Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51429 |
|---|---|
| ensemblid | ENSG00000130340.17 |
| hgncid | 14973 |
| symbol | SNX9 |
| name | sorting nexin 9 |
| refseq_nuc | NM_016224.5 |
| refseq_prot | NP_057308.1 |
| ensembl_nuc | ENST00000392185.8 |
| ensembl_prot | ENSP00000376024.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 157823246 |
| end | 157945077 |
| strand | + |
| ver | v1.2 |
| region | chr6:157823246-157945077 |
| region5000 | chr6:157818246-157950077 |
| regionname0 | SNX9_chr6_157823246_157945077 |
| regionname5000 | SNX9_chr6_157818246_157950077 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 595 | 238 | 74 | 37 | 83 | 12 | 30 | 60 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002 | 0/0 | 592 | 57 | 2 | 10 | 36 | 2 | 7 | 25 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0003 | 0/0 | 595 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0004 | 0/0 | 595 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0005 | 0/0 | 595 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0006 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1788 | 200 | 58 | 32 | 77 | 10 | 21 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0002 | 0/0 | 1779 | 55 | 0 | 10 | 36 | 2 | 7 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0003 | 0/0 | 1788 | 29 | 14 | 4 | 1 | 2 | 8 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0004 | 0/0 | 1788 | 4 | 0 | 0 | 4 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0005 | 0/0 | 1788 | 2 | 0 | 1 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0006 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0008 | 0/0 | 1788 | 2 | 0 | 0 | 2 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0009 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0010 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0011 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0012 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0013 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| c0014 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2429 | 178 | 39 | 26 | 80 | 10 | 22 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0002 | 0/0 | 2429 | 52 | 0 | 8 | 36 | 2 | 6 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0003 | 0/1 | 2429 | 34 | 14 | 7 | 1 | 2 | 9 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0004 | 0/0 | 2429 | 7 | 6 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0005 | 0/0 | 2429 | 6 | 6 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0006 | 0/0 | 2429 | 4 | 1 | 0 | 3 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0007 | 0/0 | 2429 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0008 | 0/0 | 2429 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0009 | 0/0 | 2429 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0010 | 0/0 | 2429 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0011 | 0/0 | 2429 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0012 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0013 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0014 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0015 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0016 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0017 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0018 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0019 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0020 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0021 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| t0022 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1788 | 200 | 58 | 32 | 77 | 10 | 21 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0003 | 0/0 | 1788 | 29 | 14 | 4 | 1 | 2 | 8 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0004 | 0/0 | 1788 | 4 | 0 | 0 | 4 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0009 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0010 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0011 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0012 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0013 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0002 | 0/0 | 1779 | 55 | 0 | 10 | 36 | 2 | 7 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0003c0006 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0004c0005 | 0/0 | 1788 | 2 | 0 | 1 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0005c0008 | 0/0 | 1788 | 2 | 0 | 0 | 2 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0006c0014 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4216 | 167 | 36 | 25 | 74 | 10 | 21 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0003 | 0/1 | 4216 | 5 | 2 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0004 | 0/0 | 4216 | 7 | 6 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0005 | 0/0 | 4216 | 5 | 5 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0006 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0009 | 0/0 | 4216 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0010 | 0/0 | 4216 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0011 | 0/0 | 4216 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0013 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0014 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0015 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0016 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0017 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0018 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0019 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0020 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0001t0021 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0003t0003 | 0/0 | 4216 | 27 | 12 | 4 | 1 | 2 | 8 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0003t0005 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0003t0022 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0004t0001 | 0/0 | 4216 | 4 | 0 | 0 | 4 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0009t0006 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0010t0001 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0011t0001 | 0/0 | 4216 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0012t0001 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0001c0013t0001 | 0/0 | 4216 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0002t0002 | 0/0 | 4207 | 52 | 0 | 8 | 36 | 2 | 6 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0002t0008 | 0/0 | 4207 | 2 | 0 | 2 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0002t0012 | 0/0 | 4207 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0002c0007t0007 | 0/0 | 4207 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0003c0006t0001 | 0/0 | 4216 | 2 | 2 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0004c0005t0003 | 0/0 | 4216 | 2 | 0 | 1 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0005c0008t0006 | 0/0 | 4216 | 2 | 0 | 0 | 2 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| a0006c0014t0001 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | copy fasta | chr6 | 157818246 | 157950077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0003g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0016g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0018g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0020g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0001t0021g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0003t0022g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0009t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0010t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0011t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0012t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0001c0013t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0008g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0008g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0002t0012g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0007t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0002c0007t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0003c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0003c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0004c0005t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0004c0005t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0005c0008t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0005c0008t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| a0006c0014t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0286 | EUR | GBR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0044 | EUR | FIN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00544 | hp1 | a0001 | c0001 | t0016 | g0076 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00642 | hp2 | a0004 | c0005 | t0003 | g0283 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0111 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00733 | hp2 | a0002 | c0002 | t0008 | g0024 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00735 | hp1 | a0002 | c0002 | t0008 | g0022 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0279 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0284 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0122 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0281 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0285 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0133 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0045 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01496 | hp1 | a0001 | c0013 | t0001 | g0105 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0132 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0046 | EUR | IBS | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0293 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0266 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0254 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02056 | hp2 | a0001 | c0012 | t0001 | g0202 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02080 | hp1 | a0005 | c0008 | t0006 | g0093 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02135 | hp1 | a0006 | c0014 | t0001 | g0148 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0256 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0252 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02280 | hp1 | a0002 | c0007 | t0007 | g0043 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0271 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0183 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0299 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02723 | hp2 | a0001 | c0009 | t0006 | g0058 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0274 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0263 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0251 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02886 | hp1 | a0001 | c0001 | t0021 | g0291 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0258 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0264 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0287 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0290 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03041 | hp2 | a0001 | c0010 | t0001 | g0059 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03098 | hp1 | a0003 | c0006 | t0001 | g0120 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0265 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03195 | hp1 | a0001 | c0003 | t0022 | g0292 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0064 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0273 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0272 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0060 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03669 | hp2 | a0004 | c0005 | t0003 | g0282 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0276 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03834 | hp2 | a0002 | c0002 | t0012 | g0050 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0203 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03942 | hp2 | a0001 | c0011 | t0001 | g0155 | SAS | BEB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0268 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0269 | SAS | STU | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | YRI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0255 | AFR | YRI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0176 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19001 | hp1 | a0001 | c0001 | t0014 | g0163 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19003 | hp1 | a0005 | c0008 | t0006 | g0074 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0259 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0062 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | YRI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20129 | hp1 | a0002 | c0007 | t0007 | g0054 | AFR | ASW | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0270 | EUR | TSI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0253 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0298 | AFR | ACB | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03471 | hp1 | a0003 | c0006 | t0001 | g0141 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0302 | AFR | USA | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0277 | REF | REF | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | SNX9_chr6_157818246_157950077 | SNX9 | chr6 | 157818246 | 157950077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:157867616
|
A | C | 1 | a0005 | 2 | HG02080.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.82A>C | p.Ile28Leu | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/18 | 271/4216 | 82/1788 | 28/595 | chr6 | 157867616 | ||
| chr6:157875151
|
C | T | 1 | a0006 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.275C>T | p.Ser92Leu | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/18 | 464/4216 | 275/1788 | 92/595 | chr6 | 157875151 | ||
| chr6:157901963
|
G | A | 1 | a0004 | 2 | HG00642.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.538G>A | p.Asp180Asn | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/18 | 727/4216 | 538/1788 | 180/595 | chr6 | 157901963 | ||
| chr6:157942822
|
G | A | 1 | a0003 | 2 | HG03098.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1772G>A | p.Arg591His | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1961/4216 | 1772/1788 | 591/595 | chr6 | 157942822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:157873152
|
G | C | 4 | a0001c0009a0001c0010a0002c0002others(1): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
synonymous_variant | LOW | c.150G>C | p.Gly50Gly | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/18 | 339/4216 | 150/1788 | 50/595 | chr6 | 157873152 | ||
| chr6:157896970
|
C | T | 1 | a0001c0004 | 4 | NA18947.hp2 NA18952.hp1 NA18986.hp2 others(1): Show |
synonymous_variant | LOW | c.444C>T | p.Phe148Phe | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/18 | 633/4216 | 444/1788 | 148/595 | chr6 | 157896970 | ||
| chr6:157901929
|
C | T | 1 | a0001c0013 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.504C>T | p.Asp168Asp | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/18 | 693/4216 | 504/1788 | 168/595 | chr6 | 157901929 | ||
| chr6:157909733
|
G | A | 4 | a0001c0003a0001c0009a0002c0002others(1): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
synonymous_variant | LOW | c.774G>A | p.Arg258Arg | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 8/18 | 963/4216 | 774/1788 | 258/595 | chr6 | 157909733 | ||
| chr6:157927197
|
C | T | 1 | a0001c0012 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.1167C>T | p.Asp389Asp | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/18 | 1356/4216 | 1167/1788 | 389/595 | chr6 | 157927197 | ||
| chr6:157937454
|
C | T | 1 | a0001c0011 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1464C>T | p.Phe488Phe | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/18 | 1653/4216 | 1464/1788 | 488/595 | chr6 | 157937454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:157823268
|
G | T | 4 | a0001c0001t0005a0001c0001t0021a0001c0003t0005others(1): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-167G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/18 | 167 | chr6 | 157823268 | |||||
| chr6:157823330
|
G | A | 4 | a0002c0002t0002a0002c0002t0008a0002c0002t0012others(1): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-105G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/18 | 105 | chr6 | 157823330 | |||||
| chr6:157823330
|
G | T | 1 | a0001c0001t0020 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/18 | 105 | chr6 | 157823330 | |||||
| chr6:157823341
|
C | T | 1 | a0002c0002t0008 | 2 | HG00733.hp2 HG00735.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/18 | chr6 | 157823341 | ||||||
| chr6:157942842
|
A | G | 1 | a0001c0003t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 4 | chr6 | 157942842 | |||||
| chr6:157942863
|
G | A | 1 | a0001c0001t0013 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 25 | chr6 | 157942863 | |||||
| chr6:157942951
|
G | T | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 113 | chr6 | 157942951 | |||||
| chr6:157943041
|
T | A | 1 | a0001c0001t0014 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 203 | chr6 | 157943041 | |||||
| chr6:157943393
|
C | T | 1 | a0001c0001t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 555 | chr6 | 157943393 | |||||
| chr6:157943403
|
G | A | 1 | a0001c0001t0015 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*565G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 565 | chr6 | 157943403 | |||||
| chr6:157943405
|
G | C | 1 | a0001c0001t0014 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 567 | chr6 | 157943405 | |||||
| chr6:157943445
|
G | A | 1 | a0001c0001t0013 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 607 | chr6 | 157943445 | |||||
| chr6:157943682
|
A | G | 8 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(5): Show | 43 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*844A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 844 | chr6 | 157943682 | |||||
| chr6:157943728
|
A | G | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(13): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*890A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 890 | chr6 | 157943728 | |||||
| chr6:157943910
|
A | G | 1 | a0001c0001t0011 | 2 | HG03579.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1072A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1072 | chr6 | 157943910 | |||||
| chr6:157943950
|
C | G | 6 | a0001c0001t0006a0001c0009t0006a0002c0002t0002others(3): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1112C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1112 | chr6 | 157943950 | |||||
| chr6:157944003
|
C | T | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(13): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1165C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1165 | chr6 | 157944003 | |||||
| chr6:157944013
|
C | G | 2 | a0001c0001t0011a0001c0001t0013 | 3 | HG02559.hp2 HG03579.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1175C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1175 | chr6 | 157944013 | |||||
| chr6:157944066
|
A | G | 1 | a0002c0002t0012 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1228 | chr6 | 157944066 | |||||
| chr6:157944138
|
C | T | 4 | a0001c0001t0004a0001c0001t0017a0001c0001t0019others(1): Show | 10 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1300 | chr6 | 157944138 | |||||
| chr6:157944501
|
C | A | 1 | a0001c0001t0013 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1663 | chr6 | 157944501 | |||||
| chr6:157944521
|
G | A | 1 | a0001c0001t0009 | 2 | HG01256.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1683G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1683 | chr6 | 157944521 | |||||
| chr6:157944684
|
G | A | 1 | a0001c0001t0016 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1846 | chr6 | 157944684 | |||||
| chr6:157944740
|
A | G | 1 | a0001c0001t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1902A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 1902 | chr6 | 157944740 | |||||
| chr6:157945050
|
A | C | 1 | a0001c0001t0013 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2212A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 2212 | chr6 | 157945050 | |||||
| chr6:157945051
|
A | G | 1 | a0001c0001t0010 | 2 | HG00733.hp1 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2213A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 18/18 | 2213 | chr6 | 157945051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:157823504
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+58G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823504 | ||||||
| chr6:157823551
|
G | C | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+105G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823551 | ||||||
| chr6:157823691
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+245G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823691 | ||||||
| chr6:157823750
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.12+304C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823750 | ||||||
| chr6:157823781
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+335C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823781 | ||||||
| chr6:157823783
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.12+337C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823783 | ||||||
| chr6:157823818
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+372G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823818 | ||||||
| chr6:157823974
|
G | T | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+528G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157823974 | ||||||
| chr6:157824057
|
C | T | 1 | a0001c0003t0003g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.12+611C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824057 | ||||||
| chr6:157824313
|
C | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+867C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824313 | ||||||
| chr6:157824391
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+945A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824391 | ||||||
| chr6:157824454
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+1008C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824454 | ||||||
| chr6:157824458
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+1012T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824458 | ||||||
| chr6:157824563
|
A | C | 1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+1117A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824563 | ||||||
| chr6:157824721
|
T | C | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+1275T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824721 | ||||||
| chr6:157824787
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+1341A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824787 | ||||||
| chr6:157824891
|
C | G | 1 | a0002c0002t0002g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.12+1445C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824891 | ||||||
| chr6:157824921
|
C | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+1475C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824921 | ||||||
| chr6:157824956
|
T | C | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+1510T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824956 | ||||||
| chr6:157824969
|
C | T | 1 | a0002c0002t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.12+1523C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824969 | ||||||
| chr6:157824982
|
T | C | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+1536T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157824982 | ||||||
| chr6:157825002
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+1556C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825002 | ||||||
| chr6:157825233
|
GCGAGACT others(20): Show |
G | 1 | a0001c0001t0001g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.12+1810_12+1836del others(27): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157825233 | |||||
| chr6:157825319
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+1873G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825319 | ||||||
| chr6:157825411
|
A | G | 115 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0250others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.12+1965A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825411 | ||||||
| chr6:157825448
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.12+2002A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825448 | ||||||
| chr6:157825493
|
C | T | 301 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.12+2047C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825493 | ||||||
| chr6:157825580
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.12+2134A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825580 | ||||||
| chr6:157825622
|
G | A | 9 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0003t0003g0251others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+2176G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825622 | ||||||
| chr6:157825700
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.12+2254G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825700 | ||||||
| chr6:157825954
|
TATAAGTA others(7): Show |
T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+2511_12+2524del others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157825954 | |||||
| chr6:157825972
|
A | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+2526A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157825972 | ||||||
| chr6:157826062
|
T | A | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+2616T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826062 | ||||||
| chr6:157826294
|
C | A | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+2848C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826294 | ||||||
| chr6:157826399
|
C | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+2953C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826399 | ||||||
| chr6:157826495
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3049A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826495 | ||||||
| chr6:157826502
|
GA | G | 24 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(21): Show | 24 | HG01256.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.12+3072delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826502 | |||||
