||||||
| chr17:44404273
|
G | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+1648C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44404273 | ||||||
| chr17:44404867
|
A | G | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+1054T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44404867 | ||||||
| chr17:44404923
|
G | A | 121 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.623+998C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44404923 | ||||||
| chr17:44404932
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.623+989C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44404932 | ||||||
| chr17:44405009
|
C | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.623+912G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405009 | ||||||
| chr17:44405047
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.623+874G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405047 | ||||||
| chr17:44405057
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.623+864A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405057 | ||||||
| chr17:44405209
|
C | CT | 7 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0188others(4): Show | 7 | HG00438.hp1 HG00438.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.623+711dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405209 | ||||||
| chr17:44405209
|
CT | C | 29 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.623+711delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405209 | ||||||
| chr17:44405255
|
A | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.623+666T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405255 | ||||||
| chr17:44405365
|
C | T | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.623+556G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405365 | ||||||
| chr17:44405514
|
GT | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.623+406delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405514 | ||||||
| chr17:44405544
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.623+377C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405544 | ||||||
| chr17:44405559
|
C | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.623+362G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405559 | ||||||
| chr17:44405755
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.623+166G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405755 | ||||||
| chr17:44405768
|
T | A | 1 | a0001c0002t0001g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.623+153A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405768 | ||||||
| chr17:44405795
|
C | T | 17 | a0001c0002t0001g0208a0001c0002t0001g0210a0001c0002t0001g0211others(14): Show | 17 | HG00408.hp1 HG01261.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.623+126G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405795 | ||||||
| chr17:44405847
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0124 | 2 | NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.623+74T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405847 | ||||||
| chr17:44405865
|
T | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.623+56A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 7/7 | chr17 | 44405865 | ||||||
| chr17:44406163
|
T | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.493-112A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406163 | ||||||
| chr17:44406496
|
T | TG | 37 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0026others(34): Show | 38 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.493-446dupC | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406496 | ||||||
| chr17:44406496
|
T | TGG | 59 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0024others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.493-447_493-446dup others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406496 | ||||||
| chr17:44406496
|
T | TGGG | 47 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0036others(44): Show | 47 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.493-448_493-446dup others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406496 | ||||||
| chr17:44406496
|
T | TGGGG | 22 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(19): Show | 22 | HG00423.hp2 HG00741.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.493-449_493-446dup others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406496 | ||||||
| chr17:44406496
|
T | TGGGGGGG others(3): Show |
3 | a0001c0002t0001g0170a0001c0002t0001g0171a0001c0002t0001g0173 | 3 | HG01258.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.493-455_493-446dup others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406496 | ||||||
| chr17:44406506
|
G | GGGGGGT | 41 | a0001c0002t0001g0002a0001c0002t0001g0202a0001c0002t0001g0203others(38): Show | 41 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.493-456_493-455ins others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406506 | ||||||
| chr17:44406506
|
G | GGGGGT | 23 | a0001c0002t0001g0206a0001c0002t0001g0224a0001c0002t0001g0227others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.493-456_493-455ins others(5): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406506 | ||||||
| chr17:44406509
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-458A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406509 | ||||||
| chr17:44406554
|
A | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-503T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406554 | ||||||
| chr17:44406581
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-530T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406581 | ||||||
| chr17:44406598
|
A | G | 1 | a0002c0005t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.493-547T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406598 | ||||||
| chr17:44406616
|
C | G | 3 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300 | 3 | HG02258.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.493-565G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406616 | ||||||
| chr17:44406633
|
C | T | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.493-582G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406633 | ||||||
| chr17:44406738
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.493-687G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406738 | ||||||
| chr17:44406751
|
G | C | 1 | a0001c0002t0001g0308 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.493-700C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406751 | ||||||
| chr17:44406951
|
C | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.493-900G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44406951 | ||||||
| chr17:44407143
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.493-1092A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407143 | ||||||
| chr17:44407160
|
T | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-1109A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407160 | ||||||
| chr17:44407545
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0100 | 3 | NA18612.hp1 NA18944.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.493-1494A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407545 | ||||||
| chr17:44407644
|
G | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG02074.hp2 HG02155.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-1593C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407644 | ||||||
| chr17:44407657
|
A | AT | 14 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0067others(11): Show | 14 | HG00642.hp2 HG01074.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.493-1607dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407657 | ||||||
| chr17:44407657
|
AT | A | 141 | a0001c0001t0001g0091a0001c0002t0001g0002a0001c0002t0001g0156others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.493-1607delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407657 | ||||||
| chr17:44407676
|
A | C | 125 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.493-1625T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407676 | ||||||
| chr17:44407796
|
A | G | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493-1745T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407796 | ||||||
| chr17:44407857
|
A | C | 6 | a0001c0002t0001g0198a0001c0002t0001g0216a0001c0002t0001g0251others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-1806T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44407857 | ||||||
| chr17:44408223
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0001g0291a0001c0002t0006g0272 | 3 | HG01169.hp1 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.493-2172C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44408223 | ||||||
| chr17:44408242
|
GGT | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.493-2193_493-2192d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44408242 | ||||||
| chr17:44408298
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0104 | 2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.493-2247C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44408298 | ||||||
| chr17:44408345
|
C | T | 8 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(5): Show | 8 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-2294G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44408345 | ||||||
| chr17:44409093
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.493-3042C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409093 | ||||||
| chr17:44409400
|
A | G | 5 | a0001c0002t0001g0319a0001c0002t0001g0320a0001c0002t0001g0321others(2): Show | 5 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-3349T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409400 | ||||||
| chr17:44409605
|
C | T | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.493-3554G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409605 | ||||||
| chr17:44409755
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.493-3704T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409755 | ||||||
| chr17:44409785
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.493-3734G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409785 | ||||||
| chr17:44409867
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-3816C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44409867 | ||||||
| chr17:44410191
|
G | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-4140C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410191 | ||||||
| chr17:44410229
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.493-4178C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410229 | ||||||
| chr17:44410269
|
T | A | 1 | a0001c0003t0001g0182 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.493-4218A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410269 | ||||||
| chr17:44410617
|
T | G | 12 | a0001c0003t0001g0144a0001c0003t0001g0166a0001c0003t0001g0174others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.493-4566A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410617 | ||||||
| chr17:44410787
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.493-4736T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410787 | ||||||
| chr17:44410853
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-4802A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410853 | ||||||
| chr17:44410957
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493-4906A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44410957 | ||||||
| chr17:44411221
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.493-5170G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411221 | ||||||
| chr17:44411295
|
C | A | 1 | a0001c0002t0001g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.493-5244G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411295 | ||||||
| chr17:44411658
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-5607A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411658 | ||||||
| chr17:44411682
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.493-5631C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411682 | ||||||
| chr17:44411806
|
T | C | 1 | a0001c0002t0001g0323 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.493-5755A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411806 | ||||||
| chr17:44411818
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.493-5767C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411818 | ||||||
| chr17:44411920
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.493-5869C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411920 | ||||||
| chr17:44411921
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.493-5870A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411921 | ||||||
| chr17:44411959
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.493-5908C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411959 | ||||||
| chr17:44411973
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.493-5922T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411973 | ||||||
| chr17:44411983
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.493-5932G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411983 | ||||||
| chr17:44411998
|
C | T | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.493-5947G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44411998 | ||||||
| chr17:44412000
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.493-5949C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412000 | ||||||
| chr17:44412153
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG00280.hp1 NA18941.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-6102G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412153 | ||||||
| chr17:44412218
|
C | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0104others(14): Show | 17 | HG00621.hp2 HG00738.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.493-6167G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412218 | ||||||
| chr17:44412229
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.493-6178T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412229 | ||||||
| chr17:44412291
|
G | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-6240C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412291 | ||||||
| chr17:44412418
|
C | T | 5 | a0001c0002t0001g0319a0001c0002t0001g0320a0001c0002t0001g0321others(2): Show | 5 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-6367G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412418 | ||||||
| chr17:44412425
|
C | T | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.493-6374G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412425 | ||||||
| chr17:44412727
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.493-6676G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412727 | ||||||
| chr17:44412801
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18941.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.493-6750T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44412801 | ||||||
| chr17:44413018
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.493-6967C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413018 | ||||||
| chr17:44413189
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-7138C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413189 | ||||||
| chr17:44413429
|
C | G | 1 | a0001c0012t0001g0297 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.493-7378G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413429 | ||||||
| chr17:44413544
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0102 | 3 | HG02300.hp2 HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.493-7493G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413544 | ||||||
| chr17:44413571
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.493-7520C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413571 | ||||||
| chr17:44413600
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7549A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413600 | ||||||
| chr17:44413601
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7550C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413601 | ||||||
| chr17:44413602
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7551T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413602 | ||||||
| chr17:44413604
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7553T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413604 | ||||||
| chr17:44413611
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7560C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413611 | ||||||
| chr17:44413613
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7562G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413613 | ||||||
| chr17:44413614
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7563G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413614 | ||||||
| chr17:44413616
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7565A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413616 | ||||||
| chr17:44413619
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7568T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413619 | ||||||
| chr17:44413620
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7569A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413620 | ||||||
| chr17:44413621
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0145 | 3 | HG02148.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.493-7570C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413621 | ||||||
| chr17:44413762
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0089 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.493-7711C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413762 | ||||||
| chr17:44413974
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.493-7923A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44413974 | ||||||
| chr17:44414005
|
T | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(292): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.493-7954A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414005 | ||||||
| chr17:44414058
|
C | CAT | 14 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0066others(11): Show | 14 | HG01358.hp1 HG02074.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.493-8009_493-8008d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414058 | ||||||
| chr17:44414058
|
C | CATAT | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01243.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-8011_493-8008d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414058 | ||||||
| chr17:44414058
|
CAT | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0119a0001c0002t0001g0207others(1): Show | 4 | HG00423.hp2 HG00621.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-8009_493-8008d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414058 | ||||||
| chr17:44414058
|
CATAT | C | 166 | a0001c0001t0001g0078a0001c0001t0001g0158a0001c0001t0001g0159others(163): Show | 166 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.493-8011_493-8008d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414058 | ||||||
| chr17:44414077
|
A | G | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.493-8026T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414077 | ||||||
| chr17:44414079
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(33): Show | 36 | HG01169.hp1 HG02280.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.493-8028T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414079 | ||||||
| chr17:44414087
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.493-8036C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414087 | ||||||
| chr17:44414089
|
A | G | 10 | a0001c0001t0001g0072a0001c0003t0001g0144a0001c0003t0001g0166others(7): Show | 10 | HG04199.hp1 NA18946.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.493-8038T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414089 | ||||||
| chr17:44414099
|
A | G | 4 | a0001c0001t0001g0064a0001c0008t0013g0164a0003c0006t0001g0239others(1): Show | 4 | HG01261.hp1 HG01496.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-8048T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414099 | ||||||
| chr17:44414101
|
G | A | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-8050C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414101 | ||||||
| chr17:44414107
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-8056T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414107 | ||||||
| chr17:44414115
|
A | ATGTATAT others(21): Show |
13 | a0001c0001t0001g0037a0001c0001t0001g0183a0001c0001t0001g0184others(10): Show | 13 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.493-8092_493-8065d others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414115 | ||||||
| chr17:44414115
|
A | ATGTATAT others(37): Show |
1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.493-8065_493-8064i others(46): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414115 | ||||||
| chr17:44414117
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493-8082_493-8067d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414117 | ||||||
| chr17:44414117
|
GTATATAT others(11): Show |
G | 127 | a0001c0001t0001g0078a0001c0002t0001g0002a0001c0002t0001g0156others(124): Show | 127 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.493-8084_493-8067d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414117 | ||||||
| chr17:44414125
|
A | G | 22 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(19): Show | 22 | HG00408.hp1 HG01261.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.493-8074T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414125 | ||||||
| chr17:44414129
|
G | A | 15 | a0001c0002t0001g0208a0001c0002t0001g0210a0001c0002t0001g0211others(12): Show | 15 | HG00408.hp1 HG01261.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.493-8078C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414129 | ||||||
| chr17:44414129
|
GTA | G | 12 | a0001c0001t0001g0030a0001c0001t0001g0082a0001c0001t0001g0085others(9): Show | 12 | HG02055.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-8080_493-8079d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414129 | ||||||
| chr17:44414131
|
A | G | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.493-8080T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414131 | ||||||
| chr17:44414131
|
ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0058a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-8094_493-8081d others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414131 | ||||||
| chr17:44414133
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.493-8082T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414133 | ||||||
| chr17:44414137
|
ATATATG | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-8092_493-8087d others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414137 | ||||||
| chr17:44414139
|
ATATGTGT others(11): Show |
A | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.493-8106_493-8089d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414139 | ||||||
| chr17:44414141
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 4 | NA18941.hp2 NA18946.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-8090T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414141 | ||||||
| chr17:44414141
|
ATGTGTAT others(9): Show |
A | 20 | a0001c0001t0001g0158a0001c0002t0001g0208a0001c0002t0001g0210others(17): Show | 20 | HG00408.hp1 HG01261.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.493-8106_493-8091d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414141 | ||||||
| chr17:44414145
|
G | A | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.493-8094C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414145 | ||||||
| chr17:44414145
|
GTATATAT others(9): Show |
G | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.493-8110_493-8095d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414145 | ||||||
| chr17:44414147
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0193 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.493-8097_493-8096i others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414147 | ||||||
| chr17:44414147
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.493-8096T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414147 | ||||||
| chr17:44414149
|
ATATATAT others(3): Show |
A | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.493-8108_493-8099d others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414149 | ||||||
| chr17:44414157
|
G | A | 132 | a0001c0001t0001g0078a0001c0001t0001g0157a0001c0001t0001g0159others(129): Show | 132 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.493-8106C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414157 | ||||||
| chr17:44414159
|
G | GTA | 3 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0007g0096 | 3 | HG00323.hp2 HG02572.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.493-8110_493-8109d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414159 | ||||||
| chr17:44414161
|
A | G | 28 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.493-8110T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414161 | ||||||
| chr17:44414177
|
A | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.493-8126T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414177 | ||||||
| chr17:44414545
|
G | A | 1 | a0001c0002t0002g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.493-8494C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44414545 | ||||||
| chr17:44415093
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.493-9042A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415093 | ||||||
| chr17:44415188
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.493-9137G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415188 | ||||||
| chr17:44415304
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.492+9045A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415304 | ||||||
| chr17:44415320
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.492+9029G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415320 | ||||||
| chr17:44415427
|
C | A | 4 | a0001c0002t0001g0205a0001c0002t0001g0235a0001c0002t0001g0240others(1): Show | 4 | HG02735.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+8922G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415427 | ||||||
| chr17:44415492
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.492+8857T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415492 | ||||||
| chr17:44415515
|
T | A | 2 | a0001c0002t0001g0227a0001c0002t0001g0243 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.492+8834A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415515 | ||||||
| chr17:44415573
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.492+8776T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415573 | ||||||
| chr17:44415652
|
A | C | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.492+8697T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415652 | ||||||
| chr17:44415748
|
C | T | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.492+8601G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415748 | ||||||
| chr17:44415813
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.492+8536C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415813 | ||||||
| chr17:44415852
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.492+8497C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415852 | ||||||
| chr17:44415888
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.492+8461T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44415888 | ||||||
| chr17:44416127
|
G | A | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.492+8222C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416127 | ||||||
| chr17:44416143
|
A | C | 1 | a0001c0002t0001g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.492+8206T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416143 | ||||||