| chr6:157826560
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3114A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826560 | ||||||
| chr6:157826574
|
C | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3128C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826574 | ||||||
| chr6:157826614
|
ACACT | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02145.hp2 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3175_12+3178del others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826614 | |||||
| chr6:157826641
|
TTTTACAA others(119): Show |
T | 15 | a0001c0001t0003g0250a0001c0001t0004g0063a0001c0001t0004g0065others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.12+3196_12+3321del | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826641 | ||||||
| chr6:157826646
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3200C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826646 | ||||||
| chr6:157826657
|
ACAAAAGC others(82): Show |
A | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3212_12+3300del others(89): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826657 | ||||||
| chr6:157826755
|
T | TTA | 57 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+3319_12+3320dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826755 | |||||
| chr6:157826760
|
T | A | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3314T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826760 | ||||||
| chr6:157826760
|
T | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG02083.hp1 NA18966.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+3314T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826760 | ||||||
| chr6:157826761
|
A | G | 2 | a0001c0001t0003g0257a0001c0001t0020g0287 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.12+3315A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826761 | ||||||
| chr6:157826763
|
A | C | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3317A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826763 | ||||||
| chr6:157826765
|
A | T | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3319A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826765 | ||||||
| chr6:157826766
|
T | G | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3320T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826766 | ||||||
| chr6:157826767
|
G | T | 1 | a0001c0001t0003g0257 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+3321G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826767 | ||||||
| chr6:157826771
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3325T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826771 | ||||||
| chr6:157826776
|
ATATAT | A | 22 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0277others(19): Show | 22 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.12+3341_12+3345del others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826776 | |||||
| chr6:157826780
|
AT | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3336delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826780 | |||||
| chr6:157826781
|
T | TTATATTT others(15): Show |
56 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.12+3341_12+3342ins others(22): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826781 | |||||
| chr6:157826781
|
T | TTTTATAT others(1): Show |
3 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.12+3336_12+3337ins others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826781 | |||||
| chr6:157826784
|
TA | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3339delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826784 | ||||||
| chr6:157826788
|
A | T | 216 | a0001c0001t0001g0061a0001c0001t0001g0134a0001c0001t0001g0135others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.12+3342A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826788 | ||||||
| chr6:157826790
|
A | ATATAATA others(53): Show |
1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12+3348_12+3349ins others(60): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826790 | |||||
| chr6:157826791
|
T | C | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3345T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826791 | ||||||
| chr6:157826791
|
T | TTTTATAT others(4): Show |
3 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.12+3345_12+3346ins others(11): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826791 | ||||||
| chr6:157826792
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3346A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826792 | ||||||
| chr6:157826793
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3347T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826793 | ||||||
| chr6:157826793
|
T | TA | 10 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(7): Show | 10 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+3348dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826793 | |||||
| chr6:157826794
|
ATATATTA others(6): Show |
A | 6 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3349_12+3361del others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826794 | ||||||
| chr6:157826799
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3353T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826799 | ||||||
| chr6:157826799
|
T | TA | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3353_12+3354ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826799 | ||||||
| chr6:157826800
|
T | A | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3354T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826800 | ||||||
| chr6:157826805
|
T | A | 9 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3359T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826805 | ||||||
| chr6:157826806
|
T | TG | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3360_12+3361ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826806 | ||||||
| chr6:157826807
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3361T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826807 | ||||||
| chr6:157826811
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3365T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826811 | ||||||
| chr6:157826811
|
TA | T | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3366delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826811 | ||||||
| chr6:157826812
|
A | AT | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3367dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826812 | |||||
| chr6:157826814
|
A | ATATTATA others(8): Show |
1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3368_12+3369ins others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826814 | ||||||
| chr6:157826814
|
A | T | 24 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.12+3368A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826814 | ||||||
| chr6:157826815
|
A | T | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3369A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826815 | ||||||
| chr6:157826815
|
AAT | A | 7 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3376_12+3377del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826815 | |||||
| chr6:157826822
|
AT | A | 17 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+3378delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826822 | |||||
| chr6:157826823
|
T | C | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12+3377T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826823 | ||||||
| chr6:157826824
|
T | A | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3378T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826824 | ||||||
| chr6:157826826
|
TA | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3381delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826826 | ||||||
| chr6:157826829
|
T | A | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3383T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826829 | ||||||
| chr6:157826830
|
T | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3384T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826830 | ||||||
| chr6:157826832
|
A | T | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3386A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826832 | ||||||
| chr6:157826833
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.12+3400_12+3423dup others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826833 | |||||
| chr6:157826833
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0238 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.12+3423_12+3424ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826833 | |||||
| chr6:157826834
|
A | ATATAAAT others(13): Show |
2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3392_12+3393ins others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826834 | |||||
| chr6:157826838
|
AT | A | 7 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(4): Show | 7 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3393delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826838 | ||||||
| chr6:157826841
|
T | A | 7 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(4): Show | 7 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3395T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826841 | ||||||
| chr6:157826841
|
T | TTGTA | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3396_12+3397ins others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826841 | |||||
| chr6:157826842
|
T | A | 2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3396T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826842 | ||||||
| chr6:157826846
|
T | G | 59 | a0001c0001t0001g0134a0001c0001t0009g0132a0001c0001t0009g0133others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+3400T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826846 | ||||||
| chr6:157826846
|
T | TTTTATAT others(17): Show |
4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG00408.hp1 HG00558.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3409_12+3432dup others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826846 | |||||
| chr6:157826846
|
T | TTTTATAT others(59): Show |
4 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3423_12+3424ins others(66): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826846 | |||||
| chr6:157826847
|
T | A | 24 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.12+3401T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826847 | ||||||
| chr6:157826849
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3403T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826849 | ||||||
| chr6:157826849
|
T | TATATA | 54 | a0001c0001t0009g0132a0001c0001t0009g0133a0002c0002t0002g0001others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.12+3404_12+3408dup others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATAAT others(27): Show |
1 | a0001c0001t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+3408_12+3409ins others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATAAT others(489): Show |
3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+3408_12+3409ins others(496): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATAAT others(487): Show |
1 | a0002c0002t0002g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.12+3408_12+3409ins others(494): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATATA others(22): Show |
110 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0071others(107): Show | 110 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.12+3442_12+3470dup others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATATA others(51): Show |
15 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0123others(12): Show | 15 | HG00099.hp1 HG01099.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.12+3413_12+3470dup others(58): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATATA others(46): Show |
1 | a0001c0001t0001g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.12+3432_12+3433ins others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826849
|
T | TATATATA others(16): Show |
1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12+3410_12+3411ins others(23): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826849 | |||||
| chr6:157826850
|
A | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3404A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826850 | ||||||
| chr6:157826853
|
TATAAATA others(135): Show |
T | 1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.12+3408_12+3549del | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826853 | ||||||
| chr6:157826854
|
A | T | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3408A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826854 | ||||||
| chr6:157826855
|
T | A | 38 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(35): Show | 38 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.12+3409T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826855 | ||||||
| chr6:157826855
|
TAAA | T | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3410_12+3412del others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826855 | ||||||
| chr6:157826857
|
A | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3411A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826857 | ||||||
| chr6:157826863
|
T | C | 2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3417T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826863 | ||||||
| chr6:157826864
|
A | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3418A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826864 | ||||||
| chr6:157826865
|
T | C | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3419T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826865 | ||||||
| chr6:157826865
|
T | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3419T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826865 | ||||||
| chr6:157826866
|
T | A | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3420T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826866 | ||||||
| chr6:157826870
|
G | T | 25 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(22): Show | 25 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3424G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826870 | ||||||
| chr6:157826872
|
T | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3426T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826872 | ||||||
| chr6:157826873
|
TATATA | T | 10 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(7): Show | 10 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+3433_12+3437del others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826873 | |||||
| chr6:157826878
|
A | AATATATA others(24): Show |
8 | a0001c0001t0001g0280a0001c0003t0003g0279a0001c0003t0003g0281others(5): Show | 8 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3461_12+3462ins others(31): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826878 | |||||
| chr6:157826878
|
A | AT | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3432_12+3433ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826878 | ||||||
| chr6:157826878
|
A | ATATATTA others(6): Show |
1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+3432_12+3433ins others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826878 | ||||||
| chr6:157826883
|
A | T | 17 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+3437A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826883 | ||||||
| chr6:157826884
|
T | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3438T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826884 | ||||||
| chr6:157826885
|
A | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3439A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826885 | ||||||
| chr6:157826886
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3440A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826886 | ||||||
| chr6:157826886
|
A | T | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12+3440A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826886 | ||||||
| chr6:157826888
|
T | TATATATT others(21): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03834.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.12+3497_12+3524dup others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826888 | |||||
| chr6:157826888
|
T | TATATATT others(50): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0157 | 2 | HG04115.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.12+3470_12+3471ins others(57): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826888 | |||||
| chr6:157826888
|
T | TATATATT others(743): Show |
1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.12+3470_12+3471ins others(750): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826888 | |||||
| chr6:157826892
|
T | C | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3446T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826892 | ||||||
| chr6:157826893
|
AT | A | 17 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+3449delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826893 | |||||
| chr6:157826895
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3449T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826895 | ||||||
| chr6:157826898
|
A | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3452A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826898 | ||||||
| chr6:157826899
|
G | T | 2 | a0001c0001t0011g0259a0001c0001t0018g0302 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+3453G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826899 | ||||||
| chr6:157826900
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3454T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826900 | ||||||
| chr6:157826901
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3455T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826901 | ||||||
| chr6:157826904
|
TATAATAT others(60): Show |
T | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+3462_12+3528del others(67): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826904 | |||||
| chr6:157826907
|
A | AT | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3461_12+3462ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826907 | ||||||
| chr6:157826907
|
A | ATATATTA others(6): Show |
1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+3461_12+3462ins others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826907 | ||||||
| chr6:157826907
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3461A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826907 | ||||||
| chr6:157826908
|
A | T | 17 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+3462A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826908 | ||||||
| chr6:157826910
|
A | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3464A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826910 | ||||||
| chr6:157826913
|
TA | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3471delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826913 | |||||
| chr6:157826915
|
AAATATAT others(49): Show |
A | 5 | a0001c0001t0005g0289a0001c0001t0005g0293a0001c0001t0021g0291others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+3471_12+3526del others(56): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826915 | |||||
| chr6:157826916
|
A | AT | 111 | a0001c0001t0001g0078a0001c0001t0001g0117a0001c0001t0001g0118others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.12+3470_12+3471ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826916 | ||||||
| chr6:157826916
|
A | ATATATAT others(23): Show |
7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01516.hp1 HG02602.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3470_12+3471ins others(30): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826916 | ||||||
| chr6:157826916
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3470A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826916 | ||||||
| chr6:157826917
|
A | C | 8 | a0001c0001t0001g0280a0001c0003t0003g0279a0001c0003t0003g0281others(5): Show | 8 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3471A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826917 | ||||||
| chr6:157826926
|
A | ATTT | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3480_12+3481ins others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826926 | ||||||
| chr6:157826929
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3483T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826929 | ||||||
| chr6:157826932
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3486T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826932 | ||||||
| chr6:157826935
|
A | T | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3489A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826935 | ||||||
| chr6:157826942
|
A | ACATATAT others(23): Show |
1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.12+3496_12+3497ins others(30): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826942 | ||||||
| chr6:157826943
|
A | C | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3497A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826943 | ||||||
| chr6:157826944
|
A | AATATATT others(78): Show |
2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.12+3524_12+3525ins others(85): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826944 | |||||
| chr6:157826944
|
A | AATATATT others(50): Show |
11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.12+3524_12+3525ins others(57): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826944 | |||||
| chr6:157826944
|
A | AATATATT others(22): Show |
1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.12+3583_12+3611dup others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826944 | |||||
| chr6:157826944
|
A | AC | 8 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0280others(5): Show | 8 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+3498_12+3499ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826944 | ||||||
| chr6:157826944
|
A | AT | 69 | a0001c0001t0001g0130a0001c0001t0001g0236a0001c0001t0003g0277others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.12+3498_12+3499ins others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826944 | ||||||
| chr6:157826944
|
A | ATATATAT others(482): Show |
1 | a0002c0002t0002g0044 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+3498_12+3499ins others(489): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826944 | ||||||
| chr6:157826944
|
A | ATATATAT others(453): Show |
1 | a0002c0002t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+3498_12+3499ins others(460): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826944 | ||||||
| chr6:157826944
|
A | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0151 | 2 | HG03540.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.12+3498A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826944 | ||||||
| chr6:157826945
|
A | C | 16 | a0001c0001t0001g0267a0001c0003t0003g0263a0001c0003t0003g0264others(13): Show | 16 | HG00099.hp2 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.12+3499A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826945 | ||||||
| chr6:157826954
|
AGTTTAT | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3509_12+3514del others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826954 | ||||||
| chr6:157826955
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3509G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826955 | ||||||
| chr6:157826965
|
T | A | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3519T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826965 | ||||||
| chr6:157826966
|
A | C | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3520A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826966 | ||||||
| chr6:157826966
|
A | G | 9 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270others(6): Show | 9 | HG02602.hp1 HG02735.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.12+3520A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826966 | ||||||
| chr6:157826970
|
AC | A | 19 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0001g0152others(16): Show | 19 | HG00280.hp2 HG00544.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.12+3525delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826970 | ||||||
| chr6:157826971
|
C | A | 108 | a0001c0001t0001g0130a0001c0001t0001g0234a0001c0001t0001g0235others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.12+3525C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826971 | ||||||
| chr6:157826971
|
C | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3525C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826971 | ||||||
| chr6:157826973
|
T | A | 19 | a0001c0001t0001g0061a0001c0001t0001g0078a0001c0001t0001g0152others(16): Show | 19 | HG00280.hp2 HG00544.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.12+3527T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826973 | ||||||
| chr6:157826973
|
T | C | 25 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3527T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826973 | ||||||
| chr6:157826973
|
T | TATATATT others(21): Show |
1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.12+3553_12+3554ins others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826973 | |||||
| chr6:157826974
|
A | C | 3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.12+3528A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826974 | ||||||
| chr6:157826976
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00408.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.12+3530A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826976 | ||||||
| chr6:157826983
|
A | G | 2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3537A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826983 | ||||||
| chr6:157826984
|
G | T | 2 | a0001c0001t0011g0259a0001c0001t0018g0302 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+3538G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826984 | ||||||
| chr6:157826986
|
T | TTA | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+3545_12+3546dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157826986 | |||||
| chr6:157826993
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12+3547A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826993 | ||||||
| chr6:157826997
|
A | G | 1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.12+3551A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826997 | ||||||
| chr6:157826997
|
A | T | 1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.12+3551A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826997 | ||||||
| chr6:157826999
|
AC | A | 3 | a0001c0001t0001g0152a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG00280.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3554delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157826999 | ||||||
| chr6:157827000
|
C | A | 136 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0119others(133): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.12+3554C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827000 | ||||||
| chr6:157827000
|
C | T | 2 | a0001c0001t0018g0302a0002c0007t0007g0054 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.12+3554C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827000 | ||||||
| chr6:157827001
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.12+3555A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827001 | ||||||
| chr6:157827002
|
T | A | 3 | a0001c0001t0001g0152a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG00280.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3556T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827002 | ||||||
| chr6:157827002
|
T | C | 54 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0119others(51): Show | 54 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.12+3556T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827002 | ||||||
| chr6:157827003
|
A | ATATAT | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3562_12+3566dup others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827003 | |||||
| chr6:157827005
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0233 | 2 | HG00408.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.12+3559A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827005 | ||||||
| chr6:157827008
|
TTATAGTT others(17): Show |
T | 3 | a0001c0003t0003g0255a0001c0003t0003g0256a0001c0003t0003g0299 | 3 | HG02145.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.12+3567_12+3590del others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827008 | |||||
| chr6:157827009
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3563T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827009 | ||||||
| chr6:157827012
|
A | G | 2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3566A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827012 | ||||||
| chr6:157827022
|
A | T | 10 | a0001c0001t0001g0157a0001c0001t0001g0206a0001c0001t0001g0207others(7): Show | 10 | HG00099.hp1 HG00323.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+3576A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827022 | ||||||
| chr6:157827023
|
T | TATATAAA others(20): Show |
5 | a0001c0003t0003g0266a0001c0003t0003g0272a0001c0003t0003g0284others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+3582_12+3583ins others(27): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827023 | |||||
| chr6:157827023
|
T | TATATAAA others(47): Show |
3 | a0001c0001t0001g0280a0001c0003t0003g0279a0001c0003t0003g0281 | 3 | HG01074.hp1 HG01106.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.12+3582_12+3583ins others(54): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827023 | |||||
| chr6:157827026
|
A | ATAAATAT others(22): Show |
1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.12+3582_12+3583ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827026 | |||||
| chr6:157827028
|
AC | A | 3 | a0001c0001t0005g0288a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG02572.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.12+3583delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827028 | ||||||
| chr6:157827029
|
C | A | 217 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.12+3583C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827029 | ||||||
| chr6:157827031
|
T | A | 3 | a0001c0001t0005g0288a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG02572.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.12+3585T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827031 | ||||||
| chr6:157827031
|
T | C | 136 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.12+3585T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827031 | ||||||
| chr6:157827031
|
T | TATATATT others(558): Show |
1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(565): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827031 | |||||
| chr6:157827031
|
T | TATATATT others(494): Show |
1 | a0001c0001t0001g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.12+3604_12+3605ins others(501): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827031 | |||||
| chr6:157827031
|
T | TATATTAT others(18): Show |
1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.12+3589_12+3590ins others(25): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827031 | |||||
| chr6:157827032
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3586A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827032 | ||||||
| chr6:157827033
|
T | TATATTAT others(47): Show |
1 | a0001c0003t0003g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+3609_12+3610ins others(54): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827033 | |||||
| chr6:157827038
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3592T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827038 | ||||||
| chr6:157827041
|
A | G | 3 | a0001c0001t0005g0288a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG02572.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.12+3595A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827041 | ||||||
| chr6:157827050
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3604A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827050 | ||||||
| chr6:157827050
|
AAT | A | 22 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(19): Show | 22 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.12+3610_12+3611del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827050 | |||||
| chr6:157827051
|
A | T | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0297others(1): Show | 4 | HG01123.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+3605A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827051 | ||||||
| chr6:157827052
|
T | TATATAAA others(20): Show |
6 | a0001c0001t0001g0267a0001c0001t0003g0277a0001c0001t0003g0278others(3): Show | 6 | HG00099.hp2 HG01175.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+3612_12+3638dup others(27): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827052 | |||||
| chr6:157827058
|
A | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0116 | 2 | HG01346.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.12+3612A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827058 | ||||||
| chr6:157827059
|
AC | A | 3 | a0001c0001t0005g0288a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG02572.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.12+3614delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827059 | ||||||
| chr6:157827060
|
C | T | 87 | a0001c0001t0001g0116a0001c0001t0003g0250a0001c0001t0003g0257others(84): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.12+3614C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827060 | ||||||
| chr6:157827070
|
A | G | 3 | a0001c0001t0005g0288a0001c0001t0005g0294a0001c0001t0005g0295 | 3 | HG02572.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.12+3624A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827070 | ||||||
| chr6:157827071
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3625G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827071 | ||||||
| chr6:157827079
|
AAT | A | 3 | a0001c0003t0003g0255a0001c0003t0003g0256a0001c0003t0003g0299 | 3 | HG02145.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.12+3639_12+3640del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827079 | |||||
| chr6:157827087
|
A | AACATATA others(355): Show |
1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.12+3648_12+3649ins others(362): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827087 | |||||
| chr6:157827087
|
A | AACATATA others(258): Show |
1 | a0001c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(265): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827087 | |||||
| chr6:157827087
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.12+3641A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827087 | ||||||
| chr6:157827087
|
AACAT | A | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3643_12+3646del others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827087 | |||||
| chr6:157827088
|
AC | A | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3643delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827088 | ||||||
| chr6:157827089
|
C | CATATATT others(475): Show |
1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(482): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(407): Show |
1 | a0005c0008t0006g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(414): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(440): Show |
1 | a0001c0001t0001g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(447): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(436): Show |
1 | a0005c0008t0006g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(443): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(484): Show |
1 | a0001c0001t0001g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(491): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(460): Show |
1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(467): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(645): Show |
1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(652): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(441): Show |
1 | a0001c0001t0001g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(448): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(465): Show |
1 | a0001c0001t0006g0097 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(472): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(489): Show |
1 | a0001c0001t0001g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(496): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(489): Show |
1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(496): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(470): Show |
1 | a0001c0001t0001g0087 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(477): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(412): Show |
1 | a0001c0001t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(419): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(527): Show |
1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(534): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(648): Show |
1 | a0001c0001t0001g0068 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(655): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(600): Show |
1 | a0001c0001t0001g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(607): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(499): Show |
1 | a0001c0001t0001g0125 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(506): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(528): Show |
1 | a0001c0001t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(535): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(470): Show |
1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(477): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(586): Show |
1 | a0001c0001t0010g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(593): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(499): Show |
1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(506): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(441): Show |
1 | a0001c0001t0001g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(448): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | CATATATT others(441): Show |
1 | a0001c0001t0001g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(448): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827089 | |||||
| chr6:157827089
|
C | T | 68 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.12+3643C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827089 | ||||||
| chr6:157827096
|
T | A | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+3650T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827096 | ||||||
| chr6:157827096
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3650T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827096 | ||||||
| chr6:157827099
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3653A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827099 | ||||||
| chr6:157827114
|
T | TAA | 9 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0081others(6): Show | 9 | HG01099.hp1 HG02451.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3669_12+3670ins others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827114 | |||||
| chr6:157827115
|
AC | A | 9 | a0001c0001t0001g0091a0001c0001t0005g0288a0001c0001t0005g0289others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3670delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827115 | ||||||
| chr6:157827116
|
C | A | 251 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.12+3670C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827116 | ||||||
| chr6:157827116
|
C | AACATATA others(494): Show |
1 | a0001c0001t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(501): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827116 | ||||||
| chr6:157827116
|
C | AACATATA others(541): Show |
1 | a0001c0001t0001g0232 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(548): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827116 | ||||||
| chr6:157827116
|
C | AACATATA others(581): Show |
1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(588): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827116 | ||||||
| chr6:157827116
|
C | AACATATA others(587): Show |
1 | a0001c0013t0001g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.12+3669_12+3670ins others(594): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827116 | ||||||
| chr6:157827118
|
T | A | 11 | a0001c0001t0001g0091a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01123.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.12+3672T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827118 | ||||||
| chr6:157827118
|
T | C | 176 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.12+3672T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827118 | ||||||
| chr6:157827118
|
T | CATATATT others(470): Show |
1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.12+3672delTinsCATA others(474): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827118 | ||||||
| chr6:157827118
|
T | CATATATT others(556): Show |
1 | a0001c0001t0001g0110 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.12+3672delTinsCATA others(560): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827118 | ||||||
| chr6:157827118
|
T | TATAGTTT others(15): Show |
1 | a0001c0001t0001g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.12+3675_12+3676ins others(22): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(613): Show |
1 | a0001c0001t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(620): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(461): Show |
1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(468): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(466): Show |
1 | a0001c0001t0001g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(473): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(468): Show |
1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(475): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(439): Show |
1 | a0001c0001t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(446): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(483): Show |
1 | a0001c0001t0010g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(490): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(434): Show |
1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(441): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827118
|
T | TATATTAT others(473): Show |
1 | a0001c0001t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.12+3676_12+3677ins others(480): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827118 | |||||
| chr6:157827120
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.12+3674T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827120 | ||||||
| chr6:157827121
|
ATATT | A | 3 | a0001c0003t0003g0255a0001c0003t0003g0256a0001c0003t0003g0299 | 3 | HG02145.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.12+3676_12+3679del others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827121 | ||||||
| chr6:157827123
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3677A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827123 | ||||||
| chr6:157827128
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3682A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827128 | ||||||
| chr6:157827129
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3683G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827129 | ||||||
| chr6:157827130
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3684T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827130 | ||||||
| chr6:157827131
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3685T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827131 | ||||||
| chr6:157827138
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3692A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827138 | ||||||
| chr6:157827139
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3693T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827139 | ||||||
| chr6:157827144
|
AC | A | 9 | a0001c0001t0001g0205a0001c0001t0005g0288a0001c0001t0005g0289others(6): Show | 9 | HG00544.hp2 HG01884.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.12+3699delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827144 | ||||||
| chr6:157827145
|
C | A | 270 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.12+3699C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827145 | ||||||
| chr6:157827145
|
C | AACATATA others(773): Show |
1 | a0001c0003t0003g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.12+3698_12+3699ins others(780): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827145 | ||||||
| chr6:157827145
|
C | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3699C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827145 | ||||||
| chr6:157827147
|
T | A | 8 | a0001c0001t0001g0205a0001c0001t0005g0288a0001c0001t0005g0289others(5): Show | 8 | HG00544.hp2 HG01884.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3701T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827147 | ||||||
| chr6:157827147
|
T | C | 192 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.12+3701T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827147 | ||||||
| chr6:157827147
|
T | CATATATT others(470): Show |
1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.12+3700_12+3701ins others(477): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827147 | ||||||
| chr6:157827147
|
T | TATAGTTT others(501): Show |
1 | a0001c0001t0001g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.12+3704_12+3705ins others(508): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827147 | |||||
| chr6:157827148
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.12+3702A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827148 | ||||||
| chr6:157827153
|
T | TTATAGTT others(17): Show |
1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+3712_12+3735dup others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827153 | |||||
| chr6:157827157
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3711A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827157 | ||||||
| chr6:157827158
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3712G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827158 | ||||||
| chr6:157827169
|
ATATAAAC others(13): Show |
A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3728_12+3747del others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827169 | |||||
| chr6:157827174
|
A | AACATATA others(440): Show |
1 | a0001c0001t0016g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.12+3822_12+3823ins others(447): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827174 | |||||
| chr6:157827174
|
A | AACATATA others(498): Show |
1 | a0001c0001t0001g0088 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(505): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827174 | |||||
| chr6:157827174
|
A | AACATATA others(394): Show |
1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.12+3932_12+3933ins others(401): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827174 | |||||
| chr6:157827174
|
A | AACATATA others(628): Show |
1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(635): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827174 | |||||
| chr6:157827174
|
A | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0010g0122 | 3 | HG01099.hp1 HG02129.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.12+3728A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827174 | ||||||
| chr6:157827175
|
AC | A | 4 | a0001c0001t0005g0289a0001c0001t0021g0291a0001c0003t0005g0290others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3730delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827175 | ||||||
| chr6:157827176
|
C | CATATATT others(441): Show |
1 | a0001c0001t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(448): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827176 | |||||
| chr6:157827176
|
C | CATATATT others(402): Show |
1 | a0001c0001t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(409): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827176 | |||||
| chr6:157827176
|
C | CATATATT others(436): Show |
1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.12+3880_12+3881ins others(443): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827176 | |||||
| chr6:157827176
|
C | CATATATT others(465): Show |
1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+3880_12+3881ins others(472): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827176 | |||||
| chr6:157827176
|
C | CATATATT others(441): Show |
1 | a0001c0001t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(448): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827176 | |||||
| chr6:157827176
|
C | T | 87 | a0001c0001t0001g0091a0001c0001t0003g0250a0001c0001t0003g0257others(84): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.12+3730C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827176 | ||||||
| chr6:157827182
|
T | TTATAGTT others(41): Show |
1 | a0001c0003t0003g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+3764_12+3765ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827182 | |||||
| chr6:157827182
|
T | TTATAGTT others(41): Show |
7 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3764_12+3765ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827182 | |||||
| chr6:157827182
|
T | TTATAGTT others(118): Show |
2 | a0001c0003t0003g0264a0001c0003t0003g0265 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.12+3793_12+3794ins others(125): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827182 | |||||
| chr6:157827182
|
T | TTATAGTT others(166): Show |
1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+3793_12+3794ins others(173): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827182 | |||||
| chr6:157827182
|
T | TTATAGTT others(99): Show |
1 | a0001c0003t0003g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.12+3822_12+3823ins others(106): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827182 | |||||
| chr6:157827184
|
A | ATAGTTTA others(457): Show |
1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+3758_12+3759ins others(464): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827184 | |||||
| chr6:157827185
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.12+3739T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827185 | ||||||
| chr6:157827186
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3740A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827186 | ||||||
| chr6:157827195
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3749A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827195 | ||||||
| chr6:157827203
|
A | AACATATA others(570): Show |
1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(577): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827203 | |||||
| chr6:157827203
|
A | AACATATA others(396): Show |
1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(403): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827203 | |||||
| chr6:157827203
|
A | AACATATA others(512): Show |
1 | a0001c0001t0001g0230 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(519): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827203 | |||||
| chr6:157827203
|
A | AATATATA others(296): Show |
1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+3758_12+3759ins others(303): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827203 | |||||
| chr6:157827203
|
A | AATATATA others(22): Show |
1 | a0002c0002t0002g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.12+3758_12+3759ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827203 | |||||
| chr6:157827203
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.12+3757A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827203 | ||||||
| chr6:157827204
|
AC | A | 4 | a0001c0001t0005g0289a0001c0001t0021g0291a0001c0003t0005g0290others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3759delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827204 | ||||||
| chr6:157827205
|
C | CATATATT others(411): Show |
1 | a0001c0001t0001g0100 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(418): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827205 | |||||
| chr6:157827205
|
C | CATATATT others(378): Show |
1 | a0001c0001t0001g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(385): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827205 | |||||
| chr6:157827205
|
C | T | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.12+3759C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827205 | ||||||
| chr6:157827211
|
T | TTATAGTT others(65): Show |
1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.12+3793_12+3794ins others(72): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827211 | |||||