| chr17:44416247
|
G | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0103others(15): Show | 18 | HG00621.hp2 HG00738.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.492+8102C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416247 | ||||||
| chr17:44416262
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.492+8087G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416262 | ||||||
| chr17:44416319
|
AT | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.492+8029delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416319 | ||||||
| chr17:44416358
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0050 | 3 | NA18950.hp1 NA18977.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.492+7991A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416358 | ||||||
| chr17:44416487
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+7862C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416487 | ||||||
| chr17:44416509
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.492+7840G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416509 | ||||||
| chr17:44416652
|
A | G | 1 | a0002c0005t0001g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.492+7697T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416652 | ||||||
| chr17:44416817
|
G | A | 53 | a0001c0002t0001g0167a0001c0002t0001g0198a0001c0002t0001g0202others(50): Show | 53 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.492+7532C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44416817 | ||||||
| chr17:44417299
|
A | G | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+7050T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417299 | ||||||
| chr17:44417340
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.492+7009A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417340 | ||||||
| chr17:44417343
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.492+7006G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417343 | ||||||
| chr17:44417466
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.492+6883C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417466 | ||||||
| chr17:44417571
|
GACT | G | 3 | a0001c0003t0001g0174a0001c0003t0001g0175a0001c0003t0001g0178 | 3 | NA18957.hp1 NA18977.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.492+6775_492+6777d others(5): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417571 | ||||||
| chr17:44417764
|
G | A | 1 | a0001c0002t0001g0268 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.492+6585C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417764 | ||||||
| chr17:44417913
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0124 | 2 | NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.492+6436G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44417913 | ||||||
| chr17:44418166
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+6183C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418166 | ||||||
| chr17:44418170
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+6179T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418170 | ||||||
| chr17:44418322
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.492+6027G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418322 | ||||||
| chr17:44418456
|
C | CT | 13 | a0001c0001t0001g0050a0001c0001t0001g0195a0001c0002t0001g0156others(10): Show | 13 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.492+5892dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418456 | ||||||
| chr17:44418456
|
CT | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0154others(26): Show | 29 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.492+5892delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418456 | ||||||
| chr17:44418537
|
T | G | 1 | a0001c0002t0001g0224 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.492+5812A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418537 | ||||||
| chr17:44418578
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.492+5771G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418578 | ||||||
| chr17:44418612
|
G | A | 1 | a0003c0006t0001g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.492+5737C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418612 | ||||||
| chr17:44418620
|
T | G | 1 | a0001c0002t0001g0246 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.492+5729A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418620 | ||||||
| chr17:44418627
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.492+5722T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418627 | ||||||
| chr17:44418642
|
G | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+5707C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418642 | ||||||
| chr17:44418731
|
G | A | 2 | a0001c0002t0004g0273a0001c0002t0004g0274 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.492+5618C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44418731 | ||||||
| chr17:44419560
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.492+4789A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419560 | ||||||
| chr17:44419658
|
A | AG | 5 | a0001c0002t0001g0204a0001c0002t0001g0213a0001c0002t0001g0256others(2): Show | 5 | HG00642.hp2 HG00673.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+4690_492+4691i others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419658 | ||||||
| chr17:44419659
|
A | AT | 8 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0158others(5): Show | 8 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+4689dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419659 | ||||||
| chr17:44419659
|
A | G | 139 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(136): Show | 139 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.492+4690T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419659 | ||||||
| chr17:44419659
|
A | T | 5 | a0001c0002t0001g0204a0001c0002t0001g0213a0001c0002t0001g0256others(2): Show | 5 | HG00642.hp2 HG00673.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+4690T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419659 | ||||||
| chr17:44419660
|
T | G | 1 | a0001c0002t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.492+4689A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419660 | ||||||
| chr17:44419671
|
T | A | 3 | a0001c0002t0001g0292a0001c0002t0001g0294a0001c0002t0001g0303 | 3 | HG01243.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.492+4678A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419671 | ||||||
| chr17:44419706
|
G | A | 1 | a0001c0012t0001g0297 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.492+4643C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419706 | ||||||
| chr17:44419711
|
G | A | 1 | a0001c0002t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.492+4638C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419711 | ||||||
| chr17:44419832
|
T | A | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.492+4517A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44419832 | ||||||
| chr17:44420008
|
C | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.492+4341G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420008 | ||||||
| chr17:44420038
|
G | GT | 13 | a0001c0001t0001g0066a0001c0001t0001g0183a0001c0001t0001g0191others(10): Show | 13 | HG00673.hp1 HG01255.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.492+4310dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420038 | ||||||
| chr17:44420038
|
GT | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.492+4310delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420038 | ||||||
| chr17:44420058
|
G | A | 1 | a0001c0002t0001g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.492+4291C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420058 | ||||||
| chr17:44420065
|
G | C | 28 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.492+4284C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420065 | ||||||
| chr17:44420149
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.492+4200T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420149 | ||||||
| chr17:44420326
|
G | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+4023C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420326 | ||||||
| chr17:44420369
|
G | A | 160 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(157): Show | 160 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.492+3980C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420369 | ||||||
| chr17:44420779
|
T | C | 1 | a0001c0002t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.492+3570A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44420779 | ||||||
| chr17:44421068
|
T | C | 3 | a0001c0002t0001g0292a0001c0002t0001g0294a0001c0002t0001g0303 | 3 | HG01243.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.492+3281A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421068 | ||||||
| chr17:44421095
|
G | GCC | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+3252_492+3253d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421095 | ||||||
| chr17:44421255
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+3094G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421255 | ||||||
| chr17:44421270
|
G | C | 1 | a0001c0002t0001g0261 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.492+3079C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421270 | ||||||
| chr17:44421277
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.492+3072C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421277 | ||||||
| chr17:44421310
|
C | T | 3 | a0001c0002t0001g0198a0001c0002t0001g0261a0001c0002t0001g0304 | 3 | HG00741.hp2 HG01496.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.492+3039G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421310 | ||||||
| chr17:44421369
|
T | C | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.492+2980A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421369 | ||||||
| chr17:44421397
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492+2952C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421397 | ||||||
| chr17:44421516
|
C | T | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.492+2833G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421516 | ||||||
| chr17:44421654
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+2695C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421654 | ||||||
| chr17:44421711
|
CCTTT | C | 4 | a0001c0002t0001g0319a0001c0002t0001g0320a0001c0002t0001g0322others(1): Show | 4 | HG01069.hp2 HG01169.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+2634_492+2637d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421711 | ||||||
| chr17:44421724
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.492+2625A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421724 | ||||||
| chr17:44421733
|
C | CT | 10 | a0001c0001t0001g0148a0001c0002t0001g0011a0001c0002t0001g0012others(7): Show | 10 | HG01109.hp2 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.492+2615dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421733 | ||||||
| chr17:44421745
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+2604C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421745 | ||||||
| chr17:44421764
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.492+2585A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421764 | ||||||
| chr17:44421775
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.492+2574C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421775 | ||||||
| chr17:44421785
|
G | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.492+2564C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421785 | ||||||
| chr17:44421872
|
G | A | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.492+2477C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44421872 | ||||||
| chr17:44422040
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.492+2309G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422040 | ||||||
| chr17:44422359
|
T | A | 1 | a0001c0002t0014g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.492+1990A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422359 | ||||||
| chr17:44422465
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.492+1884G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422465 | ||||||
| chr17:44422494
|
A | G | 13 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(10): Show | 13 | HG01975.hp2 HG01978.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.492+1855T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422494 | ||||||
| chr17:44422567
|
G | T | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.492+1782C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422567 | ||||||
| chr17:44422710
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+1639G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422710 | ||||||
| chr17:44422811
|
A | T | 1 | a0001c0002t0001g0271 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.492+1538T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422811 | ||||||
| chr17:44422994
|
C | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+1355G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44422994 | ||||||
| chr17:44423042
|
G | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+1307C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423042 | ||||||
| chr17:44423044
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0025others(73): Show | 77 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.492+1305C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423044 | ||||||
| chr17:44423176
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+1173C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423176 | ||||||
| chr17:44423219
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.492+1130C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423219 | ||||||
| chr17:44423234
|
C | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.492+1115G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423234 | ||||||
| chr17:44423459
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.492+890A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423459 | ||||||
| chr17:44423742
|
C | G | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+607G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423742 | ||||||
| chr17:44423756
|
T | TG | 13 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0066others(10): Show | 13 | HG00438.hp1 HG01243.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.492+592dupC | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423756 | ||||||
| chr17:44423764
|
C | T | 1 | a0001c0003t0001g0180 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.492+585G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423764 | ||||||
| chr17:44423767
|
C | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+582G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423767 | ||||||
| chr17:44423820
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.492+529A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423820 | ||||||
| chr17:44423829
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.492+520T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423829 | ||||||
| chr17:44423839
|
G | C | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.492+510C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423839 | ||||||
| chr17:44423842
|
A | G | 1 | a0001c0002t0010g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.492+507T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423842 | ||||||
| chr17:44423904
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+445A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44423904 | ||||||
| chr17:44424014
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.492+335G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44424014 | ||||||
| chr17:44424158
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.492+191A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44424158 | ||||||
| chr17:44424324
|
C | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.492+25G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 6/7 | chr17 | 44424324 | ||||||
| chr17:44424760
|
CAAAAAAT | C | 3 | a0001c0002t0001g0215a0001c0002t0001g0256a0001c0002t0001g0260 | 3 | HG00639.hp1 HG01106.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.349-275_349-269del others(7): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44424760 | ||||||
| chr17:44424761
|
A | C | 157 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(154): Show | 157 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.349-269T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44424761 | ||||||
| chr17:44425022
|
AAAC | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.349-533_349-531del others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425022 | ||||||
| chr17:44425226
|
A | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.349-734T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425226 | ||||||
| chr17:44425255
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349-763C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425255 | ||||||
| chr17:44425511
|
C | T | 1 | a0001c0002t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-1019G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425511 | ||||||
| chr17:44425676
|
G | A | 3 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300 | 3 | HG02258.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.349-1184C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425676 | ||||||
| chr17:44425708
|
T | G | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.349-1216A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425708 | ||||||
| chr17:44425912
|
T | C | 1 | a0001c0001t0015g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.349-1420A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44425912 | ||||||
| chr17:44426357
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.349-1865G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426357 | ||||||
| chr17:44426603
|
C | CA | 174 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(171): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.349-2112dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426603 | ||||||
| chr17:44426603
|
C | CAA | 26 | a0001c0001t0001g0059a0001c0001t0001g0108a0001c0001t0001g0113others(23): Show | 26 | HG00423.hp1 HG02071.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.349-2113_349-2112d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426603 | ||||||
| chr17:44426662
|
A | G | 3 | a0001c0002t0001g0292a0001c0002t0001g0294a0001c0002t0001g0303 | 3 | HG01243.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.349-2170T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426662 | ||||||
| chr17:44426705
|
T | C | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.349-2213A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426705 | ||||||
| chr17:44426835
|
AAC | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-2345_349-2344d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426835 | ||||||
| chr17:44426846
|
ACACT | A | 20 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(17): Show | 20 | HG01243.hp2 HG02040.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.349-2358_349-2355d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426846 | ||||||
| chr17:44426846
|
ACACTCT | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0002t0001g0002others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.349-2360_349-2355d others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426846 | ||||||
| chr17:44426846
|
ACACTCTC others(3): Show |
A | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.349-2364_349-2355d others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426846 | ||||||
| chr17:44426848
|
A | ACT | 4 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0117others(1): Show | 4 | HG02040.hp1 HG02071.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2358_349-2357d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426848 | ||||||
| chr17:44426848
|
A | T | 4 | a0001c0001t0001g0073a0001c0002t0001g0229a0001c0002t0002g0004others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2356T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426848 | ||||||
| chr17:44426848
|
ACTCT | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0126a0001c0001t0001g0128others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-2360_349-2357d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426848 | ||||||
| chr17:44426848
|
ACTCTCT | A | 4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0196others(1): Show | 4 | HG01175.hp2 HG03831.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2362_349-2357d others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426848 | ||||||
| chr17:44426848
|
ACTCTCTC others(11): Show |
A | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.349-2374_349-2357d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426848 | ||||||
| chr17:44426850
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-2358A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44426850 | ||||||
| chr17:44427081
|
A | AT | 25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0103others(22): Show | 25 | HG00621.hp2 HG00738.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.349-2590dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427081 | ||||||
| chr17:44427081
|
A | T | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.349-2589T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427081 | ||||||
| chr17:44427158
|
A | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.349-2666T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427158 | ||||||
| chr17:44427327
|
A | C | 1 | a0001c0001t0001g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.349-2835T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427327 | ||||||
| chr17:44427511
|
A | G | 6 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-3019T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427511 | ||||||
| chr17:44427801
|
G | C | 1 | a0001c0002t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.349-3309C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427801 | ||||||
| chr17:44427832
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.349-3340C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44427832 | ||||||
| chr17:44428143
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.349-3651G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428143 | ||||||
| chr17:44428206
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.349-3714A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428206 | ||||||
| chr17:44428207
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.349-3715G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428207 | ||||||
| chr17:44428394
|
G | A | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349-3902C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428394 | ||||||
| chr17:44428447
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0116 | 2 | NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.349-3955G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428447 | ||||||
| chr17:44428456
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.349-3964C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428456 | ||||||
| chr17:44428587
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349-4095C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428587 | ||||||
| chr17:44428657
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.349-4165C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428657 | ||||||
| chr17:44428717
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349-4225G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428717 | ||||||
| chr17:44428766
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.349-4274G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428766 | ||||||
| chr17:44428767
|
G | A | 13 | a0001c0001t0001g0029a0001c0003t0001g0144a0001c0003t0001g0166others(10): Show | 13 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-4275C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428767 | ||||||
| chr17:44428872
|
T | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.349-4380A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428872 | ||||||
| chr17:44428910
|
G | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.349-4418C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428910 | ||||||
| chr17:44428917
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-4425C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44428917 | ||||||
| chr17:44429001
|
C | T | 1 | a0001c0002t0006g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.349-4509G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429001 | ||||||
| chr17:44429029
|
T | C | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.349-4537A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429029 | ||||||
| chr17:44429157
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.349-4665G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429157 | ||||||
| chr17:44429360
|
T | C | 1 | a0001c0002t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.349-4868A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429360 | ||||||
| chr17:44429402
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-4910A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429402 | ||||||
| chr17:44429460
|
A | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.349-4968T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429460 | ||||||
| chr17:44429471
|
A | G | 5 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171others(2): Show | 5 | HG01099.hp2 HG01168.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-4979T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429471 | ||||||
| chr17:44429478
|
T | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(22): Show | 25 | HG00280.hp1 HG00673.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.349-4986A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429478 | ||||||
| chr17:44429592
|
C | T | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.349-5100G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429592 | ||||||
| chr17:44429614
|
A | G | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5122T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429614 | ||||||
| chr17:44429647
|
T | TACACACA others(11): Show |
1 | a0001c0002t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.349-5156_349-5155i others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429647 | ||||||
| chr17:44429649
|
A | AAC | 15 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0046others(12): Show | 15 | HG00099.hp1 HG00438.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-5159_349-5158d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACAC | 23 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(20): Show | 23 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.349-5161_349-5158d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(1): Show |
5 | a0001c0002t0001g0156a0001c0002t0001g0168a0001c0002t0001g0172others(2): Show | 5 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-5165_349-5158d others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(5): Show |
1 | a0001c0002t0001g0316 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.349-5169_349-5158d others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(7): Show |
4 | a0001c0002t0001g0291a0001c0002t0001g0298a0001c0002t0001g0299others(1): Show | 4 | HG02258.hp2 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-5171_349-5158d others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(9): Show |
29 | a0001c0002t0001g0205a0001c0002t0001g0210a0001c0002t0001g0211others(26): Show | 29 | HG00673.hp1 HG01358.hp2 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-5173_349-5158d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(11): Show |