| chr6:157827211
|
T | TTATAGTT others(41): Show |
4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01934.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+3793_12+3794ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827211 | |||||
| chr6:157827211
|
T | TTATAGTT others(46): Show |
1 | a0001c0003t0003g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.12+3770_12+3822dup others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827211 | |||||
| chr6:157827211
|
T | TTATAGTT others(70): Show |
3 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270 | 3 | HG04199.hp1 HG04204.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.12+3822_12+3823ins others(77): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827211 | |||||
| chr6:157827211
|
T | TTATAGTT others(70): Show |
1 | a0001c0003t0003g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.12+3809_12+3810ins others(77): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827211 | |||||
| chr6:157827215
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3769A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827215 | ||||||
| chr6:157827216
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3770G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827216 | ||||||
| chr6:157827227
|
ATATAAAC others(13): Show |
A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3786_12+3805del others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827227 | |||||
| chr6:157827230
|
TA | T | 4 | a0001c0001t0005g0289a0001c0001t0021g0291a0001c0003t0005g0290others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3787delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827230 | |||||
| chr6:157827232
|
A | AACATATA others(383): Show |
1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.12+3822_12+3823ins others(390): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827232 | |||||
| chr6:157827232
|
A | AACATATA others(599): Show |
1 | a0001c0001t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(606): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827232 | |||||
| chr6:157827234
|
C | CATATATT others(397): Show |
1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.12+3822_12+3823ins others(404): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827234 | |||||
| chr6:157827234
|
C | T | 89 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.12+3788C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827234 | ||||||
| chr6:157827236
|
T | TATATTAT others(49): Show |
1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.12+3795_12+3850dup others(56): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827236 | |||||
| chr6:157827236
|
T | TATATTAT others(590): Show |
1 | a0001c0001t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.12+3880_12+3881ins others(597): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827236 | |||||
| chr6:157827240
|
T | TTATAGTT others(17): Show |
3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.12+3799_12+3822dup others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827240 | |||||
| chr6:157827240
|
T | TTATAGTT others(41): Show |
1 | a0001c0003t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.12+3822_12+3823ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827240 | |||||
| chr6:157827244
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3798A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827244 | ||||||
| chr6:157827253
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3807A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827253 | ||||||
| chr6:157827261
|
A | AAATATAT others(367): Show |
1 | a0001c0001t0001g0236 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.12+3816_12+3817ins others(374): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827261
|
A | AAATATAT others(425): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18939.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.12+3816_12+3817ins others(432): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827261
|
A | AACATATA others(425): Show |
1 | a0001c0001t0001g0166 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.12+3903_12+3904ins others(432): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827261
|
A | AACATATA others(599): Show |
1 | a0001c0001t0001g0229 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(606): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827261
|
A | AACATATA others(482): Show |
1 | a0001c0001t0001g0171 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(489): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827261
|
A | AACATATA others(627): Show |
1 | a0001c0001t0001g0217 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.12+3959_12+3960ins others(634): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827261 | |||||
| chr6:157827263
|
C | T | 89 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.12+3817C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827263 | ||||||
| chr6:157827273
|
A | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+3827A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827273 | ||||||
| chr6:157827274
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3828G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827274 | ||||||
| chr6:157827277
|
T | TATATAAT others(494): Show |
1 | a0001c0001t0001g0083 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(501): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827277 | |||||
| chr6:157827283
|
A | ATATATAA others(22): Show |
1 | a0001c0001t0001g0280 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.12+3865_12+3866ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827283 | |||||
| chr6:157827283
|
A | ATATATAA others(51): Show |
1 | a0001c0003t0003g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.12+3865_12+3866ins others(58): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827283 | |||||
| chr6:157827285
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3839A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827285 | ||||||
| chr6:157827290
|
A | AACATATA others(483): Show |
1 | a0001c0001t0001g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.12+3906_12+3907ins others(490): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827290 | |||||
| chr6:157827290
|
A | C | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | NA18939.hp2 NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.12+3844A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827290 | ||||||
| chr6:157827292
|
C | CATATAGT others(296): Show |
1 | a0001c0001t0001g0102 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.12+3851_12+3852ins others(303): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827292 | |||||
| chr6:157827292
|
C | CATATATT others(437): Show |
1 | a0001c0001t0001g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.12+3938_12+3939ins others(444): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827292 | |||||
| chr6:157827292
|
C | T | 89 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.12+3846C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827292 | ||||||
| chr6:157827302
|
A | G | 5 | a0001c0001t0005g0289a0001c0001t0005g0293a0001c0001t0021g0291others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+3856A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827302 | ||||||
| chr6:157827303
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3857G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827303 | ||||||
| chr6:157827306
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.12+3860T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827306 | ||||||
| chr6:157827306
|
T | TATATAAT others(513): Show |
1 | a0001c0001t0001g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.12+3880_12+3881ins others(520): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827306 | |||||
| chr6:157827306
|
T | TATATAAT others(557): Show |
1 | a0001c0001t0001g0117 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.12+3880_12+3881ins others(564): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827306 | |||||
| chr6:157827312
|
A | ATATATAA others(22): Show |
1 | a0001c0003t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+3894_12+3895ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827312 | |||||
| chr6:157827314
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3868A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827314 | ||||||
| chr6:157827318
|
A | AAACATAT others(21): Show |
1 | a0003c0006t0001g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+3875_12+3902dup others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827318 | |||||
| chr6:157827319
|
A | AACATATA others(425): Show |
1 | a0001c0001t0001g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(432): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATATA others(454): Show |
1 | a0001c0001t0001g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(461): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATATA others(570): Show |
1 | a0001c0001t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(577): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATATA others(481): Show |
1 | a0001c0001t0001g0220 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(488): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATATA others(510): Show |
1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(517): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATATA others(453): Show |
1 | a0001c0001t0001g0172 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(460): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | AACATGTA others(513): Show |
1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12+3877_12+3878ins others(520): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827319 | |||||
| chr6:157827319
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18939.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.12+3873A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827319 | ||||||
| chr6:157827321
|
C | T | 89 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.12+3875C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827321 | ||||||
| chr6:157827331
|
A | G | 5 | a0001c0001t0005g0289a0001c0001t0005g0293a0001c0001t0021g0291others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+3885A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827331 | ||||||
| chr6:157827332
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3886G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827332 | ||||||
| chr6:157827333
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.12+3887T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827333 | ||||||
| chr6:157827335
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0083a0001c0001t0001g0117 | 3 | NA18942.hp1 NA18983.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.12+3889T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827335 | ||||||
| chr6:157827335
|
T | TATATAAT others(557): Show |
1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(564): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827335 | |||||
| chr6:157827335
|
T | TATATAAT others(533): Show |
1 | a0001c0001t0001g0118 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(540): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827335 | |||||
| chr6:157827335
|
T | TATATAAT others(475): Show |
1 | a0001c0001t0001g0107 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(482): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827335 | |||||
| chr6:157827335
|
T | TATATAAT others(447): Show |
1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(454): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827335 | |||||
| chr6:157827341
|
A | ATATATAA others(51): Show |
2 | a0001c0003t0003g0286a0004c0005t0003g0282 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.12+3952_12+3953ins others(58): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827341 | |||||
| chr6:157827341
|
A | ATATATAA others(22): Show |
2 | a0001c0001t0001g0267a0001c0003t0003g0279 | 2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.12+3923_12+3924ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827341 | |||||
| chr6:157827341
|
A | ATATATAA others(80): Show |
1 | a0004c0005t0003g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.12+3923_12+3924ins others(87): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827341 | |||||
| chr6:157827341
|
A | T | 1 | a0001c0003t0003g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.12+3895A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827341 | ||||||
| chr6:157827343
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3897A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827343 | ||||||
| chr6:157827347
|
A | AAACATAT others(21): Show |
7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3904_12+3931dup others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827347 | |||||
| chr6:157827348
|
A | AACATATA others(425): Show |
1 | a0001c0001t0014g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.12+3961_12+3962ins others(432): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827348 | |||||
| chr6:157827348
|
A | AACATATA others(452): Show |
1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.12+3990_12+3991ins others(459): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827348 | |||||
| chr6:157827348
|
A | AACATATA others(481): Show |
2 | a0001c0001t0001g0221a0001c0004t0001g0170 | 2 | NA19063.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.12+3990_12+3991ins others(488): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827348 | |||||
| chr6:157827348
|
A | AACATATA others(570): Show |
1 | a0001c0001t0001g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.12+3935_12+3936ins others(577): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827348 | |||||
| chr6:157827348
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12+3902A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827348 | ||||||
| chr6:157827350
|
C | CATATAGT others(378): Show |
1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.12+3909_12+3910ins others(385): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827350 | |||||
| chr6:157827350
|
C | T | 89 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(86): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.12+3904C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827350 | ||||||
| chr6:157827356
|
TTATAGTT others(152): Show |
T | 2 | a0001c0001t0005g0294a0001c0001t0005g0295 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.12+3944_12+4102del | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827356 | |||||
| chr6:157827360
|
A | G | 3 | a0001c0001t0005g0293a0001c0001t0021g0291a0001c0003t0022g0292 | 3 | HG01884.hp1 HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.12+3914A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827360 | ||||||
| chr6:157827361
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3915G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827361 | ||||||
| chr6:157827362
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.12+3916T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827362 | ||||||
| chr6:157827364
|
T | C | 9 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(6): Show | 9 | NA18942.hp1 NA18947.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3918T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827364 | ||||||
| chr6:157827370
|
A | ATATATAA others(51): Show |
1 | a0001c0003t0003g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.12+3952_12+3953ins others(58): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827370 | |||||
| chr6:157827370
|
A | T | 1 | a0001c0003t0003g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.12+3924A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827370 | ||||||
| chr6:157827372
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3926A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827372 | ||||||
| chr6:157827376
|
A | AAACATAT others(21): Show |
3 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG01934.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.12+3933_12+3960dup others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827376 | |||||
| chr6:157827377
|
A | AACATGTA others(513): Show |
1 | a0001c0001t0004g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12+3935_12+3936ins others(520): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827377 | |||||
| chr6:157827377
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12+3931A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827377 | ||||||
| chr6:157827379
|
C | T | 87 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(84): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.12+3933C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827379 | ||||||
| chr6:157827382
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.12+3936A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827382 | ||||||
| chr6:157827385
|
T | TTATAGTT others(17): Show |
2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+3944_12+3967dup others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827385 | |||||
| chr6:157827385
|
TTATAGTT others(123): Show |
T | 1 | a0001c0001t0005g0288 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+3973_12+4102del | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827385 | |||||
| chr6:157827389
|
A | G | 2 | a0001c0001t0005g0293a0001c0003t0022g0292 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.12+3943A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827389 | ||||||
| chr6:157827390
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3944G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827390 | ||||||
| chr6:157827393
|
T | C | 9 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(6): Show | 9 | NA18942.hp1 NA18947.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3947T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827393 | ||||||
| chr6:157827399
|
A | T | 3 | a0001c0003t0003g0286a0004c0005t0003g0282a0004c0005t0003g0283 | 3 | HG00099.hp2 HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.12+3953A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827399 | ||||||
| chr6:157827401
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3955A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827401 | ||||||
| chr6:157827406
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0004g0211 | 2 | HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.12+3960A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827406 | ||||||
| chr6:157827408
|
C | T | 86 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.12+3962C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827408 | ||||||
| chr6:157827411
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.12+3965A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827411 | ||||||
| chr6:157827413
|
A | ATTATAGT others(41): Show |
1 | a0001c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.12+3981_12+3982ins others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827413 | |||||
| chr6:157827419
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3973G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827419 | ||||||
| chr6:157827421
|
T | TTA | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3980_12+3981dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827421 | |||||
| chr6:157827422
|
T | C | 5 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(2): Show | 5 | NA18948.hp1 NA18983.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+3976T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827422 | ||||||
| chr6:157827428
|
A | T | 2 | a0001c0003t0003g0275a0001c0003t0003g0285 | 2 | HG01175.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.12+3982A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827428 | ||||||
| chr6:157827430
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+3984A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827430 | ||||||
| chr6:157827435
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12+3989A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827435 | ||||||
| chr6:157827437
|
C | T | 86 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.12+3991C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827437 | ||||||
| chr6:157827438
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.12+3992A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827438 | ||||||
| chr6:157827438
|
ATATATTA others(99): Show |
A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+4020_12+4125del | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827438 | |||||
| chr6:157827440
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.12+3994A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827440 | ||||||
| chr6:157827442
|
A | AGTTTATA others(12): Show |
1 | a0001c0001t0001g0121 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.12+3996_12+3997ins others(19): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827442 | ||||||
| chr6:157827442
|
A | ATTATAGT others(128): Show |
1 | a0001c0001t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(135): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(142): Show |
1 | a0001c0001t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(149): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(41): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG00544.hp1 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+4021_12+4068dup others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(65): Show |
1 | a0001c0001t0001g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.12+3997_12+4068dup others(72): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(113): Show |
1 | a0001c0001t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(120): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(137): Show |
1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(144): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827442
|
A | ATTATAGT others(423): Show |
1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12+4017_12+4018ins others(430): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827442 | |||||
| chr6:157827443
|
TTATAGTT others(65): Show |
T | 5 | a0001c0001t0005g0289a0001c0001t0005g0293a0001c0001t0021g0291others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+4021_12+4092del others(72): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827443 | |||||
| chr6:157827447
|
AGTTTATA others(60): Show |
A | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+4002_12+4068del others(67): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827447 | ||||||
| chr6:157827448
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4002G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827448 | ||||||
| chr6:157827451
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0107 | 2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.12+4005T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827451 | ||||||
| chr6:157827457
|
A | ATATATAA others(46): Show |
1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827457 | |||||
| chr6:157827457
|
A | T | 3 | a0001c0003t0003g0274a0001c0003t0003g0275a0001c0003t0003g0286 | 3 | HG00099.hp2 HG02735.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.12+4011A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827457 | ||||||
| chr6:157827459
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4013A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827459 | ||||||
| chr6:157827463
|
AAACTTAT others(33): Show |
A | 1 | a0001c0001t0019g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+4020_12+4059del others(40): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827463 | |||||
| chr6:157827465
|
A | AATATATT others(458): Show |
1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(465): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(516): Show |
2 | a0001c0001t0001g0174a0001c0004t0001g0173 | 2 | NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.12+4019_12+4020ins others(523): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(487): Show |
3 | a0001c0001t0001g0205a0001c0004t0001g0176a0001c0004t0001g0177 | 3 | HG00544.hp2 NA18947.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.12+4019_12+4020ins others(494): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(632): Show |
1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(639): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(574): Show |
1 | a0001c0001t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(581): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(488): Show |
1 | a0001c0001t0001g0238 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(495): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(488): Show |
1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(495): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(604): Show |
1 | a0001c0001t0001g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(611): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(430): Show |
1 | a0001c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(437): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(547): Show |
1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(554): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(543): Show |
1 | a0001c0001t0001g0240 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(550): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | AATATATT others(574): Show |
1 | a0001c0001t0001g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(581): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATAT | 64 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.12+4019_12+4020ins others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(460): Show |
1 | a0001c0012t0001g0202 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(467): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(27): Show |
1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(114): Show |
1 | a0001c0001t0004g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(121): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(172): Show |
1 | a0001c0001t0004g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(179): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(201): Show |
2 | a0001c0001t0004g0262a0001c0009t0006g0058 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.12+4019_12+4020ins others(208): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
A | ATATATAT others(375): Show |