28 | a0001c0002t0001g0167a0001c0002t0001g0198a0001c0002t0001g0206others(25): Show | 28 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.349-5175_349-5158d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(13): Show |
35 | a0001c0002t0001g0002a0001c0002t0001g0204a0001c0002t0001g0209others(32): Show | 35 | HG01069.hp1 HG01069.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.349-5177_349-5158d others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(15): Show |
22 | a0001c0002t0001g0203a0001c0002t0001g0212a0001c0002t0001g0220others(19): Show | 22 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.349-5179_349-5158d others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(17): Show |
4 | a0001c0002t0001g0233a0001c0002t0001g0253a0001c0002t0001g0313others(1): Show | 4 | HG01168.hp2 HG03831.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-5181_349-5158d others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(19): Show |
2 | a0001c0002t0001g0309a0001c0002t0001g0310 | 2 | HG00438.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.349-5183_349-5158d others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | AACACACA others(21): Show |
1 | a0001c0002t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.349-5185_349-5158d others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | ACACACAC others(6): Show |
1 | a0001c0002t0001g0271 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.349-5158_349-5157i others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | ACACACAC others(12): Show |
2 | a0001c0002t0001g0224a0001c0002t0001g0247 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.349-5158_349-5157i others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
A | C | 1 | a0001c0002t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.349-5157T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
AAC | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0025others(67): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.349-5159_349-5158d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429649
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.349-5173_349-5158d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429649 | ||||||
| chr17:44429683
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.349-5191G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429683 | ||||||
| chr17:44429685
|
C | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-5193G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429685 | ||||||
| chr17:44429686
|
A | ACACACAC others(10): Show |
2 | a0001c0003t0001g0178a0003c0006t0001g0239 | 2 | HG01496.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.349-5195_349-5194i others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429686 | ||||||
| chr17:44429686
|
A | ACACACAC others(12): Show |
2 | a0001c0002t0001g0222a0001c0003t0001g0177 | 2 | HG01074.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.349-5195_349-5194i others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429686 | ||||||
| chr17:44429686
|
A | ACACACAC others(14): Show |
1 | a0001c0002t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.349-5195_349-5194i others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429686 | ||||||
| chr17:44429686
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.349-5194T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429686 | ||||||
| chr17:44429687
|
A | AC | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-5196_349-5195i others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429687 | ||||||
| chr17:44429688
|
A | C | 3 | a0001c0001t0001g0148a0001c0002t0001g0302a0003c0006t0001g0242 | 3 | HG01261.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.349-5196T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429688 | ||||||
| chr17:44429689
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.349-5197T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429689 | ||||||
| chr17:44429690
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.349-5198G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429690 | ||||||
| chr17:44429690
|
C | CA | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-5199dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429690 | ||||||
| chr17:44429690
|
CAACA | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-5202_349-5199d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429690 | ||||||
| chr17:44429693
|
C | A | 1 | a0003c0006t0001g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.349-5201G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429693 | ||||||
| chr17:44429695
|
A | C | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-5203T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429695 | ||||||
| chr17:44429701
|
C | A | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-5209G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429701 | ||||||
| chr17:44429702
|
A | C | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-5210T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429702 | ||||||
| chr17:44429713
|
A | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349-5221T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429713 | ||||||
| chr17:44429734
|
C | T | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-5242G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429734 | ||||||
| chr17:44429809
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.348+5256T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429809 | ||||||
| chr17:44429833
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+5232G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429833 | ||||||
| chr17:44429842
|
T | A | 1 | a0001c0002t0001g0286 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.348+5223A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429842 | ||||||
| chr17:44429862
|
T | TA | 19 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0025others(16): Show | 19 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+5202dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429862 | ||||||
| chr17:44429938
|
A | T | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.348+5127T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429938 | ||||||
| chr17:44429942
|
T | C | 8 | a0001c0001t0001g0195a0001c0002t0001g0011a0001c0002t0001g0012others(5): Show | 8 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+5123A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429942 | ||||||
| chr17:44429978
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.348+5087T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429978 | ||||||
| chr17:44429994
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.348+5071G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44429994 | ||||||
| chr17:44430009
|
GAGCAAGA others(12): Show |
G | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.348+5037_348+5055d others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430009 | ||||||
| chr17:44430370
|
TCAATGTA others(11): Show |
T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.348+4677_348+4694d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430370 | ||||||
| chr17:44430476
|
C | T | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.348+4589G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430476 | ||||||
| chr17:44430542
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.348+4523A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430542 | ||||||
| chr17:44430613
|
A | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+4452T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430613 | ||||||
| chr17:44430645
|
A | AT | 12 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0090others(9): Show | 13 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+4419dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430645 | ||||||
| chr17:44430742
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.348+4323T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430742 | ||||||
| chr17:44430806
|
C | CT | 142 | a0001c0001t0001g0121a0001c0002t0001g0002a0001c0002t0001g0156others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.348+4258dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44430806 | ||||||
| chr17:44431092
|
C | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.348+3973G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431092 | ||||||
| chr17:44431108
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG00280.hp1 NA18941.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+3957G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431108 | ||||||
| chr17:44431366
|
T | A | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.348+3699A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431366 | ||||||
| chr17:44431378
|
G | GA | 89 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+3686dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431378 | ||||||
| chr17:44431378
|
G | GAA | 13 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0001g0082others(10): Show | 13 | HG01243.hp2 HG02922.hp2 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+3685_348+3686d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431378 | ||||||
| chr17:44431378
|
GA | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02615.hp2 HG03139.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+3686delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431378 | ||||||
| chr17:44431573
|
A | ATT | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.348+3491_348+3492i others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431573 | ||||||
| chr17:44431904
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.348+3161G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44431904 | ||||||
| chr17:44432010
|
A | T | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+3055T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432010 | ||||||
| chr17:44432013
|
A | G | 2 | a0001c0002t0001g0214a0001c0002t0001g0230 | 2 | NA18959.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.348+3052T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432013 | ||||||
| chr17:44432047
|
G | GT | 8 | a0001c0001t0001g0051a0001c0001t0001g0087a0001c0001t0001g0099others(5): Show | 8 | HG01978.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+3017dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432047 | ||||||
| chr17:44432047
|
GT | G | 25 | a0001c0001t0001g0024a0001c0001t0001g0082a0001c0001t0001g0085others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.348+3017delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432047 | ||||||
| chr17:44432295
|
G | A | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+2770C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432295 | ||||||
| chr17:44432303
|
T | C | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+2762A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432303 | ||||||
| chr17:44432309
|
G | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.348+2756C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432309 | ||||||
| chr17:44432459
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0015g0141 | 2 | HG01993.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.348+2606G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432459 | ||||||
| chr17:44432553
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.348+2512G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432553 | ||||||
| chr17:44432622
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.348+2443C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432622 | ||||||
| chr17:44432820
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.348+2245T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432820 | ||||||
| chr17:44432893
|
C | T | 1 | a0001c0004t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.348+2172G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44432893 | ||||||
| chr17:44433143
|
C | A | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.348+1922G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433143 | ||||||
| chr17:44433162
|
A | T | 1 | a0001c0001t0015g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.348+1903T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433162 | ||||||
| chr17:44433480
|
T | G | 5 | a0001c0002t0001g0011a0001c0002t0001g0013a0001c0002t0001g0015others(2): Show | 5 | HG02809.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+1585A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433480 | ||||||
| chr17:44433563
|
T | C | 1 | a0002c0005t0001g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.348+1502A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433563 | ||||||
| chr17:44433592
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.348+1473G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433592 | ||||||
| chr17:44433617
|
G | C | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.348+1448C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433617 | ||||||
| chr17:44433627
|
G | A | 2 | a0001c0002t0001g0221a0001c0002t0001g0231 | 2 | NA18939.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.348+1438C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433627 | ||||||
| chr17:44433628
|
A | G | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.348+1437T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433628 | ||||||
| chr17:44433705
|
G | C | 1 | a0001c0002t0001g0211 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.348+1360C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433705 | ||||||
| chr17:44433843
|
A | T | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.348+1222T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433843 | ||||||
| chr17:44433848
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+1217C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433848 | ||||||
| chr17:44433854
|
G | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1211C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44433854 | ||||||
| chr17:44434006
|
T | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.348+1059A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44434006 | ||||||
| chr17:44434009
|
C | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.348+1056G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44434009 | ||||||
| chr17:44434150
|
A | G | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.348+915T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44434150 | ||||||
| chr17:44434314
|
A | G | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.348+751T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44434314 | ||||||
| chr17:44434372
|
C | T | 3 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300 | 3 | HG02258.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.348+693G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 5/7 | chr17 | 44434372 | ||||||
| chr17:44435190
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.262-39C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435190 | ||||||
| chr17:44435312
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.262-161G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435312 | ||||||
| chr17:44435372
|
T | C | 1 | a0001c0002t0001g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.262-221A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435372 | ||||||
| chr17:44435411
|
C | CT | 121 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(118): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.262-261dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435411 | ||||||
| chr17:44435411
|
C | CTT | 29 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0115others(26): Show | 29 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.262-262_262-261dup others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435411 | ||||||
| chr17:44435411
|
C | CTTT | 118 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.262-263_262-261dup others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435411 | ||||||
| chr17:44435411
|
CT | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0001g0135others(3): Show | 6 | HG01175.hp1 HG02015.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-261delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435411 | ||||||
| chr17:44435413
|
T | TC | 14 | a0001c0001t0001g0003a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-263_262-262ins others(1): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435413 | ||||||
| chr17:44435414
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0162 | 2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.262-263A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435414 | ||||||
| chr17:44435562
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-411G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435562 | ||||||
| chr17:44435605
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-454A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435605 | ||||||
| chr17:44435668
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.262-517G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435668 | ||||||
| chr17:44435782
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-631C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435782 | ||||||
| chr17:44435787
|
C | T | 1 | a0001c0001t0011g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.262-636G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435787 | ||||||
| chr17:44435878
|
C | T | 1 | a0001c0002t0001g0315 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.261+600G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435878 | ||||||
| chr17:44435892
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.261+586A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435892 | ||||||
| chr17:44435995
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.261+483G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44435995 | ||||||
| chr17:44436003
|
T | C | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.261+475A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436003 | ||||||
| chr17:44436029
|
C | CA | 144 | a0001c0001t0001g0033a0001c0001t0001g0057a0001c0001t0001g0063others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.261+448dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436029 | ||||||
| chr17:44436029
|
C | CAA | 8 | a0001c0001t0001g0071a0001c0001t0001g0115a0001c0002t0001g0203others(5): Show | 8 | HG02486.hp1 HG02602.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+447_261+448dup others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436029 | ||||||
| chr17:44436029
|
CA | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0046others(13): Show | 16 | HG00323.hp2 HG01255.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.261+448delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436029 | ||||||
| chr17:44436029
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.261+436_261+448del others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436029 | ||||||
| chr17:44436081
|
T | C | 5 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(2): Show | 5 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+397A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436081 | ||||||
| chr17:44436107
|
C | T | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.261+371G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 4/7 | chr17 | 44436107 | ||||||
| chr17:44436746
|
A | AC | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-202dupG | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44436746 | ||||||
| chr17:44436748
|
G | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-203C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44436748 | ||||||
| chr17:44436891
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-346C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44436891 | ||||||
| chr17:44436929
|
A | C | 1 | a0001c0002t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.194-384T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44436929 | ||||||
| chr17:44436986
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-441A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44436986 | ||||||
| chr17:44437214
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.194-669A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437214 | ||||||
| chr17:44437487
|
C | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.194-942G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437487 | ||||||
| chr17:44437532
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-987A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437532 | ||||||
| chr17:44437657
|
CA | C | 91 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.194-1113delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437657 | ||||||
| chr17:44437667
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.194-1122A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437667 | ||||||
| chr17:44437945
|
G | GA | 18 | a0001c0001t0001g0087a0001c0001t0001g0117a0001c0001t0001g0157others(15): Show | 18 | HG02071.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.194-1401dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437945 | ||||||
| chr17:44437955
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.194-1410T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437955 | ||||||
| chr17:44437959
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.194-1414T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437959 | ||||||
| chr17:44437959
|
AC | A | 142 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(139): Show | 142 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.194-1415delG | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437959 | ||||||
| chr17:44437960
|
C | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(33): Show | 36 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.194-1415G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437960 | ||||||
| chr17:44437963
|
A | C | 125 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.194-1418T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437963 | ||||||
| chr17:44437982
|
C | T | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-1437G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44437982 | ||||||
| chr17:44438152
|
A | G | 1 | a0001c0002t0001g0224 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.194-1607T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438152 | ||||||
| chr17:44438532
|
C | G | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194-1987G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438532 | ||||||
| chr17:44438592
|
C | T | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.194-2047G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438592 | ||||||
| chr17:44438730
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(292): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.194-2185A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438730 | ||||||
| chr17:44438794
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.194-2249C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438794 | ||||||
| chr17:44438871
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.194-2326C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438871 | ||||||
| chr17:44438957
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0091 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.194-2412C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44438957 | ||||||
| chr17:44439542
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.194-2997C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439542 | ||||||
| chr17:44439697
|
C | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-3152G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439697 | ||||||
| chr17:44439714
|
T | C | 1 | a0001c0002t0001g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.194-3169A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439714 | ||||||
| chr17:44439783
|
CT | C | 18 | a0001c0001t0001g0095a0001c0001t0001g0159a0001c0001t0001g0160others(15): Show | 18 | HG00408.hp1 HG02922.hp2 HG03041.hp1 others(15): Show |
intron_variant | MODIFIER | c.194-3239delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439783 | ||||||
| chr17:44439814
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194-3269C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439814 | ||||||
| chr17:44439971
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-3426G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439971 | ||||||
| chr17:44439986
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.194-3441A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44439986 | ||||||
| chr17:44440035
|
G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(21): Show | 24 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.194-3490C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440035 | ||||||
| chr17:44440089
|
C | A | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.194-3544G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440089 | ||||||
| chr17:44440099
|
T | C | 2 | a0001c0002t0004g0273a0001c0002t0004g0274 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.194-3554A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440099 | ||||||
| chr17:44440194
|
T | G | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.194-3649A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440194 | ||||||
| chr17:44440408
|
C | A | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.194-3863G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440408 | ||||||
| chr17:44440504
|
C | G | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-3959G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440504 | ||||||
| chr17:44440551
|
G | A | 2 | a0001c0001t0011g0023a0001c0010t0001g0134 | 2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.194-4006C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440551 | ||||||
| chr17:44440560
|
G | C | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.194-4015C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440560 | ||||||
| chr17:44440859
|
A | AT | 13 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.194-4315dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44440859 | ||||||
| chr17:44441390
|
C | CT | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.194-4846dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44441390 | ||||||
| chr17:44441636
|
A | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-5091T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44441636 | ||||||
| chr17:44441707
|
C | T | 1 | a0001c0002t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-5162G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44441707 | ||||||
| chr17:44441750
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.194-5205G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44441750 | ||||||
| chr17:44441959
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.194-5414G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44441959 | ||||||
| chr17:44442085
|
G | GTATA | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-5544_194-5541d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442085 | ||||||
| chr17:44442108
|
C | CAT | 15 | a0001c0001t0001g0027a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 15 | HG00621.hp2 HG00738.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.194-5565_194-5564d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442108 | ||||||
| chr17:44442108
|
CAT | C | 151 | a0001c0001t0001g0031a0001c0001t0001g0157a0001c0001t0001g0158others(148): Show | 151 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.194-5565_194-5564d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442108 | ||||||
| chr17:44442120
|
T | G | 18 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0085others(15): Show | 18 | HG00408.hp2 HG00741.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.194-5575A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442120 | ||||||
| chr17:44442120
|
TATAG | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01243.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-5579_194-5576d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442120 | ||||||
| chr17:44442122
|
T | G | 156 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.194-5577A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442122 | ||||||
| chr17:44442122
|
T | TAG | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0140 | 3 | HG01993.hp1 NA18982.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.194-5579_194-5578d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442122 | ||||||
| chr17:44442122
|
TAG | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG03041.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-5579_194-5578d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442122 | ||||||
| chr17:44442122
|
TAGAG | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-5581_194-5578d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442122 | ||||||
| chr17:44442124
|
G | T | 39 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0036others(36): Show | 39 | HG00621.hp2 HG01975.hp2 HG02083.hp1 others(36): Show |
intron_variant | MODIFIER | c.194-5579C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442124 | ||||||
| chr17:44442126
|
G | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0077a0001c0001t0001g0103others(3): Show | 6 | HG01975.hp2 HG02523.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-5581C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442126 | ||||||
| chr17:44442128
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.194-5583C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442128 | ||||||
| chr17:44442180
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.194-5635C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442180 | ||||||
| chr17:44442213
|
T | TA | 129 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0025others(126): Show | 130 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.194-5669dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442213 | ||||||
| chr17:44442213
|
T | TAA | 18 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(15): Show | 18 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.194-5670_194-5669d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442213 | ||||||
| chr17:44442213
|
TA | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0149others(7): Show | 10 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-5669delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442213 | ||||||
| chr17:44442224
|
A | AC | 19 | a0001c0002t0001g0167a0001c0002t0001g0202a0001c0002t0001g0207others(16): Show | 19 | HG00621.hp1 HG00673.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.194-5680_194-5679i others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442224 | ||||||
| chr17:44442229
|
C | A | 1 | a0001c0002t0001g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.194-5684G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442229 | ||||||
| chr17:44442232
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.194-5687G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442232 | ||||||
| chr17:44442248
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0112 | 2 | HG01943.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.194-5703G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442248 | ||||||
| chr17:44442249
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.194-5704C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442249 | ||||||
| chr17:44442344
|
ATGC | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-5802_194-5800d others(5): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442344 | ||||||
| chr17:44442349
|
TAAGCA | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-5809_194-5805d others(7): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442349 | ||||||
| chr17:44442386
|
C | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-5841G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442386 | ||||||
| chr17:44442859
|
C | G | 1 | a0001c0002t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.194-6314G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44442859 | ||||||
| chr17:44443069
|
CCTTGTCG others(11): Show |
C | 1 | a0001c0002t0001g0222 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194-6542_194-6525d others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443069 | ||||||
| chr17:44443094
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194-6549C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443094 | ||||||
| chr17:44443110
|
A | G | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-6565T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443110 | ||||||
| chr17:44443115
|
T | A | 27 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.194-6570A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443115 | ||||||
| chr17:44443325
|
C | T | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-6780G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443325 | ||||||
| chr17:44443626
|
C | T | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-7081G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443626 | ||||||
| chr17:44443667
|
T | C | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.194-7122A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44443667 | ||||||
| chr17:44444012
|
A | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-7467T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444012 | ||||||
| chr17:44444239
|
T | C | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.194-7694A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444239 | ||||||
| chr17:44444254
|
T | TA | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.194-7710dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444254 | ||||||
| chr17:44444363
|
A | ATCAATTT others(34): Show |
1 | a0001c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-7819_194-7818i others(43): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444363 | ||||||
| chr17:44444456
|
A | G | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-7911T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444456 | ||||||
| chr17:44444530
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-7985A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444530 | ||||||
| chr17:44444571
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.194-8026C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444571 | ||||||
| chr17:44444592
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.194-8047C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444592 | ||||||
| chr17:44444782
|
GA | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-8238delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444782 | ||||||
| chr17:44444862
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-8317C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444862 | ||||||
| chr17:44444953
|
T | G | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194-8408A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44444953 | ||||||
| chr17:44445502
|
CT | C | 32 | a0001c0001t0001g0071a0001c0001t0001g0115a0001c0001t0001g0148others(29): Show | 32 | HG00323.hp1 HG01069.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.194-8958delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445502 | ||||||
| chr17:44445502
|
CTT | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-8959_194-8958d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445502 | ||||||
| chr17:44445511
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194-8966A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445511 | ||||||
| chr17:44445514
|
T | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG03239.hp2 HG03831.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-8969A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445514 | ||||||
| chr17:44445518
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-8973G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445518 | ||||||
| chr17:44445539
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0190 | 2 | HG00280.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.194-8994G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445539 | ||||||
| chr17:44445680
|
A | C | 1 | a0001c0002t0001g0268 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.194-9135T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445680 | ||||||
| chr17:44445963
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-9418A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44445963 | ||||||
| chr17:44446090
|
C | T | 4 | a0001c0002t0001g0002a0001c0002t0001g0203a0001c0002t0001g0228others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-9545G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446090 | ||||||
| chr17:44446108
|
TA | T | 10 | a0001c0001t0001g0094a0001c0002t0001g0011a0001c0002t0001g0012others(7): Show | 10 | HG01943.hp2 HG02523.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-9564delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446108 | ||||||
| chr17:44446121
|
A | T | 136 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(133): Show | 136 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.194-9576T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446121 | ||||||
| chr17:44446260
|
G | A | 15 | a0001c0001t0001g0037a0001c0001t0001g0183a0001c0001t0001g0184others(12): Show | 15 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.194-9715C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446260 | ||||||
| chr17:44446337
|
C | T | 1 | a0001c0002t0001g0298 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.194-9792G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446337 | ||||||
| chr17:44446394
|
G | T | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194-9849C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446394 | ||||||
| chr17:44446474
|
A | T | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.194-9929T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446474 | ||||||
| chr17:44446625
|
G | A | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.194-10080C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446625 | ||||||
| chr17:44446835
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.194-10290A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446835 | ||||||
| chr17:44446838
|
A | AT | 7 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0090others(4): Show | 8 | HG00323.hp2 HG01081.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-10294dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446838 | ||||||
| chr17:44446838
|
AT | A | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.194-10294delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44446838 | ||||||
| chr17:44447074
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.194-10529C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447074 | ||||||
| chr17:44447101
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.194-10556C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447101 | ||||||
| chr17:44447161
|
A | AT | 8 | a0001c0001t0001g0074a0001c0002t0002g0004a0001c0002t0002g0005others(5): Show | 8 | HG02040.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-10617dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447161 | ||||||
| chr17:44447161
|
AT | A | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0040others(17): Show | 20 | HG01975.hp2 HG01978.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.194-10617delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447161 | ||||||
| chr17:44447162
|
T | A | 14 | a0001c0001t0001g0026a0001c0002t0001g0011a0001c0002t0001g0012others(11): Show | 14 | HG01074.hp1 HG01099.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-10617A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447162 | ||||||
| chr17:44447163
|
T | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-10618A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447163 | ||||||
| chr17:44447220
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.194-10675A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447220 | ||||||
| chr17:44447524
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-10979G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447524 | ||||||
| chr17:44447537
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-10992A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447537 | ||||||
| chr17:44447619
|
CT | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0133a0001c0001t0001g0152others(9): Show | 12 | HG01169.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-11075delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447619 | ||||||
| chr17:44447648
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.194-11103A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447648 | ||||||
| chr17:44447662
|
A | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-11117T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447662 | ||||||
| chr17:44447984
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.194-11439G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447984 | ||||||
| chr17:44447993
|
G | A | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.194-11448C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44447993 | ||||||
| chr17:44448292
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-11747A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448292 | ||||||
| chr17:44448359
|
A | G | 1 | a0001c0002t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.194-11814T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448359 | ||||||
| chr17:44448489
|
C | CA | 19 | a0001c0002t0001g0014a0001c0002t0001g0156a0001c0002t0001g0165others(16): Show | 19 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.194-11945dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448489 | ||||||
| chr17:44448489
|
CA | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0086others(3): Show | 6 | HG02145.hp2 HG03239.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-11945delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448489 | ||||||
| chr17:44448503
|
A | AG | 52 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.194-11959dupC | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448503 | ||||||
| chr17:44448503
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0158a0001c0014t0001g0053others(1): Show | 4 | HG01109.hp2 HG01978.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-11958T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448503 | ||||||
| chr17:44448503
|
AG | A | 54 | a0001c0001t0001g0028a0001c0001t0001g0059a0001c0001t0001g0062others(51): Show | 54 | HG00639.hp1 HG00738.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.194-11959delC | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448503 | ||||||
| chr17:44448504
|
G | A | 14 | a0001c0001t0001g0003a0001c0002t0001g0011a0001c0002t0001g0012others(11): Show | 14 | HG02717.hp2 HG02809.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.194-11959C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448504 | ||||||
| chr17:44448505
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-11960C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448505 | ||||||
| chr17:44448506
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.194-11961C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448506 | ||||||
| chr17:44448515
|
GAAGAAGG others(1): Show |
G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG02922.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.194-11978_194-1197 others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448515 | ||||||
| chr17:44448515
|
GAAGAAGG others(4): Show |
G | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.194-11981_194-1197 others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448515 | ||||||
| chr17:44448515
|
GAAGAAGG others(5): Show |
G | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.194-11982_194-1197 others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448515 | ||||||
| chr17:44448521
|
GGAGGAAG others(24): Show |
G | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-12007_194-1197 others(35): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448521 | ||||||
| chr17:44448525
|
GAA | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG02922.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.194-11982_194-1198 others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448525 | ||||||
| chr17:44448527
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.194-11982T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448527 | ||||||
| chr17:44448529
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-11984T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448529 | ||||||
| chr17:44448535
|
A | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01243.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-11990T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448535 | ||||||
| chr17:44448535
|
AAGGAAGA others(11): Show |
A | 5 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0157others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-12008_194-1199 others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448535 | ||||||
| chr17:44448537
|
GGAAGAA | G | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.194-11998_194-1199 others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448537 | ||||||
| chr17:44448548
|
AGGAAG | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG01243.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-12008_194-1200 others(9): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448548 | ||||||
| chr17:44448558
|
AGAAGAAG others(8): Show |
A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-12028_194-1201 others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448558 | ||||||
| chr17:44448573
|
GGAA | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0089others(5): Show | 8 | HG02055.hp1 HG02723.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-12031_194-1202 others(7): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448573 | ||||||
| chr17:44448573
|
GGAAGAA | G | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.194-12034_194-1202 others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448573 | ||||||
| chr17:44448718
|
C | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-12173G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448718 | ||||||
| chr17:44448758
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194-12213T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448758 | ||||||
| chr17:44448767
|
C | T | 8 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(5): Show | 8 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-12222G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448767 | ||||||
| chr17:44448776
|
T | TA | 10 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(7): Show | 10 | HG00323.hp1 HG01106.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-12232dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448776 | ||||||
| chr17:44448776
|
TA | T | 10 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(7): Show | 10 | HG01243.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-12232delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448776 | ||||||
| chr17:44448786
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.194-12241T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448786 | ||||||
| chr17:44448790
|
T | A | 8 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(5): Show | 8 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-12245A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448790 | ||||||
| chr17:44448857
|
A | G | 1 | a0001c0002t0001g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.194-12312T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44448857 | ||||||
| chr17:44449047
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.194-12502C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449047 | ||||||
| chr17:44449060
|
T | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.194-12515A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449060 | ||||||
| chr17:44449221
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.194-12676C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449221 | ||||||
| chr17:44449231
|
C | T | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.194-12686G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449231 | ||||||
| chr17:44449272
|
T | C | 6 | a0001c0002t0001g0198a0001c0002t0001g0216a0001c0002t0001g0251others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-12727A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449272 | ||||||
| chr17:44449513
|
C | CT | 27 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0042others(24): Show | 27 | HG00408.hp1 HG00621.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.194-12969dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449513 | ||||||
| chr17:44449531
|
C | A | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194-12986G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449531 | ||||||
| chr17:44449554
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.194-13009A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449554 | ||||||
| chr17:44449602
|
C | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.194-13057G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449602 | ||||||
| chr17:44449756
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.194-13211C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449756 | ||||||
| chr17:44449987
|
T | A | 2 | a0001c0002t0001g0320a0001c0002t0001g0321 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.194-13442A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44449987 | ||||||
| chr17:44450081
|
G | A | 1 | a0001c0004t0001g0218 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.194-13536C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44450081 | ||||||
| chr17:44450560
|
T | C | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+13912A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44450560 | ||||||
| chr17:44450585
|
A | AAAGATAT others(1): Show |
179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+13886_193+1388 others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44450585 | ||||||
| chr17:44450826
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+13646A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44450826 | ||||||
| chr17:44451162
|
C | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.193+13310G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451162 | ||||||
| chr17:44451368
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.193+13104G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451368 | ||||||
| chr17:44451391
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+13081G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451391 | ||||||
| chr17:44451394
|
A | C | 12 | a0001c0003t0001g0144a0001c0003t0001g0166a0001c0003t0001g0174others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.193+13078T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451394 | ||||||
| chr17:44451631
|
A | T | 1 | a0001c0002t0001g0208 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.193+12841T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451631 | ||||||
| chr17:44451655
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.193+12817G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451655 | ||||||
| chr17:44451657
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.193+12815T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451657 | ||||||
| chr17:44451719
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+12753A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451719 | ||||||
| chr17:44451764
|
C | T | 1 | a0001c0002t0001g0290 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.193+12708G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451764 | ||||||
| chr17:44451769
|
C | T | 2 | a0001c0002t0001g0221a0001c0002t0001g0231 | 2 | NA18939.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.193+12703G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451769 | ||||||
| chr17:44451971
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+12501C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44451971 | ||||||
| chr17:44452262
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.193+12210G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452262 | ||||||
| chr17:44452272
|
C | CA | 20 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0129others(17): Show | 20 | HG00642.hp2 HG01074.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+12199dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452272 | ||||||
| chr17:44452272
|
CA | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0149others(16): Show | 19 | HG01109.hp2 HG01243.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.193+12199delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452272 | ||||||
| chr17:44452290
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.193+12182C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452290 | ||||||
| chr17:44452291
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+12181T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452291 | ||||||
| chr17:44452297
|
A | G | 3 | a0001c0002t0001g0292a0001c0002t0001g0294a0001c0002t0001g0303 | 3 | HG01243.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.193+12175T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452297 | ||||||
| chr17:44452303
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.193+12169T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452303 | ||||||
| chr17:44452305
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.193+12167C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452305 | ||||||
| chr17:44452709
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.193+11763C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452709 | ||||||
| chr17:44452733
|
T | C | 2 | a0001c0002t0002g0008a0001c0002t0002g0010 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.193+11739A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452733 | ||||||
| chr17:44452827
|
C | CT | 49 | a0001c0001t0001g0003a0001c0002t0001g0156a0001c0002t0001g0165others(46): Show | 49 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.193+11644dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44452827 | ||||||
| chr17:44453179
|
G | C | 1 | a0001c0003t0001g0144 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.193+11293C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453179 | ||||||
| chr17:44453399
|
T | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0094others(1): Show | 4 | HG00408.hp2 NA18965.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+11073A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453399 | ||||||
| chr17:44453490
|
G | GGGGTGTG others(9): Show |
1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+10981_193+1098 others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(3): Show |
3 | a0001c0002t0001g0216a0001c0002t0001g0266a0001c0002t0001g0298 | 3 | HG03942.hp2 NA18906.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.193+10981_193+1098 others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(5): Show |
2 | a0001c0002t0001g0261a0001c0002t0001g0304 | 2 | HG00741.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.193+10981_193+1098 others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(7): Show |
1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+10981_193+1098 others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(11): Show |
1 | a0001c0002t0001g0262 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.193+10981_193+1098 others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(17): Show |
1 | a0001c0002t0001g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193+10981_193+1098 others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453490
|
G | GGTGTGTG others(19): Show |