1 | a0002c0002t0002g0030 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.12+4019_12+4020ins others(382): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827465
|
ACTTATAG others(26): Show |
A | 2 | a0001c0001t0004g0065a0001c0001t0004g0066 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+4020_12+4052del others(33): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827465 | ||||||
| chr6:157827466
|
C | A | 86 | a0001c0001t0001g0153a0001c0001t0001g0164a0001c0001t0001g0174others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.12+4020C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATA | 47 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0102others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(659): Show |
1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(666): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(517): Show |
1 | a0001c0001t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(524): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(488): Show |
1 | a0001c0001t0001g0222 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(495): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(546): Show |
1 | a0001c0001t0001g0231 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(553): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(575): Show |
1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(582): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(576): Show |
1 | a0001c0001t0001g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(583): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(692): Show |
1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(699): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(574): Show |
1 | a0001c0001t0001g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(581): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(27): Show |
1 | a0003c0006t0001g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(690): Show |
1 | a0001c0001t0001g0223 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(697): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(545): Show |
1 | a0001c0001t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(552): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(572): Show |
1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(579): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(661): Show |
1 | a0001c0001t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(668): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(604): Show |
1 | a0001c0001t0001g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(611): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(662): Show |
1 | a0001c0001t0001g0206 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(669): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(575): Show |
1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(582): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(517): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(524): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(749): Show |
1 | a0001c0001t0015g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(756): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(547): Show |
1 | a0001c0001t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(554): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(56): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(63): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(776): Show |
1 | a0001c0001t0001g0161 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(783): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(603): Show |
1 | a0001c0001t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(610): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(604): Show |
1 | a0001c0001t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(611): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(716): Show |
1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(723): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(648): Show |
1 | a0001c0001t0009g0132 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(655): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(1066): Show |
1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(1073): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(648): Show |
1 | a0001c0001t0009g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(655): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(692): Show |
1 | a0001c0001t0001g0218 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(699): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(575): Show |
1 | a0001c0001t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(582): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(807): Show |
1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(814): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(1095): Show |
1 | a0001c0001t0001g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(1102): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(114): Show |
6 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01934.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(121): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(743): Show |
1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(750): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(719): Show |
1 | a0001c0001t0001g0246 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(726): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(662): Show |
1 | a0001c0001t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(669): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(691): Show |
1 | a0001c0001t0001g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(698): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(664): Show |
1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(671): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(143): Show |
8 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG02451.hp2 HG02602.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(150): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(691): Show |
1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(698): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(172): Show |
3 | a0001c0001t0001g0136a0001c0003t0003g0264a0001c0003t0003g0268 | 3 | HG02572.hp1 HG02965.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(179): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(201): Show |
1 | a0001c0003t0003g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(208): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(633): Show |
1 | a0001c0001t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(640): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(230): Show |
2 | a0001c0001t0003g0278a0001c0001t0003g0296 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(237): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(288): Show |
1 | a0001c0001t0003g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(295): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(578): Show |
1 | a0001c0001t0001g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(585): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(201): Show |
1 | a0004c0005t0003g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(208): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(172): Show |
1 | a0001c0003t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(179): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(720): Show |
1 | a0001c0001t0001g0249 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(727): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(749): Show |
1 | a0001c0001t0001g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(756): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(721): Show |
1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(728): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(143): Show |
1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(150): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(517): Show |
1 | a0001c0001t0001g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(524): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(720): Show |
1 | a0001c0001t0001g0216 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(727): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(114): Show |
3 | a0001c0001t0001g0267a0001c0003t0003g0284a0004c0005t0003g0283 | 3 | HG00642.hp2 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(121): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(633): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.12+4020_12+4021ins others(640): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(691): Show |
1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(698): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(692): Show |
1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(699): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(720): Show |
1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(727): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(662): Show |
1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(669): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(56): Show |
1 | a0001c0001t0001g0280 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(63): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(604): Show |
1 | a0001c0001t0001g0199 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(611): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(633): Show |
1 | a0001c0001t0001g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(640): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(27): Show |
1 | a0001c0003t0003g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(259): Show |
1 | a0001c0003t0003g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(266): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827466
|
C | CATATATT others(317): Show |
1 | a0001c0003t0003g0285 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.12+4020_12+4021ins others(324): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827466 | ||||||
| chr6:157827467
|
T | A | 2 | a0001c0001t0001g0167a0001c0003t0003g0273 | 2 | HG02615.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.12+4021T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827467 | ||||||
| chr6:157827471
|
AGTTTATA others(36): Show |
A | 1 | a0001c0003t0003g0273 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.12+4026_12+4068del others(43): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827471 | ||||||
| chr6:157827472
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4026G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827472 | ||||||
| chr6:157827474
|
T | TTA | 3 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0013g0298 | 3 | HG02280.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.12+4033_12+4034dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827474 | |||||
| chr6:157827483
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4037A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827483 | ||||||
| chr6:157827489
|
A | ATATAT | 64 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.12+4043_12+4044ins others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827489 | ||||||
| chr6:157827489
|
ACTTATAG others(2): Show |
A | 6 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(3): Show | 6 | HG02280.hp2 HG02559.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+4044_12+4052del others(9): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827489 | ||||||
| chr6:157827490
|
C | A | 64 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.12+4044C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827490 | ||||||
| chr6:157827490
|
C | CATATA | 149 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0092others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.12+4044_12+4045ins others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827490 | ||||||
| chr6:157827490
|
C | CATATATT others(3): Show |
1 | a0001c0001t0001g0236 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.12+4044_12+4045ins others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827490 | ||||||
| chr6:157827490
|
C | CATATATT others(691): Show |
1 | a0001c0001t0001g0150 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.12+4044_12+4045ins others(698): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827490 | ||||||
| chr6:157827490
|
C | CTATATTA others(518): Show |
1 | a0001c0001t0001g0201 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.12+4045_12+4046ins others(525): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(46): Show |
6 | a0001c0001t0001g0089a0001c0001t0001g0098a0001c0001t0001g0101others(3): Show | 6 | HG01081.hp1 NA18983.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+4068_12+4069ins others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(75): Show |
1 | a0001c0001t0001g0100 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(82): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(70): Show |
1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(77): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(94): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0116 | 2 | HG01346.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.12+4068_12+4069ins others(101): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(128): Show |
1 | a0001c0001t0001g0094 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(135): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(157): Show |
1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(164): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827490
|
C | CTTATAGT others(142): Show |
1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(149): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827490 | |||||
| chr6:157827496
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4050G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827496 | ||||||
| chr6:157827505
|
A | T | 8 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+4059A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827505 | ||||||
| chr6:157827507
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4061A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827507 | ||||||
| chr6:157827510
|
TAAACA | T | 8 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+4065_12+4069del others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827510 | ||||||
| chr6:157827514
|
C | CTTATAGT others(22): Show |
1 | a0001c0001t0001g0125 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(29): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | CTTATAGT others(85): Show |
1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(92): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | CTTATAGT others(75): Show |
1 | a0001c0001t0001g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(82): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | CTTATAGT others(80): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0124 | 2 | NA19010.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.12+4068_12+4069ins others(87): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | CTTATAGT others(104): Show |
1 | a0001c0001t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(111): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | CTTATAGT others(128): Show |
1 | a0001c0001t0001g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.12+4068_12+4069ins others(135): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827514
|
C | T | 64 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.12+4068C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827514 | ||||||
| chr6:157827515
|
A | ATATAT | 202 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0100others(199): Show | 202 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(230): Show |
1 | a0001c0001t0001g0102 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(237): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(27): Show |
1 | a0001c0001t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(783): Show |
1 | a0001c0001t0001g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(790): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(61): Show |
1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(68): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(56): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0115 | 2 | HG01106.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(63): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(899): Show |
1 | a0001c0001t0001g0152 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(906): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(85): Show |
1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(92): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(90): Show |
4 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG01257.hp2 HG04204.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(97): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(61): Show |
12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0072others(9): Show | 12 | HG02080.hp1 HG03834.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(68): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(32): Show |
8 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(5): Show | 8 | HG00438.hp1 HG01496.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(39): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(666): Show |
1 | a0001c0001t0001g0228 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(673): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(423): Show |
1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.12+4073_12+4074ins others(430): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATATATTA others(3): Show |
26 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0084others(23): Show | 26 | HG00544.hp1 HG00558.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.12+4073_12+4074ins others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | ATGTATTA others(523): Show |
1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.12+4070_12+4071ins others(530): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827515 | |||||
| chr6:157827515
|
A | T | 18 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0081others(15): Show | 18 | HG02055.hp2 HG02080.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+4069A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827515 | ||||||
| chr6:157827520
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4074G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827520 | ||||||
| chr6:157827522
|
T | TTA | 6 | a0001c0001t0001g0168a0001c0001t0001g0222a0001c0001t0003g0250others(3): Show | 6 | HG02280.hp2 HG02970.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+4081_12+4082dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827522 | |||||
| chr6:157827529
|
A | T | 6 | a0001c0001t0001g0073a0001c0001t0001g0147a0001c0001t0001g0239others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+4083A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827529 | ||||||
| chr6:157827531
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4085A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827531 | ||||||
| chr6:157827537
|
ACATATAT others(5): Show |
A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4092_12+4103del others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827537 | ||||||
| chr6:157827538
|
C | T | 99 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(96): Show | 99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.12+4092C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827538 | ||||||
| chr6:157827539
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.12+4093A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827539 | ||||||
| chr6:157827539
|
ATATAT | A | 7 | a0001c0004t0001g0170a0001c0004t0001g0173a0001c0004t0001g0176others(4): Show | 7 | HG00280.hp1 HG01123.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+4103_12+4107del others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827539 | |||||
| chr6:157827543
|
A | AGTTTATA others(147): Show |
1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.12+4097_12+4098ins others(154): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827543 | ||||||
| chr6:157827544
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0248 | 2 | HG02735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.12+4098T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827544 | ||||||
| chr6:157827544
|
T | TTATAGTT others(536): Show |
1 | a0006c0014t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(543): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(681): Show |
1 | a0001c0011t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(688): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(768): Show |
1 | a0001c0001t0001g0213 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(775): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(826): Show |
1 | a0001c0001t0001g0212 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(833): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(477): Show |
1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(484): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(506): Show |
1 | a0003c0006t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(513): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(191): Show |
1 | a0001c0003t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(198): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(17): Show |
1 | a0002c0002t0002g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(46): Show |
3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(104): Show |
1 | a0002c0002t0002g0042 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(111): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(162): Show |
1 | a0002c0002t0002g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(169): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(191): Show |
2 | a0002c0002t0002g0041a0002c0002t0002g0051 | 2 | NA18987.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(198): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(220): Show |
2 | a0002c0002t0002g0039a0002c0002t0002g0040 | 2 | NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(227): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(249): Show |
2 | a0002c0002t0002g0037a0002c0002t0002g0038 | 2 | HG02015.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(256): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(278): Show |
3 | a0002c0002t0002g0035a0002c0002t0002g0036a0002c0002t0002g0055 | 3 | HG02083.hp2 HG02132.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(285): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(307): Show |
4 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0034others(1): Show | 4 | HG00423.hp1 HG03654.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(314): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(336): Show |
1 | a0002c0002t0002g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(343): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(365): Show |
2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG01358.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(372): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(394): Show |
2 | a0002c0002t0002g0027a0002c0002t0002g0056 | 2 | HG00642.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(401): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(423): Show |
4 | a0002c0002t0002g0023a0002c0002t0002g0025a0002c0002t0002g0026others(1): Show | 4 | HG00733.hp2 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(430): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(452): Show |
2 | a0002c0002t0002g0021a0002c0002t0008g0022 | 2 | HG00735.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(459): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(481): Show |
2 | a0002c0002t0002g0018a0002c0002t0012g0050 | 2 | HG03834.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(488): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(510): Show |
3 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017 | 3 | HG00621.hp1 HG02129.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(517): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(539): Show |
3 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014 | 3 | HG00438.hp2 HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(546): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(568): Show |
2 | a0002c0002t0002g0010a0002c0002t0002g0011 | 2 | HG00408.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(575): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(597): Show |
6 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0006others(3): Show | 6 | HG00673.hp1 NA18939.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(604): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(626): Show |
1 | a0002c0002t0002g0003 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(633): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(655): Show |
1 | a0002c0002t0002g0002 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(662): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(713): Show |
1 | a0002c0002t0002g0001 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.12+4102_12+4103ins others(720): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827544
|
T | TTATAGTT others(509): Show |
2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.12+4102_12+4103ins others(516): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827544 | |||||
| chr6:157827549
|
T | G | 8 | a0001c0001t0001g0167a0001c0001t0001g0200a0001c0001t0001g0223others(5): Show | 8 | HG00423.hp2 HG01243.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+4103T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827549 | ||||||
| chr6:157827551
|
A | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0200a0001c0001t0001g0223others(1): Show | 4 | HG00423.hp2 HG02523.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4105A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827551 | ||||||
| chr6:157827553
|
AGTT | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0200a0001c0001t0001g0223others(1): Show | 4 | HG00423.hp2 HG02523.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4108_12+4110del others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827553 | ||||||
| chr6:157827554
|
G | GTT | 4 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0057others(1): Show | 4 | HG02280.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+4110_12+4111dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827554 | |||||