1 | a0001c0002t0014g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.193+10981_193+1098 others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453490 | ||||||
| chr17:44453493
|
A | G | 11 | a0001c0002t0001g0198a0001c0002t0001g0216a0001c0002t0001g0251others(8): Show | 11 | HG00099.hp2 HG00741.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+10979T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453493 | ||||||
| chr17:44453494
|
G | GGT | 6 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+10976_193+1097 others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(1): Show |
13 | a0001c0002t0001g0012a0001c0002t0001g0014a0001c0002t0001g0165others(10): Show | 13 | HG01106.hp1 HG01257.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(3): Show |
19 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0017others(16): Show | 19 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(5): Show |
15 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0156others(12): Show | 15 | HG00642.hp2 HG01099.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(7): Show |
16 | a0001c0002t0001g0013a0001c0002t0001g0167a0001c0002t0001g0206others(13): Show | 16 | HG00673.hp1 HG01081.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(9): Show |
11 | a0001c0002t0001g0208a0001c0002t0001g0212a0001c0002t0001g0228others(8): Show | 11 | HG00621.hp1 HG01074.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(11): Show |
11 | a0001c0002t0001g0231a0001c0002t0001g0236a0001c0002t0001g0241others(8): Show | 11 | HG01496.hp1 HG02040.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(13): Show |
14 | a0001c0002t0001g0211a0001c0002t0001g0214a0001c0002t0001g0221others(11): Show | 14 | HG00438.hp1 HG01069.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(15): Show |
11 | a0001c0002t0001g0205a0001c0002t0001g0210a0001c0002t0001g0224others(8): Show | 11 | HG00642.hp1 HG01261.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(17): Show |
12 | a0001c0002t0001g0203a0001c0002t0001g0225a0001c0002t0001g0226others(9): Show | 12 | HG00408.hp1 HG01243.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(19): Show |
5 | a0001c0002t0001g0252a0001c0002t0001g0255a0001c0002t0001g0260others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(21): Show |
7 | a0001c0002t0001g0215a0001c0002t0001g0222a0001c0002t0001g0235others(4): Show | 7 | HG01106.hp2 HG02004.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+10977_193+1097 others(32): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(23): Show |
1 | a0001c0002t0001g0288 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.193+10977_193+1097 others(34): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(25): Show |
2 | a0001c0002t0001g0271a0001c0004t0001g0223 | 2 | HG00423.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.193+10977_193+1097 others(36): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | GGTGTGTG others(27): Show |
1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.193+10977_193+1097 others(38): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453494
|
G | T | 11 | a0001c0002t0001g0198a0001c0002t0001g0216a0001c0002t0001g0251others(8): Show | 11 | HG00099.hp2 HG00741.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+10978C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453494 | ||||||
| chr17:44453497
|
A | G | 160 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(157): Show | 160 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.193+10975T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453497 | ||||||
| chr17:44453498
|
G | GGTGTGTG others(17): Show |
1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193+10973_193+1097 others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453498 | ||||||
| chr17:44453498
|
G | GTGTGTGT others(14): Show |
1 | a0001c0002t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193+10973_193+1097 others(25): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453498 | ||||||
| chr17:44453498
|
G | T | 160 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(157): Show | 160 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.193+10974C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453498 | ||||||
| chr17:44453500
|
G | GGT | 24 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0032others(21): Show | 24 | HG00280.hp1 HG00280.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.193+10970_193+1097 others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGT | 5 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0079others(2): Show | 5 | HG01109.hp1 HG01358.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+10968_193+1097 others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(19): Show |
1 | a0001c0001t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193+10946_193+1097 others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(21): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.193+10944_193+1097 others(32): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(23): Show |
1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+10942_193+1097 others(34): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(25): Show |
1 | a0001c0001t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193+10971_193+1097 others(36): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(27): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.193+10971_193+1097 others(38): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(29): Show |
1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.193+10971_193+1097 others(40): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(31): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0161 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.193+10971_193+1097 others(42): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(33): Show |
1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193+10971_193+1097 others(44): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(37): Show |
1 | a0001c0001t0001g0162 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193+10971_193+1097 others(48): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | GGTGTGTG others(39): Show |
3 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02145.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.193+10971_193+1097 others(50): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453500
|
G | T | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.193+10972C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453500 | ||||||
| chr17:44453502
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0324 | 2 | HG02083.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.193+10970A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453502 | ||||||
| chr17:44453528
|
T | TGTGTGCG others(3): Show |
1 | a0001c0002t0001g0293 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.193+10943_193+1094 others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453528 | ||||||
| chr17:44453530
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+10942A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453530 | ||||||
| chr17:44453530
|
T | TGTGTGTG others(7): Show |
1 | a0001c0002t0010g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.193+10941_193+1094 others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453530 | ||||||
| chr17:44453541
|
G | A | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.193+10931C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453541 | ||||||
| chr17:44453931
|
CA | C | 145 | a0001c0001t0001g0028a0001c0002t0001g0002a0001c0002t0001g0156others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.193+10540delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453931 | ||||||
| chr17:44453953
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193+10519A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453953 | ||||||
| chr17:44453998
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+10474T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44453998 | ||||||
| chr17:44454162
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+10310C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454162 | ||||||
| chr17:44454250
|
C | T | 14 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 14 | HG01975.hp2 HG01978.hp1 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+10222G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454250 | ||||||
| chr17:44454580
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.193+9892G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454580 | ||||||
| chr17:44454718
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.193+9754G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454718 | ||||||
| chr17:44454761
|
A | ACCTTAGA others(4): Show |
1 | a0001c0001t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.193+9700_193+9710d others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454761 | ||||||
| chr17:44454762
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193+9710G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44454762 | ||||||
| chr17:44455128
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.193+9344A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455128 | ||||||
| chr17:44455192
|
T | C | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.193+9280A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455192 | ||||||
| chr17:44455375
|
C | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.193+9097G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455375 | ||||||
| chr17:44455393
|
C | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.193+9079G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455393 | ||||||
| chr17:44455417
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193+9055G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455417 | ||||||
| chr17:44455840
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.193+8632A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455840 | ||||||
| chr17:44455855
|
C | T | 1 | a0001c0002t0010g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.193+8617G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455855 | ||||||
| chr17:44455943
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.193+8529G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455943 | ||||||
| chr17:44455983
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.193+8489C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44455983 | ||||||
| chr17:44456036
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+8436T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456036 | ||||||
| chr17:44456096
|
TGAGACAG others(20): Show |
T | 17 | a0001c0002t0001g0208a0001c0002t0001g0210a0001c0002t0001g0211others(14): Show | 17 | HG00408.hp1 HG01261.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+8349_193+8375d others(29): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456096 | ||||||
| chr17:44456365
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.193+8107G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456365 | ||||||
| chr17:44456422
|
G | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+8050C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456422 | ||||||
| chr17:44456478
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+7994G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456478 | ||||||
| chr17:44456478
|
CAT | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+7992_193+7993d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456478 | ||||||
| chr17:44456843
|
T | C | 1 | a0001c0002t0001g0280 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193+7629A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456843 | ||||||
| chr17:44456847
|
A | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+7625T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456847 | ||||||
| chr17:44456850
|
G | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+7622C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456850 | ||||||
| chr17:44456869
|
AT | A | 15 | a0001c0001t0001g0133a0001c0001t0001g0183a0001c0001t0001g0184others(12): Show | 15 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+7602delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44456869 | ||||||
| chr17:44457006
|
G | T | 1 | a0001c0002t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.193+7466C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457006 | ||||||
| chr17:44457131
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193+7341C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457131 | ||||||
| chr17:44457152
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.193+7320A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457152 | ||||||
| chr17:44457178
|
T | C | 1 | a0001c0001t0011g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.193+7294A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457178 | ||||||
| chr17:44457239
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0094others(1): Show | 4 | HG00408.hp2 NA18965.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+7233A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457239 | ||||||
| chr17:44457530
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.193+6942G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457530 | ||||||
| chr17:44457883
|
C | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+6589G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457883 | ||||||
| chr17:44457898
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+6574C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44457898 | ||||||
| chr17:44458007
|
C | T | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6465G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458007 | ||||||
| chr17:44458128
|
G | A | 3 | a0001c0002t0001g0204a0001c0002t0001g0209a0001c0002t0001g0233 | 3 | HG01952.hp1 HG02148.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.193+6344C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458128 | ||||||
| chr17:44458133
|
C | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+6339G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458133 | ||||||
| chr17:44458208
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.193+6264C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458208 | ||||||
| chr17:44458255
|
G | GA | 40 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.193+6216dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458255 | ||||||
| chr17:44458273
|
A | AT | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+6198_193+6199i others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458273 | ||||||
| chr17:44458299
|
T | G | 1 | a0001c0002t0001g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.193+6173A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458299 | ||||||
| chr17:44458365
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.193+6107A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458365 | ||||||
| chr17:44458471
|
A | G | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.193+6001T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458471 | ||||||
| chr17:44458647
|
A | G | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG02886.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+5825T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458647 | ||||||
| chr17:44458699
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+5773T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458699 | ||||||
| chr17:44458779
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+5693G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458779 | ||||||
| chr17:44458928
|
A | G | 1 | a0001c0002t0001g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.193+5544T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458928 | ||||||
| chr17:44458933
|
T | G | 1 | a0001c0002t0001g0280 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193+5539A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44458933 | ||||||
| chr17:44459269
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+5203C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44459269 | ||||||
| chr17:44459640
|
G | T | 2 | a0001c0001t0001g0157a0008c0007t0001g0163 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.193+4832C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44459640 | ||||||
| chr17:44459677
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.193+4795T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44459677 | ||||||
| chr17:44459731
|
T | TA | 20 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0036others(17): Show | 20 | HG00621.hp2 HG00738.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+4740dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44459731 | ||||||
| chr17:44460154
|
C | T | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.193+4318G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460154 | ||||||
| chr17:44460232
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.193+4240G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460232 | ||||||
| chr17:44460339
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+4133C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460339 | ||||||
| chr17:44460345
|
T | C | 2 | a0001c0002t0001g0320a0001c0002t0001g0321 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.193+4127A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460345 | ||||||
| chr17:44460359
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193+4113A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460359 | ||||||
| chr17:44460460
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4012G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460460 | ||||||
| chr17:44460685
|
C | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+3787G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460685 | ||||||
| chr17:44460998
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+3474T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44460998 | ||||||
| chr17:44461119
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.193+3353G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461119 | ||||||
| chr17:44461322
|
T | C | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.193+3150A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461322 | ||||||
| chr17:44461393
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.193+3079G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461393 | ||||||
| chr17:44461692
|
T | G | 1 | a0001c0002t0001g0259 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.193+2780A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461692 | ||||||
| chr17:44461708
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.193+2764C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461708 | ||||||
| chr17:44461862
|
TG | T | 144 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.193+2609delC | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44461862 | ||||||
| chr17:44462092
|
C | G | 1 | a0001c0002t0008g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.193+2380G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462092 | ||||||
| chr17:44462109
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.193+2363A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462109 | ||||||
| chr17:44462201
|
C | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+2271G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462201 | ||||||
| chr17:44462297
|
G | C | 2 | a0001c0002t0004g0273a0001c0002t0004g0274 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.193+2175C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462297 | ||||||
| chr17:44462347
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+2125G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462347 | ||||||
| chr17:44462496
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+1976C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462496 | ||||||
| chr17:44462520
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.193+1952C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462520 | ||||||
| chr17:44462710
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.193+1762G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462710 | ||||||
| chr17:44462737
|
C | G | 1 | a0005c0009t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.193+1735G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462737 | ||||||
| chr17:44462749
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+1723C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462749 | ||||||
| chr17:44462798
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+1674G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462798 | ||||||
| chr17:44462906
|
G | A | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.193+1566C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462906 | ||||||
| chr17:44462959
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0125others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+1513G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462959 | ||||||
| chr17:44462968
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.193+1504C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462968 | ||||||
| chr17:44462985
|
T | TATAA | 24 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.193+1483_193+1486d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44462985
|
T | TATAAATA others(1): Show |
9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01192.hp1 HG02074.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+1479_193+1486d others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44462985
|
T | TATAAATA others(5): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.193+1475_193+1486d others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44462985
|
TATAA | T | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.193+1483_193+1486d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44462985
|
TATAAATA others(1): Show |
T | 169 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(166): Show | 169 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.193+1479_193+1486d others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44462985
|
TATAAATA others(5): Show |
T | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+1475_193+1486d others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44462985 | ||||||
| chr17:44463029
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+1443T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463029 | ||||||
| chr17:44463116
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+1356A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463116 | ||||||
| chr17:44463197
|
G | C | 2 | a0001c0002t0001g0227a0001c0002t0001g0243 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.193+1275C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463197 | ||||||
| chr17:44463351
|
C | T | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+1121G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463351 | ||||||
| chr17:44463377
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193+1095C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463377 | ||||||
| chr17:44463384
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.193+1088C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463384 | ||||||
| chr17:44463459
|
T | A | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.193+1013A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463459 | ||||||
| chr17:44463763
|
A | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.193+709T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463763 | ||||||
| chr17:44463971
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+501A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44463971 | ||||||
| chr17:44464007
|
T | G | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+465A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44464007 | ||||||
| chr17:44464160
|
T | C | 1 | a0001c0002t0001g0276 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.193+312A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44464160 | ||||||
| chr17:44464170
|
T | C | 2 | a0001c0002t0001g0314a0001c0002t0001g0315 | 2 | NA18939.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.193+302A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 3/7 | chr17 | 44464170 | ||||||
| chr17:44464837
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-293T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44464837 | ||||||
| chr17:44464933
|
A | AT | 6 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01109.hp2 HG01993.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-390dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44464933 | ||||||
| chr17:44465093
|
A | AAATAAT | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.121-555_121-550dup others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44465093 | ||||||
| chr17:44465325
|
T | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.121-781A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44465325 | ||||||
| chr17:44465782
|
C | T | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.121-1238G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44465782 | ||||||
| chr17:44465996
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-1452A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44465996 | ||||||
| chr17:44466023
|
C | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0094others(1): Show | 4 | HG00408.hp2 NA18965.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-1479G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44466023 | ||||||
| chr17:44466240
|
T | C | 1 | a0001c0002t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.121-1696A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44466240 | ||||||
| chr17:44466337
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.121-1793G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44466337 | ||||||
| chr17:44466455
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121-1911G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44466455 | ||||||
| chr17:44466872
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.121-2328A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44466872 | ||||||
| chr17:44467339
|
G | A | 3 | a0001c0002t0001g0002a0001c0002t0001g0228a0001c0002t0001g0279 | 3 | HG01928.hp1 HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.121-2795C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44467339 | ||||||
| chr17:44467812
|
C | T | 1 | a0001c0002t0001g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.121-3268G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44467812 | ||||||
| chr17:44467825
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-3281C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44467825 | ||||||
| chr17:44468003
|
A | AT | 8 | a0001c0001t0001g0094a0001c0001t0001g0114a0001c0001t0001g0119others(5): Show | 8 | HG00423.hp2 HG00621.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-3460dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468003 | ||||||
| chr17:44468024
|
C | T | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.121-3480G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468024 | ||||||
| chr17:44468184
|
G | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0263 | 2 | HG00408.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.121-3640C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468184 | ||||||
| chr17:44468215
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.121-3671G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468215 | ||||||
| chr17:44468348
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-3804G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468348 | ||||||
| chr17:44468373
|
C | CT | 36 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0043others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-3830dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTT | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0150others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-3831_121-3830d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTT | C | 14 | a0001c0001t0001g0028a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 14 | HG01993.hp1 HG02071.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.121-3835_121-3830d others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(2): Show |
C | 14 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(11): Show | 14 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.121-3838_121-3830d others(11): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0002t0001g0232a0001c0002t0001g0277a0001c0002t0001g0292others(6): Show | 9 | HG01243.hp1 HG02615.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-3839_121-3830d others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(4): Show |
C | 135 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(132): Show | 135 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.121-3840_121-3830d others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0001g0231a0001c0002t0004g0274 | 2 | HG03491.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.121-3841_121-3830d others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0024a0001c0001t0001g0057 | 2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.121-3842_121-3830d others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468373
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0193 | 3 | HG02155.hp2 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.121-3845_121-3830d others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468373 | ||||||
| chr17:44468387
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.121-3843A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468387 | ||||||
| chr17:44468512
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.121-3968G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468512 | ||||||
| chr17:44468593
|
T | A | 1 | a0001c0002t0002g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.121-4049A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468593 | ||||||
| chr17:44468770
|
G | A | 1 | a0001c0001t0016g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.121-4226C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468770 | ||||||
| chr17:44468856
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-4312A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468856 | ||||||
| chr17:44468977
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.121-4433G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468977 | ||||||
| chr17:44468987
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.121-4443A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44468987 | ||||||
| chr17:44469366
|
T | C | 2 | a0001c0002t0001g0308a0001c0002t0001g0309 | 2 | NA18975.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.121-4822A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44469366 | ||||||
| chr17:44469506
|
C | T | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.121-4962G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44469506 | ||||||
| chr17:44469550
|
C | A | 18 | a0001c0002t0001g0212a0001c0002t0001g0220a0001c0002t0001g0266others(15): Show | 18 | HG00438.hp1 HG02132.hp1 NA18612.hp2 others(15): Show |
intron_variant | MODIFIER | c.121-5006G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44469550 | ||||||
| chr17:44469587
|
C | T | 1 | a0001c0002t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.121-5043G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44469587 | ||||||
| chr17:44469619
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.121-5075A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44469619 | ||||||
| chr17:44470040
|
G | A | 5 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(2): Show | 5 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+4789C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470040 | ||||||
| chr17:44470102
|
C | T | 7 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(4): Show | 7 | HG00323.hp1 HG01106.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+4727G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470102 | ||||||
| chr17:44470320
|
C | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.120+4509G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470320 | ||||||
| chr17:44470494
|
C | CT | 75 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0028others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.120+4334dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470494 | ||||||
| chr17:44470494
|
C | CTT | 8 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+4333_120+4334d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470494 | ||||||
| chr17:44470494
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.120+4323_120+4334d others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470494 | ||||||
| chr17:44470604
|
C | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0263 | 2 | HG00408.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.120+4225G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470604 | ||||||
| chr17:44470613
|
C | T | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.120+4216G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470613 | ||||||
| chr17:44470813
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.120+4016A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470813 | ||||||
| chr17:44470844
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.120+3985G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470844 | ||||||
| chr17:44470874
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.120+3955A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44470874 | ||||||
| chr17:44471144
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.120+3685A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44471144 | ||||||
| chr17:44471352
|
C | G | 1 | a0001c0002t0001g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.120+3477G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44471352 | ||||||
| chr17:44471872
|
TA | T | 167 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(164): Show | 167 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.120+2956delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44471872 | ||||||
| chr17:44472112
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.120+2717A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472112 | ||||||
| chr17:44472144
|
A | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.120+2685T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472144 | ||||||
| chr17:44472213
|
T | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2616A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472213 | ||||||
| chr17:44472380
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2449C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472380 | ||||||
| chr17:44472424
|
T | G | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2405A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472424 | ||||||
| chr17:44472512
|
C | T | 125 | a0001c0002t0001g0002a0001c0002t0001g0198a0001c0002t0001g0202others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.120+2317G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472512 | ||||||
| chr17:44472513
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.120+2316C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472513 | ||||||
| chr17:44472624
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.120+2205C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472624 | ||||||
| chr17:44472630
|
C | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.120+2199G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472630 | ||||||
| chr17:44472741
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.120+2088C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472741 | ||||||
| chr17:44472753
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.120+2076A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472753 | ||||||
| chr17:44472852
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.120+1977G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472852 | ||||||
| chr17:44472857
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.120+1972C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44472857 | ||||||
| chr17:44473106
|
A | C | 53 | a0001c0002t0001g0198a0001c0002t0001g0202a0001c0002t0001g0207others(50): Show | 53 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.120+1723T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473106 | ||||||
| chr17:44473135
|
A | AT | 15 | a0001c0001t0001g0032a0001c0001t0001g0058a0001c0001t0001g0094others(12): Show | 15 | HG00621.hp2 HG00741.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+1693dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473135 | ||||||
| chr17:44473229
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+1600C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473229 | ||||||
| chr17:44473235
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.120+1594A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473235 | ||||||
| chr17:44473254
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.120+1575G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473254 | ||||||
| chr17:44473316
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | NA18947.hp1 NA19083.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.120+1513A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473316 | ||||||
| chr17:44473395
|
A | T | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.120+1434T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473395 | ||||||
| chr17:44473486
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.120+1343A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44473486 | ||||||
| chr17:44474066
|
C | T | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.120+763G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44474066 | ||||||
| chr17:44474181
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.120+648C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44474181 | ||||||
| chr17:44474686
|
T | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.120+143A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44474686 | ||||||
| chr17:44474812
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.120+17T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 2/7 | chr17 | 44474812 | ||||||
| chr17:44475189
|
G | C | 1 | a0001c0002t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-286C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475189 | ||||||
| chr17:44475427
|
G | A | 1 | a0008c0007t0001g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46-524C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475427 | ||||||
| chr17:44475464
|
C | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-561G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475464 | ||||||
| chr17:44475787
|
A | C | 8 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0168others(5): Show | 8 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-884T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475787 | ||||||
| chr17:44475862
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-959G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475862 | ||||||
| chr17:44475940
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-1037C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44475940 | ||||||
| chr17:44476029
|
C | CAAACA | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-1131_46-1127dup others(5): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476029 | ||||||
| chr17:44476210
|
C | CCT | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-1308_46-1307ins others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476210 | ||||||
| chr17:44476299
|
G | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-1396C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476299 | ||||||
| chr17:44476387
|
T | A | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-1484A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476387 | ||||||
| chr17:44476420
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-1517C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476420 | ||||||
| chr17:44476846
|
C | A | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.46-1943G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44476846 | ||||||
| chr17:44477232
|
T | C | 162 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0002others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.46-2329A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477232 | ||||||
| chr17:44477307
|
T | G | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-2404A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477307 | ||||||
| chr17:44477424
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.46-2521C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477424 | ||||||
| chr17:44477520
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46-2617G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477520 | ||||||
| chr17:44477522
|
G | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(171): Show | 174 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.46-2619C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477522 | ||||||
| chr17:44477649
|
GA | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-2747delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477649 | ||||||
| chr17:44477717
|
A | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-2814T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477717 | ||||||
| chr17:44477839
|
T | G | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-2936A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477839 | ||||||
| chr17:44477998
|
TGGGGTGG | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-3102_46-3096del others(7): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44477998 | ||||||
| chr17:44478117
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0075others(180): Show | 183 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.46-3214T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478117 | ||||||
| chr17:44478120
|
G | A | 1 | a0001c0002t0001g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-3217C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478120 | ||||||
| chr17:44478258
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.46-3355A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478258 | ||||||
| chr17:44478317
|
A | G | 12 | a0001c0002t0001g0167a0001c0003t0001g0144a0001c0003t0001g0166others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.46-3414T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478317 | ||||||
| chr17:44478419
|
G | A | 150 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0079others(147): Show | 150 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.46-3516C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478419 | ||||||
| chr17:44478532
|
C | T | 1 | a0001c0001t0016g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.46-3629G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478532 | ||||||
| chr17:44478541
|
T | C | 2 | a0001c0002t0001g0320a0001c0002t0001g0321 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.46-3638A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478541 | ||||||
| chr17:44478573
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-3670C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478573 | ||||||
| chr17:44478808
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3905A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478808 | ||||||
| chr17:44478974
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-4071C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44478974 | ||||||
| chr17:44479006
|
T | C | 2 | a0001c0004t0001g0219a0001c0004t0001g0237 | 2 | NA18967.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.46-4103A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479006 | ||||||
| chr17:44479570
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4667T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479570 | ||||||
| chr17:44479596
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.46-4693G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479596 | ||||||
| chr17:44479607
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.46-4704A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479607 | ||||||
| chr17:44479608
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-4705G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479608 | ||||||
| chr17:44479612
|
G | A | 1 | a0001c0003t0001g0181 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.46-4709C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479612 | ||||||
| chr17:44479735
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0104 | 2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.46-4832C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479735 | ||||||
| chr17:44479862
|
G | C | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46-4959C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479862 | ||||||
| chr17:44479926
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-5023G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479926 | ||||||
| chr17:44479965
|
CA | C | 144 | a0001c0001t0001g0033a0001c0001t0001g0107a0001c0001t0001g0189others(141): Show | 144 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.46-5063delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44479965 | ||||||
| chr17:44480127
|
AC | A | 9 | a0001c0002t0001g0289a0001c0002t0001g0304a0001c0002t0002g0004others(6): Show | 9 | HG02004.hp1 HG02004.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-5225delG | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480127 | ||||||
| chr17:44480190
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(7): Show | 10 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-5287C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480190 | ||||||
| chr17:44480244
|
G | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-5341C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480244 | ||||||
| chr17:44480299
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-5396G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480299 | ||||||
| chr17:44480311
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-5408C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480311 | ||||||
| chr17:44480614
|
GGAGGCTG others(144): Show |
G | 1 | a0001c0002t0001g0262 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.46-5862_46-5712del | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480614 | ||||||
| chr17:44480653
|
G | A | 13 | a0001c0002t0001g0210a0001c0002t0001g0211a0001c0002t0001g0214others(10): Show | 13 | HG01261.hp1 HG01496.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.46-5750C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480653 | ||||||
| chr17:44480675
|
G | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-5772C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480675 | ||||||
| chr17:44480707
|
C | CA | 17 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0050others(14): Show | 17 | HG00423.hp2 HG00438.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.46-5805dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480707 | ||||||
| chr17:44480709
|
A | G | 1 | a0001c0004t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.46-5806T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480709 | ||||||
| chr17:44480870
|
T | TCAAAAA | 16 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-5973_46-5968dup others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480870 | ||||||
| chr17:44480890
|
A | G | 5 | a0001c0002t0001g0319a0001c0002t0001g0320a0001c0002t0001g0321others(2): Show | 5 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-5987T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480890 | ||||||
| chr17:44480984
|
C | T | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-6081G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44480984 | ||||||
| chr17:44481186
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-6283G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481186 | ||||||
| chr17:44481189
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.46-6286C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481189 | ||||||
| chr17:44481387
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-6484C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481387 | ||||||
| chr17:44481469
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.46-6566T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481469 | ||||||
| chr17:44481610
|
T | G | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-6707A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481610 | ||||||
| chr17:44481837
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-6934G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481837 | ||||||
| chr17:44481957
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.46-7054C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44481957 | ||||||
| chr17:44482077
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.46-7174G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482077 | ||||||
| chr17:44482145
|
C | T | 12 | a0001c0002t0001g0167a0001c0003t0001g0144a0001c0003t0001g0166others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.46-7242G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482145 | ||||||
| chr17:44482443
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-7540C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482443 | ||||||
| chr17:44482473
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46-7570A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482473 | ||||||
| chr17:44482479
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.46-7576G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482479 | ||||||
| chr17:44482573
|
CA | C | 208 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0024others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.46-7671delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482573 | ||||||
| chr17:44482636
|
CCATGGTA others(20): Show |
C | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.46-7760_46-7734del others(27): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482636 | ||||||
| chr17:44482841
|
G | A | 125 | a0001c0002t0001g0002a0001c0002t0001g0198a0001c0002t0001g0202others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.46-7938C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482841 | ||||||
| chr17:44482873
|
T | TA | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.46-7971dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482873 | ||||||
| chr17:44482904
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.46-8001G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482904 | ||||||
| chr17:44482984
|
G | A | 3 | a0001c0002t0001g0169a0001c0002t0001g0170a0001c0002t0001g0171 | 3 | HG02717.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46-8081C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44482984 | ||||||
| chr17:44483081
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.46-8178T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483081 | ||||||
| chr17:44483154
|
C | CAA | 10 | a0001c0001t0001g0154a0001c0002t0001g0225a0001c0002t0001g0256others(7): Show | 10 | HG00639.hp1 HG01069.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-8253_46-8252dup others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAA | 9 | a0001c0001t0001g0184a0001c0001t0001g0193a0001c0002t0001g0215others(6): Show | 9 | HG01106.hp2 HG01169.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-8254_46-8252dup others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0135others(4): Show | 7 | HG00741.hp1 HG01175.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8260_46-8252dup others(9): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0185a0001c0002t0001g0296a0001c0002t0001g0314others(1): Show | 4 | HG01081.hp2 HG01109.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8261_46-8252dup others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0137 | 3 | HG02074.hp1 HG02083.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.46-8262_46-8252dup others(11): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG01074.hp1 NA18959.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-8263_46-8252dup others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | NA18947.hp1 NA18950.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-8264_46-8252dup others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.46-8266_46-8252dup others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(9): Show |
1 | a0001c0002t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.46-8267_46-8252dup others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0195 | 3 | HG01943.hp1 HG06807.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.46-8269_46-8252dup others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-8270_46-8252dup others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-8271_46-8252dup others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.46-8273_46-8252dup others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46-8252_46-8251ins others(29): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483154
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0065 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46-8252_46-8251ins others(39): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483154 | ||||||
| chr17:44483157
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.46-8283_46-8255del others(29): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483157 | ||||||
| chr17:44483168
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.46-8275_46-8266del others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483168 | ||||||
| chr17:44483170
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.46-8277_46-8268del others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483170 | ||||||
| chr17:44483172
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0140 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.46-8270_46-8269ins others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483172 | ||||||
| chr17:44483173
|
AAAAATAT others(14): Show |
A | 2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.46-8291_46-8271del others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483173 | ||||||
| chr17:44483174
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.46-8271T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483174 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(37): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(44): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(31): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(32): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(27): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0113 | 2 | HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02015.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0018 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(25): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(33): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(14): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0112a0001c0001t0001g0324 | 3 | HG02055.hp2 HG02809.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(11): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0131a0001c0002t0001g0224 | 3 | HG00642.hp1 HG01928.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0036 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(21): Show |
2 | a0001c0002t0001g0243a0001c0003t0001g0175 | 2 | NA19070.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0130a0001c0002t0001g0253a0001c0014t0001g0053 | 3 | HG01978.hp1 HG02630.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(17): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0119 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0003g0019a0001c0002t0001g0277 | 2 | HG00738.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(31): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0002t0001g0310 | 3 | HG00438.hp1 HG00673.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0129 | 2 | HG01975.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(15): Show |