| chr6:157827554
|
G | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4108G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827554 | ||||||
| chr6:157827556
|
T | TTA | 165 | a0001c0001t0001g0061a0001c0001t0001g0134a0001c0001t0001g0135others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.12+4115_12+4116dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827556 | |||||
| chr6:157827565
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4119A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827565 | ||||||
| chr6:157827572
|
T | C | 50 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099others(47): Show | 50 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.12+4126T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827572 | ||||||
| chr6:157827578
|
T | TTATATTA others(24): Show |
1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.12+4152_12+4153ins others(31): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827578 | |||||
| chr6:157827582
|
A | AGT | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4136_12+4137ins others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827582 | ||||||
| chr6:157827583
|
T | G | 4 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4137T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827583 | ||||||
| chr6:157827587
|
A | ATAAT | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4141_12+4142ins others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827587 | ||||||
| chr6:157827588
|
G | A | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4142G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827588 | ||||||
| chr6:157827590
|
T | A | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4144T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827590 | ||||||
| chr6:157827592
|
A | T | 56 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.12+4146A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827592 | ||||||
| chr6:157827593
|
T | A | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4147T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827593 | ||||||
| chr6:157827602
|
G | T | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4156G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827602 | ||||||
| chr6:157827603
|
A | ATAGTTTA others(3): Show |
3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4157_12+4158ins others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827603 | ||||||
| chr6:157827604
|
G | A | 3 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0002t0002g0047 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.12+4158G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827604 | ||||||
| chr6:157827660
|
T | C | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4214T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827660 | ||||||
| chr6:157827730
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4284G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827730 | ||||||
| chr6:157827744
|
A | G | 116 | a0001c0001t0001g0087a0001c0001t0001g0267a0001c0001t0001g0280others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.12+4298A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827744 | ||||||
| chr6:157827856
|
C | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+4410C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157827856 | ||||||
| chr6:157827862
|
CT | C | 88 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(85): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.12+4431delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157827862 | |||||
| chr6:157828079
|
C | A | 114 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0250others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.12+4633C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828079 | ||||||
| chr6:157828079
|
C | G | 1 | a0002c0002t0002g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.12+4633C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828079 | ||||||
| chr6:157828148
|
T | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4702T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828148 | ||||||
| chr6:157828211
|
G | GTGTT | 116 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0267others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.12+4768_12+4769ins others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157828211 | |||||
| chr6:157828216
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+4770C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828216 | ||||||
| chr6:157828305
|
T | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4859T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828305 | ||||||
| chr6:157828306
|
G | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4860G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828306 | ||||||
| chr6:157828307
|
T | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4861T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828307 | ||||||
| chr6:157828308
|
T | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4862T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828308 | ||||||
| chr6:157828309
|
G | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4863G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828309 | ||||||
| chr6:157828310
|
C | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+4864C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828310 | ||||||
| chr6:157828375
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.12+4929A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828375 | ||||||
| chr6:157828504
|
T | A | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+5058T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828504 | ||||||
| chr6:157828556
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.12+5110C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828556 | ||||||
| chr6:157828586
|
C | G | 1 | a0001c0001t0010g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.12+5140C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828586 | ||||||
| chr6:157828654
|
C | T | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+5208C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828654 | ||||||
| chr6:157828720
|
C | T | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.12+5274C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828720 | ||||||
| chr6:157828794
|
G | A | 1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+5348G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828794 | ||||||
| chr6:157828798
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0100 | 2 | HG02273.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.12+5352A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828798 | ||||||
| chr6:157828801
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.12+5355C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828801 | ||||||
| chr6:157828809
|
C | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+5363C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828809 | ||||||
| chr6:157828814
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.12+5368G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828814 | ||||||
| chr6:157828917
|
T | A | 2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+5471T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828917 | ||||||
| chr6:157828955
|
C | T | 1 | a0001c0001t0010g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.12+5509C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828955 | ||||||
| chr6:157828969
|
A | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+5523A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828969 | ||||||
| chr6:157828983
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+5537A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157828983 | ||||||
| chr6:157829108
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.12+5662G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829108 | ||||||
| chr6:157829144
|
T | TGGCAATT others(305): Show |
1 | a0001c0001t0004g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.12+5714_12+5715ins others(312): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157829144 | |||||
| chr6:157829144
|
T | TGGCAATT others(306): Show |
12 | a0001c0001t0003g0257a0001c0001t0004g0063a0001c0001t0004g0066others(9): Show | 12 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.12+5714_12+5715ins others(313): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157829144 | |||||
| chr6:157829144
|
T | TGGCAATT others(307): Show |
3 | a0001c0001t0003g0250a0001c0003t0003g0254a0001c0003t0003g0256 | 3 | HG02055.hp2 HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.12+5714_12+5715ins others(314): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157829144 | |||||
| chr6:157829145
|
G | A | 25 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0277others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+5699G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829145 | ||||||
| chr6:157829206
|
T | C | 8 | a0002c0002t0002g0032a0002c0002t0002g0035a0002c0002t0002g0037others(5): Show | 8 | HG00423.hp1 HG02083.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+5760T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829206 | ||||||
| chr6:157829251
|
A | G | 58 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.12+5805A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829251 | ||||||
| chr6:157829270
|
A | G | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+5824A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829270 | ||||||
| chr6:157829276
|
T | C | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+5830T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829276 | ||||||
| chr6:157829280
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.12+5834A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829280 | ||||||
| chr6:157829406
|
C | A | 4 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+5960C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829406 | ||||||
| chr6:157829452
|
A | G | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+6006A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829452 | ||||||
| chr6:157829506
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.12+6060C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829506 | ||||||
| chr6:157829643
|
A | G | 7 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0294others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+6197A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829643 | ||||||
| chr6:157829647
|
G | A | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12+6201G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829647 | ||||||
| chr6:157829942
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.12+6496C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157829942 | ||||||
| chr6:157830109
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.12+6663A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830109 | ||||||
| chr6:157830181
|
G | A | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+6735G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830181 | ||||||
| chr6:157830204
|
T | G | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+6758T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830204 | ||||||
| chr6:157830288
|
C | T | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+6842C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830288 | ||||||
| chr6:157830442
|
T | C | 38 | a0001c0001t0001g0153a0001c0001t0001g0162a0001c0001t0001g0164others(35): Show | 38 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.12+6996T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830442 | ||||||
| chr6:157830526
|
G | A | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+7080G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830526 | ||||||
| chr6:157830604
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG01934.hp1 HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.12+7158C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830604 | ||||||
| chr6:157830840
|
A | G | 3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.12+7394A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830840 | ||||||
| chr6:157830919
|
A | G | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+7473A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157830919 | ||||||
| chr6:157831035
|
T | G | 15 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.12+7589T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831035 | ||||||
| chr6:157831228
|
TC | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(7): Show | 10 | NA18942.hp1 NA18947.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+7784delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157831228 | |||||
| chr6:157831231
|
T | C | 2 | a0001c0001t0018g0302a0001c0010t0001g0059 | 2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+7785T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831231 | ||||||
| chr6:157831324
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA19060.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.12+7878T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831324 | ||||||
| chr6:157831446
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.12+8000C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831446 | ||||||
| chr6:157831566
|
G | A | 1 | a0001c0003t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+8120G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831566 | ||||||
| chr6:157831637
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0018g0302a0001c0010t0001g0059 | 3 | HG03041.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.12+8191G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831637 | ||||||
| chr6:157831703
|
C | T | 1 | a0001c0003t0003g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.12+8257C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157831703 | ||||||
| chr6:157832271
|
G | A | 2 | a0002c0002t0002g0010a0002c0002t0002g0023 | 2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.12+8825G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157832271 | ||||||
| chr6:157832299
|
C | T | 61 | a0001c0001t0011g0259a0001c0001t0018g0302a0001c0009t0006g0058others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.12+8853C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157832299 | ||||||
| chr6:157832527
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.12+9081A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157832527 | ||||||
| chr6:157832910
|
C | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0004g0063others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+9464C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157832910 | ||||||
| chr6:157832945
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG00544.hp1 NA18612.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+9499A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157832945 | ||||||
| chr6:157833083
|
A | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+9637A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833083 | ||||||
| chr6:157833139
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+9693A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833139 | ||||||
| chr6:157833178
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.12+9732G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833178 | ||||||
| chr6:157833309
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+9863A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833309 | ||||||
| chr6:157833353
|
A | G | 1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+9907A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833353 | ||||||
| chr6:157833596
|
G | A | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+10150G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833596 | ||||||
| chr6:157833747
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.12+10301C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157833747 | ||||||
| chr6:157834115
|
C | T | 25 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0277others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+10669C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834115 | ||||||
| chr6:157834149
|
G | GTTT | 7 | a0001c0001t0003g0257a0001c0001t0004g0063a0001c0001t0004g0065others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTT | 24 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0003g0250others(21): Show | 24 | HG00642.hp1 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTT | 12 | a0002c0002t0002g0002a0002c0002t0002g0010a0002c0002t0002g0025others(9): Show | 12 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTT | 6 | a0002c0002t0002g0016a0002c0002t0002g0018a0002c0002t0002g0023others(3): Show | 6 | HG02300.hp2 HG03654.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTTT | 3 | a0002c0002t0002g0017a0002c0002t0002g0035a0002c0002t0002g0055 | 3 | HG02083.hp2 HG02129.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.12+10703_12+10704i others(9): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTTT others(1): Show |
5 | a0002c0002t0002g0003a0002c0002t0002g0032a0002c0002t0002g0041others(2): Show | 5 | HG00423.hp1 NA18960.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTTT others(2): Show |
6 | a0002c0002t0002g0007a0002c0002t0002g0008a0002c0002t0002g0037others(3): Show | 6 | NA18963.hp2 NA18999.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+10703_12+10704i others(11): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0247a0001c0001t0001g0248a0002c0002t0002g0009 | 3 | HG00673.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.12+10703_12+10704i others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.12+10703_12+10704i others(17): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTT | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+10704_12+10708d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTT | G | 11 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0296others(8): Show | 11 | HG01081.hp2 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.12+10704_12+10709d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT | G | 16 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0003t0003g0263others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.12+10704_12+10710d others(9): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT others(2): Show |
G | 4 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0015others(1): Show | 4 | HG00438.hp2 HG00621.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+10704_12+10712d others(11): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT others(3): Show |
G | 5 | a0002c0002t0002g0011a0002c0002t0002g0012a0002c0002t0002g0019others(2): Show | 5 | HG00408.hp2 HG02056.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+10704_12+10713d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT others(4): Show |
G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+10704_12+10714d others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT others(5): Show |
G | 1 | a0001c0001t0019g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+10704_12+10715d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834149
|
GGTTTTTT others(11): Show |
G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+10704_12+10721d others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834149 | ||||||
| chr6:157834150
|
G | GT | 61 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0071others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.12+10739dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
G | GTT | 39 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0001t0001g0089others(36): Show | 39 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.12+10738_12+10739d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
G | GTTT | 21 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0079others(18): Show | 21 | HG00544.hp2 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+10737_12+10739d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
G | GTTTT | 14 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0137others(11): Show | 14 | HG01358.hp2 HG01934.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+10736_12+10739d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
G | GTTTTT | 9 | a0001c0001t0001g0104a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG01175.hp1 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.12+10735_12+10739d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
G | T | 70 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0300others(67): Show | 70 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.12+10704G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834150 | ||||||
| chr6:157834150
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0004g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12+10730_12+10739d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0015g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12+10729_12+10739d others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834150
|
GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+10728_12+10739d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834150 | |||||
| chr6:157834166
|
T | G | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+10720T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834166 | ||||||
| chr6:157834167
|
T | G | 1 | a0001c0001t0005g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.12+10721T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834167 | ||||||
| chr6:157834169
|
T | G | 9 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0294others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+10723T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834169 | ||||||
| chr6:157834170
|
T | G | 1 | a0001c0001t0005g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.12+10724T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834170 | ||||||
| chr6:157834173
|
T | G | 8 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+10727T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834173 | ||||||
| chr6:157834174
|
T | G | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+10728T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834174 | ||||||
| chr6:157834175
|
T | G | 1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.12+10729T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834175 | ||||||
| chr6:157834177
|
T | G | 7 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0294others(4): Show | 7 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+10731T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834177 | ||||||
| chr6:157834188
|
G | T | 1 | a0002c0002t0002g0017 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.12+10742G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834188 | ||||||
| chr6:157834346
|
A | AT | 61 | a0001c0001t0001g0073a0001c0001t0001g0109a0001c0001t0001g0134others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.12+10915dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834346 | |||||
| chr6:157834518
|
T | A | 2 | a0001c0001t0018g0302a0001c0003t0022g0292 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.12+11072T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834518 | ||||||
| chr6:157834521
|
A | AT | 40 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0250others(37): Show | 40 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.12+11084dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157834521 | |||||
| chr6:157834581
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.12+11135C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834581 | ||||||
| chr6:157834619
|
A | T | 299 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.12+11173A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834619 | ||||||
| chr6:157834957
|
G | T | 9 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0003t0003g0251others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+11511G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157834957 | ||||||
| chr6:157835017
|
T | A | 1 | a0002c0002t0002g0042 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.12+11571T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835017 | ||||||
| chr6:157835045
|
C | T | 71 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.12+11599C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835045 | ||||||
| chr6:157835143
|
A | G | 73 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0005g0288others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.12+11697A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835143 | ||||||
| chr6:157835169
|
C | T | 3 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.12+11723C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835169 | ||||||
| chr6:157835196
|
G | A | 111 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0003g0250others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.12+11750G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835196 | ||||||
| chr6:157835412
|
C | CT | 12 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0088others(9): Show | 12 | HG02559.hp1 HG02559.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.12+11985dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157835412 | |||||
| chr6:157835412
|
CT | C | 18 | a0001c0001t0001g0071a0001c0001t0001g0087a0001c0001t0001g0117others(15): Show | 18 | HG01257.hp1 HG01358.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+11985delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157835412 | |||||
| chr6:157835417
|
T | TTTTTTTT others(2198): Show |
1 | a0001c0001t0001g0232 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.12+11985_12+11986i others(2207): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157835417 | |||||
| chr6:157835420
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.12+11974T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835420 | ||||||
| chr6:157835577
|
A | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.12+12131A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835577 | ||||||
| chr6:157835650
|
C | T | 74 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0001t0005g0288others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.12+12204C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835650 | ||||||
| chr6:157835818
|
A | G | 9 | a0001c0001t0001g0267a0001c0001t0001g0280a0001c0003t0003g0279others(6): Show | 9 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+12372A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835818 | ||||||