1 | a0001c0003t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(17): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0107a0001c0001t0012g0118others(2): Show | 5 | HG02622.hp2 HG02965.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(19): Show |
5 | a0001c0001t0001g0106a0001c0002t0001g0266a0001c0002t0004g0273others(2): Show | 5 | HG01261.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0174 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(36): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0002t0001g0280 | 3 | NA18941.hp2 NA18982.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(10): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0108others(1): Show | 4 | HG01109.hp1 HG02040.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(17): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(12): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0002t0001g0208others(1): Show | 4 | HG02071.hp2 NA18747.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(14): Show |
2 | a0001c0002t0001g0250a0001c0003t0001g0178 | 2 | HG02083.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
1 | a0001c0002t0001g0270 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(20): Show |
1 | a0001c0002t0001g0212 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(27): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(22): Show |
1 | a0001c0002t0001g0319 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(29): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(28): Show |
1 | a0001c0004t0001g0218 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(35): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(7): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0058others(2): Show | 5 | HG01074.hp2 HG04115.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0001g0149a0001c0002t0001g0202a0001c0003t0001g0181 | 3 | HG00642.hp2 HG02965.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(11): Show |
1 | a0001c0002t0001g0283 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0206a0001c0002t0001g0305 | 2 | HG01168.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(15): Show |
3 | a0001c0002t0001g0244a0001c0002t0001g0245a0001c0002t0001g0269 | 3 | HG04204.hp2 NA18963.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0105a0001c0002t0001g0236 | 2 | HG02040.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(23): Show |
2 | a0001c0002t0001g0303a0001c0002t0001g0307 | 2 | NA18992.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0001g0117a0001c0002t0001g0167 | 2 | HG02071.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(32): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(27): Show |
1 | a0001c0002t0001g0232 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(34): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0001g0078a0001c0003t0001g0176 | 2 | NA18946.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(8): Show |
3 | a0001c0001t0001g0128a0001c0001t0016g0127a0001c0002t0001g0016 | 3 | HG01884.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0072a0001c0002t0001g0207a0002c0005t0001g0054 | 3 | HG01952.hp2 HG04199.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(17): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(14): Show |
3 | a0001c0002t0001g0268a0001c0002t0001g0282a0001c0002t0001g0295 | 3 | NA18942.hp1 NA18952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0116a0001c0002t0001g0302a0006c0011t0001g0201 | 3 | HG04199.hp2 NA18522.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(18): Show |
3 | a0001c0002t0001g0227a0001c0004t0001g0238a0003c0006t0001g0239 | 3 | HG01496.hp1 HG03654.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(25): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(20): Show |
1 | a0004c0015t0001g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(27): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(37): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(34): Show |
1 | a0001c0002t0001g0210 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(41): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0033 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0062a0001c0002t0001g0313a0001c0003t0001g0144others(1): Show | 4 | HG02735.hp2 HG03654.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(9): Show |
2 | a0001c0002t0001g0168a0001c0002t0001g0251 | 2 | HG00323.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(11): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0002t0001g0248others(1): Show | 4 | HG00280.hp2 HG02015.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(13): Show |
1 | a0002c0005t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(15): Show |
3 | a0001c0001t0011g0023a0001c0002t0001g0241a0001c0002t0001g0265 | 3 | HG02145.hp1 NA18951.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0070a0001c0002t0001g0315a0001c0004t0001g0237 | 3 | NA18612.hp1 NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(19): Show |
1 | a0001c0002t0001g0298 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(21): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0002t0001g0211others(1): Show | 4 | HG00423.hp2 HG03942.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(28): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(30): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(34): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(29): Show |
1 | a0001c0002t0001g0306 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(36): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(10): Show |
2 | a0001c0002t0001g0247a0002c0005t0001g0035 | 2 | HG01099.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(17): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(14): Show |
3 | a0001c0002t0001g0275a0001c0002t0010g0217a0001c0004t0001g0223 | 3 | HG00423.hp1 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
5 | a0001c0001t0001g0069a0001c0002t0001g0284a0001c0002t0001g0311others(2): Show | 5 | HG01069.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0290 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(25): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0104 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(27): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(30): Show |
1 | a0001c0002t0001g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(37): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(32): Show |
1 | a0001c0004t0001g0219 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(39): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0002t0001g0015 | 3 | HG02523.hp1 HG02809.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(7): Show |
3 | a0001c0002t0001g0017a0001c0002t0001g0294a0001c0002t0001g0309 | 3 | HG01243.hp1 HG03041.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(9): Show |
2 | a0001c0002t0001g0014a0001c0002t0001g0321 | 2 | HG01168.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(11): Show |
5 | a0001c0002t0001g0267a0001c0002t0001g0308a0001c0002t0001g0320others(2): Show | 5 | HG01169.hp2 HG01358.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(20): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(15): Show |
1 | a0001c0002t0009g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0068a0001c0002t0001g0234a0001c0002t0001g0235 | 3 | HG00621.hp1 HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(19): Show |
2 | a0001c0002t0001g0221a0001c0004t0001g0285 | 2 | NA18965.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(32): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(33): Show |
1 | a0001c0002t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(40): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(11): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(12): Show |
1 | a0001c0002t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(16): Show |
2 | a0001c0002t0001g0171a0001c0002t0001g0205 | 2 | HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.46-8274_46-8273ins others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(25): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(22): Show |
1 | a0001c0002t0001g0231 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(29): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(3): Show |
1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAAAA others(17): Show |
1 | a0001c0002t0001g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(24): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAAAATAT others(12): Show |
1 | a0001c0002t0001g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AAATATAT others(12): Show |
1 | a0001c0002t0001g0233 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-8274_46-8273ins others(19): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.46-8289_46-8274dup others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AATATATA others(11): Show |
1 | a0001c0002t0001g0214 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.46-8291_46-8274dup others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AATATATA others(15): Show |
1 | a0001c0002t0001g0230 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.46-8295_46-8274dup others(22): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.46-8299_46-8274dup others(26): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
A | T | 2 | a0001c0001t0001g0140a0001c0001t0015g0141 | 2 | HG01993.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.46-8273T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AAT | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG01255.hp1 HG01496.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-8275_46-8274del others(2): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(1): Show |
A | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0111others(5): Show | 8 | HG01943.hp2 HG01975.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-8281_46-8274del others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(3): Show |
A | 1 | a0001c0002t0002g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.46-8283_46-8274del others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(5): Show |
A | 6 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-8285_46-8274del others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(7): Show |
A | 1 | a0001c0002t0001g0222 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.46-8287_46-8274del others(14): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(9): Show |
A | 1 | a0001c0002t0001g0264 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.46-8289_46-8274del others(16): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483176
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.46-8291_46-8274del others(18): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483176 | ||||||
| chr17:44483177
|
AT | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0101others(3): Show | 6 | HG00408.hp2 HG00741.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8275delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 7 | HG01081.hp1 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-8281_46-8275del others(7): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(2): Show |
A | 3 | a0001c0001t0001g0099a0001c0002t0001g0316a0005c0009t0001g0143 | 3 | HG02922.hp1 NA18612.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.46-8283_46-8275del others(9): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(4): Show |
A | 2 | a0001c0002t0001g0209a0001c0003t0001g0180 | 2 | HG02148.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.46-8285_46-8275del others(11): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.46-8287_46-8275del others(13): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-8289_46-8275del others(15): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0001g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.46-8291_46-8275del others(17): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(14): Show |
A | 1 | a0001c0002t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-8295_46-8275del others(21): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483177
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.46-8297_46-8275del others(23): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483177 | ||||||
| chr17:44483178
|
T | A | 59 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0031others(56): Show | 59 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.46-8275A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483178 | ||||||
| chr17:44483180
|
T | A | 51 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0032others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.46-8277A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483180 | ||||||
| chr17:44483182
|
T | A | 41 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0064others(38): Show | 41 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.46-8279A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483182 | ||||||
| chr17:44483182
|
T | C | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46-8279A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483182 | ||||||
| chr17:44483184
|
T | A | 34 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0064others(31): Show | 34 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.46-8281A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483184 | ||||||
| chr17:44483186
|
T | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0064others(35): Show | 39 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.46-8283A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483186 | ||||||
| chr17:44483188
|
T | A | 26 | a0001c0001t0001g0064a0001c0001t0001g0098a0001c0001t0001g0099others(23): Show | 26 | HG00099.hp2 HG00408.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.46-8285A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483188 | ||||||
| chr17:44483190
|
T | A | 23 | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0001g0183others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.46-8287A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483190 | ||||||
| chr17:44483192
|
T | A | 14 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0184others(11): Show | 14 | HG00408.hp1 HG01358.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-8289A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483192 | ||||||
| chr17:44483194
|
T | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0148a0001c0001t0001g0193others(3): Show | 6 | HG02155.hp2 HG03239.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-8291A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483194 | ||||||
| chr17:44483196
|
T | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0099a0001c0001t0001g0148others(5): Show | 8 | HG02132.hp2 HG02155.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-8293A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483196 | ||||||
| chr17:44483198
|
T | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0099a0001c0002t0001g0222others(3): Show | 6 | HG02132.hp2 HG03239.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8295A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483198 | ||||||
| chr17:44483200
|
T | A | 6 | a0001c0001t0001g0051a0001c0002t0001g0222a0001c0002t0001g0226others(3): Show | 6 | HG02132.hp2 HG03239.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8297A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483200 | ||||||
| chr17:44483202
|
T | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0100a0001c0002t0001g0264others(1): Show | 4 | HG03239.hp2 NA18944.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-8299A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483202 | ||||||
| chr17:44483204
|
T | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0100a0001c0002t0001g0292 | 3 | NA18944.hp2 NA18966.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.46-8301A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483204 | ||||||
| chr17:44483206
|
T | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0100 | 2 | NA18944.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.46-8303A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483206 | ||||||
| chr17:44483206
|
T | TACACAC | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8304_46-8303ins others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483206 | ||||||
| chr17:44483208
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.46-8305A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483208 | ||||||
| chr17:44483209
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8306T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483209 | ||||||
| chr17:44483212
|
T | C | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-8309A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483212 | ||||||
| chr17:44483214
|
T | C | 10 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0210others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-8311A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483214 | ||||||
| chr17:44483216
|
T | C | 18 | a0001c0002t0001g0212a0001c0002t0001g0220a0001c0002t0001g0266others(15): Show | 18 | HG00438.hp1 HG02132.hp1 HG03195.hp1 others(15): Show |
intron_variant | MODIFIER | c.46-8313A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483216 | ||||||
| chr17:44483337
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-8434C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483337 | ||||||
| chr17:44483419
|
T | A | 137 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.46-8516A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483419 | ||||||
| chr17:44483437
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.46-8534C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483437 | ||||||
| chr17:44483539
|
G | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-8636C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483539 | ||||||
| chr17:44483542
|
A | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.46-8639T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483542 | ||||||
| chr17:44483641
|
CTTTA | C | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8742_46-8739del others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483641 | ||||||
| chr17:44483721
|
A | C | 2 | a0001c0002t0001g0320a0001c0002t0001g0321 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.46-8818T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483721 | ||||||
| chr17:44483729
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-8826G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483729 | ||||||
| chr17:44483784
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.46-8881T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483784 | ||||||
| chr17:44483822
|
G | GTTT | 4 | a0001c0002t0001g0002a0001c0002t0001g0203a0001c0002t0001g0228others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-8922_46-8920dup others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483822 | ||||||
| chr17:44483825
|
T | TTTG | 134 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0011others(131): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.46-8925_46-8923dup others(3): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483825
|
T | TTTGTTG | 6 | a0001c0002t0001g0296a0001c0002t0002g0009a0001c0003t0001g0174others(3): Show | 6 | HG01081.hp2 HG02615.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8928_46-8923dup others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483825
|
T | TTTGTTGT others(2): Show |
10 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0003t0001g0144others(7): Show | 10 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-8931_46-8923dup others(9): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483825
|
T | TTTGTTGT others(5): Show |
7 | a0001c0002t0001g0156a0001c0002t0001g0165a0001c0002t0001g0169others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-8934_46-8923dup others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483825
|
TTTGTTG | T | 4 | a0001c0001t0001g0066a0001c0002t0001g0320a0001c0002t0001g0321others(1): Show | 4 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-8928_46-8923del others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483825
|
TTTGTTGT others(5): Show |
T | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.46-8934_46-8923del others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483825 | ||||||
| chr17:44483902
|
C | T | 2 | a0001c0002t0001g0271a0001c0002t0001g0296 | 2 | HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.46-8999G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483902 | ||||||
| chr17:44483923
|
C | G | 15 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 15 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.46-9020G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483923 | ||||||
| chr17:44483961
|
C | T | 12 | a0001c0002t0001g0167a0001c0003t0001g0144a0001c0003t0001g0166others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.46-9058G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483961 | ||||||
| chr17:44483967
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0001g0291a0001c0002t0006g0272 | 3 | HG01169.hp1 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.46-9064C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483967 | ||||||
| chr17:44483982
|
T | C | 1 | a0001c0002t0001g0276 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-9079A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44483982 | ||||||
| chr17:44484157
|
A | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-9254T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44484157 | ||||||
| chr17:44484555
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.46-9652T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44484555 | ||||||
| chr17:44485119
|
T | A | 1 | a0001c0002t0001g0294 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46-10216A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485119 | ||||||
| chr17:44485260
|
C | A | 1 | a0004c0015t0001g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46-10357G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485260 | ||||||
| chr17:44485260
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-10357G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485260 | ||||||
| chr17:44485264
|
C | T | 161 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(158): Show | 161 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.46-10361G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485264 | ||||||
| chr17:44485281
|
T | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG01243.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-10378A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485281 | ||||||
| chr17:44485287
|
T | A | 1 | a0001c0002t0001g0309 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.46-10384A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485287 | ||||||
| chr17:44485405
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46-10502G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485405 | ||||||
| chr17:44485503
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.46-10600A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485503 | ||||||
| chr17:44485504
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-10601C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485504 | ||||||
| chr17:44485945
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-11042C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44485945 | ||||||
| chr17:44486194
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46-11291A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486194 | ||||||
| chr17:44486268
|
T | A | 1 | a0001c0002t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.46-11365A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486268 | ||||||
| chr17:44486486
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.46-11583T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486486 | ||||||
| chr17:44486507
|
A | T | 1 | a0001c0002t0001g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.46-11604T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486507 | ||||||
| chr17:44486572
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.46-11669C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486572 | ||||||
| chr17:44486604
|
T | C | 2 | a0001c0002t0004g0273a0001c0002t0004g0274 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.46-11701A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44486604 | ||||||
| chr17:44487025
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-12122A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487025 | ||||||
| chr17:44487028
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-12125A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487028 | ||||||
| chr17:44487382
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-12479C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487382 | ||||||
| chr17:44487650
|
C | T | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.46-12747G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487650 | ||||||
| chr17:44487722
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-12819C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487722 | ||||||
| chr17:44487922
|
C | CT | 19 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0065others(16): Show | 19 | HG01175.hp1 HG02300.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-13020dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487922 | ||||||
| chr17:44487961
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.46-13058A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44487961 | ||||||
| chr17:44488004
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0186 | 3 | HG00280.hp1 HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.46-13101G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488004 | ||||||
| chr17:44488033
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.46-13130G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488033 | ||||||
| chr17:44488033
|
CT | C | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-13131delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488033 | ||||||
| chr17:44488082
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.46-13179G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488082 | ||||||
| chr17:44488218
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-13315A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488218 | ||||||
| chr17:44488222
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-13319G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488222 | ||||||
| chr17:44488223
|
C | CT | 148 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0052others(145): Show | 148 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.46-13321dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488223 | ||||||
| chr17:44488223
|
C | CTT | 8 | a0001c0001t0001g0157a0001c0002t0001g0213a0001c0002t0001g0222others(5): Show | 8 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-13322_46-13321d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488223 | ||||||
| chr17:44488223
|
CT | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0110others(4): Show | 7 | HG00408.hp2 HG02922.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-13321delA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488223 | ||||||
| chr17:44488287
|
C | T | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-13384G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488287 | ||||||
| chr17:44488288
|
G | A | 28 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.46-13385C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488288 | ||||||
| chr17:44488419
|
C | A | 1 | a0001c0002t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46-13516G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488419 | ||||||
| chr17:44488517
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46-13614C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488517 | ||||||
| chr17:44488526
|
A | G | 1 | a0004c0015t0001g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46-13623T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488526 | ||||||
| chr17:44488609
|
G | C | 2 | a0001c0003t0001g0179a0001c0003t0001g0181 | 2 | HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.46-13706C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488609 | ||||||
| chr17:44488639
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.46-13736C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488639 | ||||||
| chr17:44488648
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-13745C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488648 | ||||||
| chr17:44488755
|
T | C | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13852A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488755 | ||||||
| chr17:44488756
|
T | G | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13853A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488756 | ||||||
| chr17:44488766
|
C | A | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13863G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488766 | ||||||
| chr17:44488771
|
A | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13868T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488771 | ||||||
| chr17:44488777
|
A | C | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13874T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488777 | ||||||
| chr17:44488779
|
A | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13876T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488779 | ||||||
| chr17:44488781
|
T | A | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13878A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488781 | ||||||
| chr17:44488800
|
A | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13897T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488800 | ||||||
| chr17:44488802
|
A | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13899T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488802 | ||||||
| chr17:44488810
|
G | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13907C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488810 | ||||||
| chr17:44488813
|
A | T | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13910T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488813 | ||||||
| chr17:44488851
|
C | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-13948G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488851 | ||||||
| chr17:44488885
|
A | G | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13982T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488885 | ||||||
| chr17:44488886
|
T | A | 1 | a0001c0003t0001g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-13983A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44488886 | ||||||
| chr17:44489012
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.46-14109A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489012 | ||||||
| chr17:44489263
|
T | C | 1 | a0001c0002t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.45+14063A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489263 | ||||||
| chr17:44489337
|
C | T | 12 | a0001c0002t0001g0167a0001c0003t0001g0144a0001c0003t0001g0166others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+13989G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489337 | ||||||
| chr17:44489389
|
G | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+13937C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489389 | ||||||
| chr17:44489504
|
C | T | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.45+13822G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489504 | ||||||
| chr17:44489556
|
T | A | 15 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 15 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+13770A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489556 | ||||||
| chr17:44489708
|
AC | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+13617delG | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489708 | ||||||
| chr17:44489729
|
T | C | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.45+13597A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489729 | ||||||
| chr17:44489753
|
T | C | 2 | a0001c0003t0001g0179a0001c0003t0001g0181 | 2 | HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.45+13573A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489753 | ||||||
| chr17:44489871
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0197 | 2 | NA18973.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.45+13455C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489871 | ||||||
| chr17:44489982
|
A | G | 7 | a0001c0002t0001g0311a0001c0002t0001g0312a0001c0002t0001g0319others(4): Show | 7 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+13344T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44489982 | ||||||
| chr17:44490023
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.45+13303G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490023 | ||||||
| chr17:44490080
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+13246A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490080 | ||||||
| chr17:44490085
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.45+13241G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490085 | ||||||
| chr17:44490100
|
C | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.45+13226G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490100 | ||||||
| chr17:44490214
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.45+13112C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490214 | ||||||
| chr17:44490504
|
T | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+12822A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490504 | ||||||
| chr17:44490645
|
T | C | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.45+12681A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490645 | ||||||
| chr17:44490654
|
T | TA | 38 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0103others(35): Show | 38 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.45+12671dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490654 | ||||||
| chr17:44490786
|
A | G | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+12540T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44490786 | ||||||
| chr17:44491139
|
T | C | 1 | a0001c0002t0009g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.45+12187A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491139 | ||||||
| chr17:44491300
|
C | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0125 | 3 | HG02622.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.45+12026G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491300 | ||||||
| chr17:44491402
|
G | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(175): Show | 178 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.45+11924C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491402 | ||||||
| chr17:44491470
|
G | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+11856C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491470 | ||||||
| chr17:44491473
|
C | T | 29 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.45+11853G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491473 | ||||||
| chr17:44491486
|
C | CA | 26 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0111others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+11839dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491486 | ||||||
| chr17:44491486
|
CA | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(26): Show | 29 | HG00099.hp1 HG00642.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.45+11839delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491486 | ||||||
| chr17:44491761
|
G | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+11565C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44491761 | ||||||
| chr17:44492161
|
C | T | 2 | a0001c0002t0001g0220a0001c0002t0001g0313 | 2 | NA18971.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.45+11165G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492161 | ||||||
| chr17:44492162
|
G | A | 1 | a0002c0005t0001g0054 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.45+11164C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492162 | ||||||
| chr17:44492233
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+11093C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492233 | ||||||
| chr17:44492297
|
C | CA | 14 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0055others(11): Show | 14 | HG00621.hp2 HG02071.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+11028dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492297 | ||||||
| chr17:44492297
|
C | CAA | 26 | a0001c0001t0001g0162a0001c0002t0001g0011a0001c0002t0001g0012others(23): Show | 26 | HG00323.hp1 HG01106.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+11027_45+11028d others(4): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492297 | ||||||
| chr17:44492297
|
C | CAAA | 120 | a0001c0002t0001g0002a0001c0002t0001g0167a0001c0002t0001g0198others(117): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.45+11026_45+11028d others(5): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492297 | ||||||
| chr17:44492297
|
C | CAAAA | 17 | a0001c0002t0001g0286a0001c0002t0001g0287a0001c0002t0001g0288others(14): Show | 17 | HG00438.hp1 HG00642.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+11025_45+11028d others(6): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492297 | ||||||
| chr17:44492343
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+10983G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492343 | ||||||
| chr17:44492496
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+10830A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492496 | ||||||
| chr17:44492598
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+10728T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492598 | ||||||
| chr17:44492615
|
A | G | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+10711T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492615 | ||||||
| chr17:44492773
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.45+10553C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492773 | ||||||
| chr17:44492860
|
C | T | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10466G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492860 | ||||||
| chr17:44492978
|
G | T | 121 | a0001c0002t0001g0002a0001c0002t0001g0198a0001c0002t0001g0202others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.45+10348C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44492978 | ||||||
| chr17:44493025
|
C | A | 1 | a0007c0016t0001g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.45+10301G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493025 | ||||||
| chr17:44493054
|
G | GT | 6 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(3): Show | 6 | HG02622.hp2 HG03942.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+10271dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493054
|
G | GTTTTTT | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+10266_45+10271d others(8): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493054
|
G | GTTTTTTT | 17 | a0001c0001t0001g0151a0001c0002t0001g0011a0001c0002t0001g0012others(14): Show | 17 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+10265_45+10271d others(9): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493054
|
G | GTTTTTTT others(1): Show |
113 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0154others(110): Show | 113 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.45+10264_45+10271d others(10): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493054
|
G | GTTTTTTT others(2): Show |
38 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0161others(35): Show | 38 | HG00438.hp1 HG00673.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.45+10263_45+10271d others(11): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493054
|
G | GTTTTTTT others(3): Show |
4 | a0001c0001t0001g0160a0001c0002t0001g0306a0001c0002t0001g0313others(1): Show | 4 | HG01433.hp2 HG03130.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+10262_45+10271d others(12): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493054 | ||||||
| chr17:44493145
|
T | C | 1 | a0001c0012t0001g0297 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.45+10181A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493145 | ||||||
| chr17:44493354
|
C | G | 28 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0033others(25): Show | 28 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.45+9972G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493354 | ||||||
| chr17:44493669
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.45+9657A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493669 | ||||||
| chr17:44493736
|
G | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.45+9590C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44493736 | ||||||
| chr17:44494045
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.45+9281C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494045 | ||||||
| chr17:44494118
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+9208G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494118 | ||||||
| chr17:44494310
|
G | T | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+9016C>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494310 | ||||||
| chr17:44494320
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.45+9006C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494320 | ||||||
| chr17:44494409
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.45+8917A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494409 | ||||||
| chr17:44494421
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+8905C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494421 | ||||||
| chr17:44494517
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.45+8809C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494517 | ||||||
| chr17:44494518
|
C | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+8808G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494518 | ||||||
| chr17:44494553
|
T | C | 3 | a0001c0002t0001g0298a0001c0002t0001g0299a0001c0002t0001g0300 | 3 | HG02258.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+8773A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494553 | ||||||
| chr17:44494870
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45+8456A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494870 | ||||||
| chr17:44494931
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.45+8395G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44494931 | ||||||
| chr17:44495026
|
T | C | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+8300A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495026 | ||||||
| chr17:44495089
|
C | A | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.45+8237G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495089 | ||||||
| chr17:44495108
|
G | A | 6 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+8218C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495108 | ||||||
| chr17:44495562
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+7764G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495562 | ||||||
| chr17:44495598
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+7728G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495598 | ||||||
| chr17:44495860
|
T | C | 1 | a0001c0002t0001g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.45+7466A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495860 | ||||||
| chr17:44495872
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+7454A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495872 | ||||||
| chr17:44495875
|
T | G | 1 | a0001c0002t0001g0313 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.45+7451A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495875 | ||||||
| chr17:44495955
|
C | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(4): Show | 7 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+7371G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44495955 | ||||||
| chr17:44496061
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+7265A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44496061 | ||||||
| chr17:44496103
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+7223C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44496103 | ||||||
| chr17:44496159
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0154 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.45+7167G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44496159 | ||||||
| chr17:44496338
|
C | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.45+6988G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44496338 | ||||||
| chr17:44496871
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.45+6455C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44496871 | ||||||
| chr17:44497093
|
C | T | 1 | a0001c0003t0001g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.45+6233G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497093 | ||||||
| chr17:44497208
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+6118T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497208 | ||||||
| chr17:44497221
|
G | A | 1 | a0001c0002t0001g0302 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45+6105C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497221 | ||||||
| chr17:44497388
|
G | C | 1 | a0001c0010t0001g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.45+5938C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497388 | ||||||
| chr17:44497530
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0148others(177): Show | 180 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.45+5796T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497530 | ||||||
| chr17:44497534
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+5792C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497534 | ||||||
| chr17:44497614
|
T | A | 1 | a0001c0002t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+5712A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497614 | ||||||
| chr17:44497777
|
A | G | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+5549T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497777 | ||||||
| chr17:44497839
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.45+5487G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497839 | ||||||
| chr17:44497853
|
T | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+5473A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497853 | ||||||
| chr17:44497900
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+5426G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44497900 | ||||||
| chr17:44498001
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.45+5325G>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498001 | ||||||
| chr17:44498286
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+5040A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498286 | ||||||
| chr17:44498301
|
G | A | 1 | a0001c0002t0001g0304 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.45+5025C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498301 | ||||||
| chr17:44498434
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.45+4892C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498434 | ||||||
| chr17:44498762
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+4564G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498762 | ||||||
| chr17:44498916
|
T | C | 2 | a0001c0002t0001g0306a0001c0002t0001g0307 | 2 | NA18947.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.45+4410A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44498916 | ||||||
| chr17:44499066
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0015g0141 | 2 | HG01993.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.45+4260A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499066 | ||||||
| chr17:44499135
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | HG00738.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.45+4191G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499135 | ||||||
| chr17:44499477
|
T | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0008c0007t0001g0163 | 3 | HG01109.hp2 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.45+3849A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499477 | ||||||
| chr17:44499573
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+3753G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499573 | ||||||
| chr17:44499595
|
G | A | 2 | a0001c0002t0001g0308a0001c0002t0001g0309 | 2 | NA18975.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.45+3731C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499595 | ||||||
| chr17:44499634
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+3692C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499634 | ||||||
| chr17:44499715
|
T | C | 1 | a0001c0002t0001g0310 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.45+3611A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499715 | ||||||
| chr17:44499760
|
A | G | 1 | a0001c0002t0001g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+3566T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499760 | ||||||
| chr17:44499808
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.45+3518A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499808 | ||||||
| chr17:44499897
|
A | AT | 15 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 15 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+3428dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499897 | ||||||
| chr17:44499899
|
T | TA | 10 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0160others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+3426dupT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44499899 | ||||||
| chr17:44500001
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.45+3325T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500001 | ||||||
| chr17:44500099
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.45+3227A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500099 | ||||||
| chr17:44500190
|
G | C | 1 | a0001c0001t0011g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+3136C>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500190 | ||||||
| chr17:44500483
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.45+2843G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500483 | ||||||
| chr17:44500486
|
T | G | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2840A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500486 | ||||||
| chr17:44500727
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.45+2599A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44500727 | ||||||
| chr17:44501215
|
G | A | 1 | a0001c0008t0013g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+2111C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501215 | ||||||
| chr17:44501308
|
T | C | 1 | a0005c0009t0001g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+2018A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501308 | ||||||
| chr17:44501416
|
CA | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.45+1909delT | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501416 | ||||||
| chr17:44501430
|
A | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+1896T>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501430 | ||||||
| chr17:44501514
|
G | A | 162 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.45+1812C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501514 | ||||||
| chr17:44501597
|
T | C | 145 | a0001c0002t0001g0002a0001c0002t0001g0156a0001c0002t0001g0165others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.45+1729A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44501597 | ||||||
| chr17:44502025
|
A | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.45+1301T>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502025 | ||||||
| chr17:44502103
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+1223A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502103 | ||||||
| chr17:44502184
|
T | A | 1 | a0001c0002t0001g0313 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.45+1142A>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502184 | ||||||
| chr17:44502359
|
G | GT | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG00323.hp2 HG00738.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+966dupA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502359 | ||||||
| chr17:44502359
|
GTT | G | 23 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(20): Show | 23 | HG01243.hp2 HG02280.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.45+965_45+966delAA | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502359 | ||||||
| chr17:44502359
|
GTTT | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0001g0158others(151): Show | 154 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.45+964_45+966delAA others(1): Show |
GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502359 | ||||||
| chr17:44502360
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 5 | HG01081.hp1 HG01261.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+966A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502360 | ||||||
| chr17:44502362
|
T | G | 7 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(4): Show | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+964A>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502362 | ||||||
| chr17:44502484
|
C | A | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.45+842G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502484 | ||||||
| chr17:44502510
|
C | T | 15 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(12): Show | 15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+816G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502510 | ||||||
| chr17:44502604
|
T | C | 3 | a0001c0002t0001g0314a0001c0002t0001g0315a0001c0002t0001g0316 | 3 | NA18612.hp2 NA18939.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.45+722A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502604 | ||||||
| chr17:44502636
|
T | C | 15 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 15 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+690A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502636 | ||||||
| chr17:44502693
|
T | C | 125 | a0001c0002t0001g0002a0001c0002t0001g0198a0001c0002t0001g0202others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.45+633A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502693 | ||||||
| chr17:44502711
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+615G>A | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502711 | ||||||
| chr17:44502719
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.45+607C>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502719 | ||||||
| chr17:44502794
|
T | C | 5 | a0001c0002t0001g0319a0001c0002t0001g0320a0001c0002t0001g0321others(2): Show | 5 | HG01069.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+532A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502794 | ||||||
| chr17:44502872
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.45+454T>C | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502872 | ||||||
| chr17:44502988
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.45+338A>G | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44502988 | ||||||
| chr17:44503059
|
C | A | 1 | a0001c0013t0005g0325 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.45+267G>T | GPATCH8 | ENSG00000186566.13 | transcript | ENST00000591680.6 | protein_coding | 1/7 | chr17 | 44503059 |