| chr6:157835893
|
T | C | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+12447T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157835893 | ||||||
| chr6:157836119
|
T | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+12673T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836119 | ||||||
| chr6:157836174
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+12728T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836174 | ||||||
| chr6:157836271
|
G | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.12+12825G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836271 | ||||||
| chr6:157836548
|
T | C | 1 | a0006c0014t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.12+13102T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836548 | ||||||
| chr6:157836619
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.12+13173G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836619 | ||||||
| chr6:157836676
|
C | G | 1 | a0001c0001t0015g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12+13230C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836676 | ||||||
| chr6:157836802
|
C | A | 101 | a0001c0001t0001g0061a0001c0001t0001g0125a0001c0001t0001g0134others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.12+13356C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836802 | ||||||
| chr6:157836827
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+13381G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157836827 | ||||||
| chr6:157837129
|
C | T | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+13683C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837129 | ||||||
| chr6:157837156
|
C | A | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.12+13710C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837156 | ||||||
| chr6:157837275
|
A | G | 1 | a0001c0001t0019g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+13829A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837275 | ||||||
| chr6:157837420
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.12+13974A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837420 | ||||||
| chr6:157837513
|
A | G | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+14067A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837513 | ||||||
| chr6:157837643
|
T | G | 1 | a0001c0001t0014g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.12+14197T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837643 | ||||||
| chr6:157837780
|
G | A | 9 | a0002c0002t0002g0011a0002c0002t0002g0012a0002c0002t0002g0013others(6): Show | 9 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+14334G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837780 | ||||||
| chr6:157837826
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12+14380G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837826 | ||||||
| chr6:157837877
|
C | T | 1 | a0002c0002t0002g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.12+14431C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157837877 | ||||||
| chr6:157838112
|
G | A | 74 | a0001c0001t0001g0146a0001c0001t0003g0250a0001c0001t0003g0257others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.12+14666G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838112 | ||||||
| chr6:157838120
|
T | C | 237 | a0001c0001t0001g0061a0001c0001t0001g0125a0001c0001t0001g0134others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.12+14674T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838120 | ||||||
| chr6:157838317
|
AT | A | 20 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0158others(17): Show | 20 | HG01255.hp1 HG01256.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.12+14885delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157838317 | |||||
| chr6:157838448
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.12+15002G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838448 | ||||||
| chr6:157838453
|
G | A | 2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+15007G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838453 | ||||||
| chr6:157838558
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0245 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.12+15112A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838558 | ||||||
| chr6:157838828
|
T | C | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+15382T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838828 | ||||||
| chr6:157838998
|
T | C | 1 | a0002c0002t0002g0017 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.12+15552T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157838998 | ||||||
| chr6:157839322
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.12+15876A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839322 | ||||||
| chr6:157839345
|
A | T | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+15899A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839345 | ||||||
| chr6:157839415
|
A | C | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.12+15969A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839415 | ||||||
| chr6:157839597
|
G | A | 2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+16151G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839597 | ||||||
| chr6:157839633
|
G | A | 117 | a0001c0001t0001g0146a0001c0001t0001g0247a0001c0001t0001g0248others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.12+16187G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839633 | ||||||
| chr6:157839767
|
C | G | 1 | a0001c0001t0005g0295 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12+16321C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839767 | ||||||
| chr6:157839782
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.12+16336G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839782 | ||||||
| chr6:157839798
|
C | T | 10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0005g0288others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+16352C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839798 | ||||||
| chr6:157839927
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.12+16481T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839927 | ||||||
| chr6:157839930
|
A | G | 10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0005g0288others(7): Show | 10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.12+16484A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839930 | ||||||
| chr6:157839998
|
A | G | 4 | a0001c0003t0003g0270a0001c0003t0003g0272a0001c0003t0003g0274others(1): Show | 4 | HG02735.hp1 HG03491.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+16552A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157839998 | ||||||
| chr6:157840058
|
G | GGGGGTGT others(41): Show |
12 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0112others(9): Show | 12 | HG00408.hp1 HG02273.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.12+16758_12+16805d others(50): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840058 | |||||
| chr6:157840058
|
GGGGGTGT others(41): Show |
G | 50 | a0001c0001t0001g0077a0001c0001t0001g0092a0001c0001t0001g0096others(47): Show | 50 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.12+16758_12+16805d others(50): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840058 | |||||
| chr6:157840058
|
GGGGGTGT others(89): Show |
G | 117 | a0001c0001t0001g0061a0001c0001t0001g0147a0001c0001t0001g0157others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.12+16710_12+16805d others(98): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840058 | |||||
| chr6:157840076
|
C | CGGGAAAG others(41): Show |
1 | a0001c0001t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.12+16677_12+16678i others(50): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840076 | |||||
| chr6:157840124
|
C | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG00544.hp1 NA18612.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.12+16678C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840124 | ||||||
| chr6:157840125
|
G | A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+16679G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840125 | ||||||
| chr6:157840173
|
G | A | 2 | a0001c0001t0011g0060a0001c0001t0018g0302 | 2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.12+16727G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840173 | ||||||
| chr6:157840193
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.12+16747G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840193 | ||||||
| chr6:157840221
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12+16775G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840221 | ||||||
| chr6:157840241
|
G | A | 81 | a0001c0001t0001g0153a0001c0001t0001g0182a0001c0001t0003g0250others(78): Show | 81 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.12+16795G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840241 | ||||||
| chr6:157840261
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.12+16815G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840261 | ||||||
| chr6:157840262
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0190a0001c0001t0001g0206others(1): Show | 4 | HG01255.hp1 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+16816C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840262 | ||||||
| chr6:157840294
|
G | A | 67 | a0001c0001t0001g0228a0001c0001t0004g0260a0001c0001t0004g0261others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.12+16848G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840294 | ||||||
| chr6:157840326
|
G | A | 80 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0228others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.12+16880G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840326 | ||||||
| chr6:157840381
|
A | G | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+16935A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840381 | ||||||
| chr6:157840384
|
ATGAC | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.12+16944_12+16947d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840384 | |||||
| chr6:157840404
|
A | ATTCTTTC others(1): Show |
47 | a0001c0001t0011g0259a0001c0001t0013g0298a0002c0002t0002g0009others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.12+16959_12+16960i others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840404 | |||||
| chr6:157840406
|
A | T | 116 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0115others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.12+16960A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840406 | ||||||
| chr6:157840411
|
C | A | 27 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(24): Show | 27 | HG01256.hp1 HG01258.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.12+16965C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840411 | ||||||
| chr6:157840420
|
T | TTTCCTTT others(11): Show |
7 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0260others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+16976_12+16977i others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840420
|
T | TTTCTTTC | 11 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(8): Show | 11 | NA18939.hp1 NA18960.hp1 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.12+16976_12+16977i others(9): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840420
|
T | TTTCTTTC others(10): Show |
2 | a0001c0001t0020g0287a0001c0009t0006g0058 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.12+16976_12+16977i others(19): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840420
|
T | TTTCTTTC others(14): Show |
8 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG01934.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+16976_12+16977i others(23): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840420
|
T | TTTCTTTC others(19): Show |
14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+16976_12+16977i others(28): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840420
|
T | TTTCTTTC others(23): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.12+16976_12+16977i others(32): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840420 | |||||
| chr6:157840423
|
T | C | 103 | a0001c0001t0001g0108a0001c0001t0001g0126a0001c0001t0001g0151others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.12+16977T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840423 | ||||||
| chr6:157840429
|
T | C | 34 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(31): Show | 34 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.12+16983T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840429 | ||||||
| chr6:157840432
|
T | C | 60 | a0001c0001t0011g0259a0001c0001t0013g0298a0001c0001t0018g0302others(57): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.12+16986T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840432 | ||||||
| chr6:157840434
|
T | C | 34 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(31): Show | 34 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.12+16988T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840434 | ||||||
| chr6:157840434
|
T | TTTCCTTT others(11): Show |
20 | a0001c0001t0001g0144a0001c0001t0001g0161a0001c0001t0001g0248others(17): Show | 20 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.12+16995_12+17012d others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840434 | |||||
| chr6:157840448
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.12+17002T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840448 | ||||||
| chr6:157840452
|
C | CTTCCTTT others(7): Show |
14 | a0001c0001t0001g0247a0001c0003t0003g0263a0001c0003t0003g0264others(11): Show | 14 | HG01891.hp1 HG02602.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+17012_12+17013i others(16): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157840452 | |||||
| chr6:157840486
|
C | G | 8 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+17040C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840486 | ||||||
| chr6:157840518
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0115 | 2 | HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.12+17072T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840518 | ||||||
| chr6:157840687
|
A | G | 10 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+17241A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840687 | ||||||
| chr6:157840951
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.12+17505G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840951 | ||||||
| chr6:157840957
|
T | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+17511T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157840957 | ||||||
| chr6:157841126
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+17680G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841126 | ||||||
| chr6:157841130
|
T | C | 73 | a0001c0001t0001g0200a0001c0001t0001g0223a0001c0001t0004g0063others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.12+17684T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841130 | ||||||
| chr6:157841353
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0227 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.12+17907T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841353 | ||||||
| chr6:157841514
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.12+18068G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841514 | ||||||
| chr6:157841576
|
C | T | 4 | a0001c0003t0003g0285a0001c0003t0003g0286a0004c0005t0003g0282others(1): Show | 4 | HG00099.hp2 HG00642.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+18130C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841576 | ||||||
| chr6:157841604
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12+18158C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841604 | ||||||
| chr6:157841752
|
A | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+18306A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841752 | ||||||
| chr6:157841908
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+18462G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841908 | ||||||
| chr6:157841940
|
C | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+18494C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841940 | ||||||
| chr6:157841962
|
C | A | 2 | a0004c0005t0003g0282a0004c0005t0003g0283 | 2 | HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.12+18516C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841962 | ||||||
| chr6:157841976
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0001g0228a0001c0001t0009g0132others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+18530T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157841976 | ||||||
| chr6:157842149
|
T | C | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+18703T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842149 | ||||||
| chr6:157842197
|
A | G | 1 | a0001c0001t0015g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12+18751A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842197 | ||||||
| chr6:157842258
|
A | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+18812A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842258 | ||||||
| chr6:157842396
|
T | C | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+18950T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842396 | ||||||
| chr6:157842396
|
T | G | 1 | a0001c0003t0003g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.12+18950T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842396 | ||||||
| chr6:157842411
|
A | G | 1 | a0002c0002t0002g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.12+18965A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842411 | ||||||
| chr6:157842424
|
C | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.12+18978C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842424 | ||||||
| chr6:157842571
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.12+19125T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842571 | ||||||
| chr6:157842626
|
T | C | 71 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.12+19180T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157842626 | ||||||
| chr6:157843050
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.12+19604G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843050 | ||||||
| chr6:157843087
|
A | C | 14 | a0001c0001t0001g0215a0001c0001t0003g0250a0001c0001t0003g0257others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+19641A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843087 | ||||||
| chr6:157843228
|
A | G | 196 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(193): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.12+19782A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843228 | ||||||
| chr6:157843292
|
A | G | 2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.12+19846A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843292 | ||||||
| chr6:157843363
|
C | A | 84 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.12+19917C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843363 | ||||||
| chr6:157843386
|
GTATGT | G | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+19944_12+19948d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157843386 | |||||
| chr6:157843796
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.12+20350C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843796 | ||||||
| chr6:157843872
|
C | CT | 21 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0096others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+20446dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157843872 | |||||
| chr6:157843872
|
C | CTT | 70 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.12+20445_12+20446d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157843872 | |||||
| chr6:157843872
|
C | CTTT | 7 | a0001c0001t0004g0262a0001c0001t0011g0060a0001c0001t0018g0302others(4): Show | 7 | HG00621.hp1 HG01243.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+20444_12+20446d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157843872 | |||||
| chr6:157843911
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.12+20465A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843911 | ||||||
| chr6:157843929
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+20483C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843929 | ||||||
| chr6:157843975
|
A | G | 8 | a0001c0001t0001g0061a0001c0001t0001g0188a0001c0001t0001g0191others(5): Show | 8 | HG00735.hp2 HG01071.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+20529A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157843975 | ||||||
| chr6:157844001
|
C | A | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.12+20555C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844001 | ||||||
| chr6:157844038
|
C | T | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.12+20592C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844038 | ||||||
| chr6:157844369
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.12+20923A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844369 | ||||||
| chr6:157844400
|
TGGGTGGG others(33): Show |
T | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+20961_12+21000d others(42): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844400 | |||||
| chr6:157844409
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.12+20963G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844409 | ||||||
| chr6:157844423
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.12+20977T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844423 | ||||||
| chr6:157844547
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+21101G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844547 | ||||||
| chr6:157844587
|
G | GT | 6 | a0001c0001t0001g0146a0001c0001t0001g0213a0001c0001t0001g0280others(3): Show | 6 | HG01243.hp1 HG01515.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+21153dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(6): Show |
1 | a0002c0002t0002g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(7): Show |
7 | a0002c0002t0002g0009a0002c0002t0002g0033a0002c0002t0002g0044others(4): Show | 7 | HG00280.hp1 HG00673.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+21148_12+21149i others(16): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(8): Show |
2 | a0002c0002t0002g0045a0002c0002t0002g0046 | 2 | HG01257.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(17): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(26): Show |
1 | a0002c0002t0002g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.12+21148_12+21149i others(35): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(28): Show |
1 | a0002c0002t0002g0041 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(22): Show |
1 | a0002c0002t0002g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(31): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(27): Show |
1 | a0002c0002t0002g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(28): Show |
3 | a0002c0002t0002g0037a0002c0002t0002g0040a0002c0002t0002g0055 | 3 | HG02083.hp2 NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(29): Show |
1 | a0002c0002t0002g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(38): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(32): Show |
1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(41): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(9): Show |
3 | a0002c0002t0002g0010a0002c0002t0002g0023a0002c0002t0002g0056 | 3 | HG03688.hp1 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(18): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(33): Show |
2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(42): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(34): Show |
2 | a0002c0002t0002g0013a0002c0002t0002g0015 | 2 | HG00621.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(43): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(35): Show |
1 | a0002c0002t0002g0001 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.12+21148_12+21149i others(44): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(32): Show |
2 | a0002c0002t0002g0011a0002c0002t0002g0028 | 2 | HG00408.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(41): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(33): Show |
2 | a0002c0002t0002g0014a0002c0002t0002g0021 | 2 | HG00438.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(42): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(23): Show |
1 | a0002c0002t0002g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(32): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(26): Show |
2 | a0002c0002t0002g0002a0002c0002t0002g0004 | 2 | NA18939.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(35): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(27): Show |
1 | a0002c0002t0002g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(28): Show |
1 | a0002c0002t0002g0005 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(29): Show |
1 | a0002c0002t0002g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(38): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(30): Show |
2 | a0002c0002t0002g0029a0002c0002t0002g0042 | 2 | HG01358.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(39): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(31): Show |
1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.12+21148_12+21149i others(40): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(37): Show |
1 | a0002c0002t0002g0030 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(46): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(34): Show |
1 | a0002c0002t0002g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.12+21148_12+21149i others(43): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(35): Show |
2 | a0002c0002t0002g0006a0002c0002t0002g0012 | 2 | HG02056.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(44): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0021g0291 | 3 | HG02280.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.12+21144_12+21153d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(4): Show |
5 | a0001c0001t0003g0277a0001c0001t0003g0296a0001c0001t0005g0295others(2): Show | 5 | HG01256.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+21143_12+21153d others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0005g0294a0001c0010t0001g0059 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.12+21142_12+21153d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0003g0278 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.12+21153_12+21154i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(8): Show |
1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12+21153_12+21154i others(17): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(11): Show |
1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+21153_12+21154i others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(15): Show |
3 | a0002c0002t0002g0007a0002c0002t0002g0051a0002c0002t0002g0052 | 3 | NA19011.hp1 NA19012.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.12+21153_12+21154i others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(16): Show |
1 | a0002c0002t0002g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.12+21153_12+21154i others(25): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(18): Show |
1 | a0002c0002t0002g0003 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.12+21153_12+21154i others(27): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844587
|
G | GTTTTTTT others(27): Show |
1 | a0002c0002t0002g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.12+21153_12+21154i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844587 | |||||
| chr6:157844589
|
T | TTTTTTGT others(6): Show |
2 | a0002c0002t0002g0036a0002c0002t0002g0038 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.12+21148_12+21149i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844589 | |||||
| chr6:157844590
|
T | G | 1 | a0001c0001t0016g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.12+21144T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844590 | ||||||
| chr6:157844596
|
T | G | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+21150T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844596 | ||||||
| chr6:157844600
|
G | GT | 29 | a0001c0001t0001g0166a0001c0001t0001g0267a0001c0003t0003g0251others(26): Show | 29 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.12+21165dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157844600 | |||||
| chr6:157844600
|
G | T | 84 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.12+21154G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844600 | ||||||
| chr6:157844610
|
T | G | 1 | a0002c0002t0002g0042 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.12+21164T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844610 | ||||||
| chr6:157844655
|
G | A | 2 | a0002c0002t0002g0036a0002c0002t0002g0038 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.12+21209G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844655 | ||||||
| chr6:157844741
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.12+21295C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844741 | ||||||
| chr6:157844754
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.12+21308C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844754 | ||||||
| chr6:157844844
|
C | T | 1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.12+21398C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844844 | ||||||
| chr6:157844887
|
G | A | 29 | a0001c0001t0001g0267a0001c0003t0003g0251a0001c0003t0003g0252others(26): Show | 29 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.12+21441G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844887 | ||||||
| chr6:157844894
|
C | T | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.12+21448C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157844894 | ||||||
| chr6:157845105
|
C | CT | 109 | a0001c0001t0001g0080a0001c0001t0001g0135a0001c0001t0001g0136others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.12+21679dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157845105 | |||||
| chr6:157845105
|
CT | C | 7 | a0001c0001t0001g0087a0001c0001t0001g0162a0001c0001t0001g0187others(4): Show | 7 | HG00323.hp2 HG02273.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+21679delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157845105 | |||||
| chr6:157845233
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.12+21787C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845233 | ||||||
| chr6:157845485
|
G | T | 68 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.12+22039G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845485 | ||||||
| chr6:157845516
|
T | G | 15 | a0001c0001t0001g0267a0001c0003t0003g0251a0001c0003t0003g0252others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.13-22031T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845516 | ||||||
| chr6:157845671
|
T | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-21876T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845671 | ||||||
| chr6:157845818
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-21729T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845818 | ||||||
| chr6:157845819
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0249 | 2 | HG00621.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.13-21728G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157845819 | ||||||
| chr6:157846073
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.13-21474G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157846073 | ||||||
| chr6:157846395
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.13-21152G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157846395 | ||||||
| chr6:157846417
|
G | A | 114 | a0001c0001t0001g0267a0001c0001t0003g0250a0001c0001t0003g0257others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.13-21130G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157846417 | ||||||
| chr6:157846645
|
C | A | 4 | a0001c0004t0001g0170a0001c0004t0001g0173a0001c0004t0001g0176others(1): Show | 4 | NA18947.hp2 NA18952.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-20902C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157846645 | ||||||
| chr6:157846948
|
G | A | 1 | a0001c0001t0005g0288 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-20599G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157846948 | ||||||
| chr6:157847042
|
C | CA | 10 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0169others(7): Show | 10 | HG00558.hp2 HG02135.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-20497dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157847042 | |||||
| chr6:157847196
|
G | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0229 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.13-20351G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847196 | ||||||
| chr6:157847224
|
T | A | 1 | a0001c0003t0003g0251 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.13-20323T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847224 | ||||||
| chr6:157847233
|
G | T | 4 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-20314G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847233 | ||||||
| chr6:157847252
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.13-20295A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847252 | ||||||
| chr6:157847381
|
T | C | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13-20166T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847381 | ||||||
| chr6:157847623
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-19924A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847623 | ||||||
| chr6:157847738
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.13-19809C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157847738 | ||||||
| chr6:157848015
|
C | T | 1 | a0001c0001t0021g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.13-19532C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848015 | ||||||
| chr6:157848198
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-19349T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848198 | ||||||
| chr6:157848206
|
C | A | 26 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(23): Show | 26 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-19341C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848206 | ||||||
| chr6:157848248
|
C | T | 1 | a0001c0001t0021g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.13-19299C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848248 | ||||||
| chr6:157848249
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-19298G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848249 | ||||||
| chr6:157848384
|
G | A | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.13-19163G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848384 | ||||||
| chr6:157848423
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-19124A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848423 | ||||||
| chr6:157848562
|
A | G | 10 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0169others(7): Show | 10 | HG00558.hp2 HG02135.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-18985A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848562 | ||||||
| chr6:157848667
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-18880G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848667 | ||||||
| chr6:157848769
|
A | C | 1 | a0001c0003t0003g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.13-18778A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848769 | ||||||
| chr6:157848775
|
C | T | 11 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(8): Show | 11 | NA18939.hp1 NA18960.hp1 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-18772C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157848775 | ||||||
| chr6:157849125
|
A | G | 1 | a0001c0003t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.13-18422A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157849125 | ||||||
| chr6:157849133
|
A | G | 8 | a0002c0002t0002g0032a0002c0002t0002g0035a0002c0002t0002g0037others(5): Show | 8 | HG00423.hp1 HG02083.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-18414A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157849133 | ||||||
| chr6:157849528
|
A | G | 2 | a0002c0002t0002g0044a0002c0002t0002g0049 | 2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.13-18019A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157849528 | ||||||
| chr6:157849651
|
T | TAGAAAGT others(183): Show |
1 | a0001c0001t0001g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.13-17886_13-17885i others(192): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157849651 | |||||
| chr6:157849651
|
T | TAGAAAGT others(184): Show |
1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.13-17886_13-17885i others(193): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157849651 | |||||
| chr6:157849666
|
C | T | 1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.13-17881C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157849666 | ||||||
| chr6:157850210
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-17337G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850210 | ||||||
| chr6:157850282
|
T | C | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-17265T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850282 | ||||||
| chr6:157850398
|
G | A | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-17149G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850398 | ||||||
| chr6:157850556
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.13-16991G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850556 | ||||||
| chr6:157850699
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-16848A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850699 | ||||||
| chr6:157850874
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.13-16673C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850874 | ||||||
| chr6:157850902
|
G | A | 16 | a0001c0001t0001g0267a0001c0003t0003g0251a0001c0003t0003g0252others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.13-16645G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850902 | ||||||
| chr6:157850982
|
G | A | 2 | a0001c0001t0003g0250a0001c0001t0003g0257 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.13-16565G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157850982 | ||||||
| chr6:157851236
|
T | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-16311T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851236 | ||||||
| chr6:157851255
|
C | CA | 10 | a0001c0001t0001g0131a0001c0001t0001g0147a0001c0001t0001g0174others(7): Show | 10 | HG01106.hp2 HG03225.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-16278dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157851255 | |||||
| chr6:157851268
|
A | AC | 18 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(15): Show | 18 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.13-16279_13-16278i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851268 | ||||||
| chr6:157851268
|
A | C | 67 | a0001c0001t0004g0065a0001c0001t0004g0260a0001c0001t0004g0261others(64): Show | 67 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.13-16279A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851268 | ||||||
| chr6:157851288
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.13-16259T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851288 | ||||||
| chr6:157851459
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.13-16088A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851459 | ||||||
| chr6:157851487
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-16060A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851487 | ||||||
| chr6:157851574
|
A | G | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-15973A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851574 | ||||||
| chr6:157851685
|
G | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-15862G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851685 | ||||||
| chr6:157851739
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.13-15808G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851739 | ||||||
| chr6:157851910
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.13-15637C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851910 | ||||||
| chr6:157851942
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13-15605C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851942 | ||||||
| chr6:157851948
|
T | C | 1 | a0001c0001t0015g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.13-15599T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157851948 | ||||||
| chr6:157852355
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.13-15192A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852355 | ||||||
| chr6:157852463
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.13-15084C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852463 | ||||||
| chr6:157852579
|
TTTTTG | T | 28 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(25): Show | 28 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.13-14958_13-14954d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157852579 | |||||
| chr6:157852585
|
TTTTG | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.13-14958_13-14955d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157852585 | |||||
| chr6:157852730
|
C | T | 8 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-14817C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852730 | ||||||
| chr6:157852771
|
T | G | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-14776T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852771 | ||||||
| chr6:157852980
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13-14567T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852980 | ||||||
| chr6:157852985
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.13-14562G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157852985 | ||||||
| chr6:157853163
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.13-14384C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853163 | ||||||
| chr6:157853168
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.13-14379G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853168 | ||||||
| chr6:157853285
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.13-14262A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853285 | ||||||
| chr6:157853366
|
A | C | 69 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.13-14181A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853366 | ||||||
| chr6:157853366
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.13-14181A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853366 | ||||||
| chr6:157853791
|
TA | T | 117 | a0001c0001t0001g0240a0001c0001t0001g0247a0001c0001t0001g0248others(114): Show | 117 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.13-13744delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157853791 | |||||
| chr6:157853801
|
A | C | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.13-13746A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853801 | ||||||
| chr6:157853845
|
G | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13-13702G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853845 | ||||||
| chr6:157853969
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-13578G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853969 | ||||||
| chr6:157853975
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-13572A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157853975 | ||||||
| chr6:157854332
|
C | T | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.13-13215C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157854332 | ||||||
| chr6:157854512
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.13-13035C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157854512 | ||||||
| chr6:157854563
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13-12984A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157854563 | ||||||
| chr6:157854626
|
TC | T | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-12919delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157854626 | |||||
| chr6:157854754
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.13-12793G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157854754 | ||||||
| chr6:157854953
|
TA | T | 98 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.13-12578delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157854953 | |||||
| chr6:157854969
|
A | C | 83 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(80): Show | 83 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.13-12578A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157854969 | ||||||
| chr6:157855016
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-12531T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855016 | ||||||
| chr6:157855264
|
C | T | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-12283C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855264 | ||||||
| chr6:157855291
|
G | C | 1 | a0002c0002t0002g0006 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.13-12256G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855291 | ||||||
| chr6:157855396
|
G | C | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13-12151G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855396 | ||||||
| chr6:157855762
|
G | A | 1 | a0001c0013t0001g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.13-11785G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855762 | ||||||
| chr6:157855951
|
G | A | 38 | a0001c0001t0001g0153a0001c0001t0001g0162a0001c0001t0001g0164others(35): Show | 38 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.13-11596G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855951 | ||||||
| chr6:157855956
|
C | T | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-11591C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157855956 | ||||||
| chr6:157856091
|
G | A | 58 | a0001c0001t0001g0228a0002c0002t0002g0001a0002c0002t0002g0002others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.13-11456G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856091 | ||||||
| chr6:157856120
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.13-11427T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856120 | ||||||
| chr6:157856162
|
A | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-11385A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856162 | ||||||
| chr6:157856244
|
C | T | 1 | a0002c0002t0002g0005 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.13-11303C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856244 | ||||||
| chr6:157856575
|
G | A | 1 | a0001c0001t0004g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.13-10972G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856575 | ||||||
| chr6:157856641
|
G | A | 17 | a0001c0001t0001g0134a0001c0001t0001g0147a0001c0001t0001g0158others(14): Show | 17 | HG00099.hp1 HG00558.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.13-10906G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157856641 | ||||||
| chr6:157857146
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.13-10401A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857146 | ||||||
| chr6:157857459
|
T | A | 15 | a0001c0001t0001g0267a0001c0003t0003g0251a0001c0003t0003g0252others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.13-10088T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857459 | ||||||
| chr6:157857460
|
A | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02717.hp1 HG03139.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.13-10087A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857460 | ||||||
| chr6:157857638
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.13-9909C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857638 | ||||||
| chr6:157857651
|
GT | G | 86 | a0001c0001t0001g0247a0001c0001t0003g0250a0001c0001t0003g0257others(83): Show | 86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.13-9883delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157857651 | |||||
| chr6:157857685
|
C | T | 3 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262 | 3 | HG01243.hp1 HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.13-9862C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857685 | ||||||
| chr6:157857770
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.13-9777T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857770 | ||||||
| chr6:157857820
|
C | G | 1 | a0002c0002t0002g0021 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.13-9727C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857820 | ||||||
| chr6:157857941
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-9606T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157857941 | ||||||
| chr6:157858167
|
A | G | 1 | a0001c0001t0005g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13-9380A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858167 | ||||||
| chr6:157858224
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.13-9323C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858224 | ||||||
| chr6:157858249
|
T | G | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-9298T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858249 | ||||||
| chr6:157858250
|
CTT | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-9285_13-9284del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157858250 | |||||
| chr6:157858341
|
G | C | 3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.13-9206G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858341 | ||||||
| chr6:157858354
|
C | G | 55 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.13-9193C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858354 | ||||||
| chr6:157858393
|
C | T | 89 | a0001c0001t0001g0267a0001c0001t0003g0250a0001c0001t0003g0257others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.13-9154C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858393 | ||||||
| chr6:157858464
|
C | T | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-9083C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858464 | ||||||
| chr6:157858469
|
G | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-9078G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858469 | ||||||
| chr6:157858514
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0083 | 2 | NA18990.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.13-9033G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858514 | ||||||
| chr6:157858518
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-9029G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858518 | ||||||
| chr6:157858605
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0009g0132a0001c0001t0009g0133 | 3 | HG01255.hp1 HG01256.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.13-8942C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858605 | ||||||
| chr6:157858788
|
G | A | 3 | a0001c0001t0006g0097a0005c0008t0006g0074a0005c0008t0006g0093 | 3 | HG02080.hp1 NA18977.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.13-8759G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157858788 | ||||||
| chr6:157859197
|
A | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13-8350A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859197 | ||||||
| chr6:157859439
|
G | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-8108G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859439 | ||||||
| chr6:157859457
|
A | G | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-8090A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859457 | ||||||
| chr6:157859646
|
G | A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13-7901G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859646 | ||||||
| chr6:157859673
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.13-7874T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859673 | ||||||
| chr6:157859724
|
G | C | 1 | a0001c0003t0003g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13-7823G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859724 | ||||||
| chr6:157859739
|
T | C | 11 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0206others(8): Show | 11 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-7808T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859739 | ||||||
| chr6:157859902
|
C | CATA | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-7642_13-7640dup others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157859902 | |||||
| chr6:157859931
|
A | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.13-7616A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157859931 | ||||||
| chr6:157860066
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.13-7481A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860066 | ||||||
| chr6:157860227
|
C | T | 5 | a0001c0003t0003g0284a0001c0003t0003g0285a0001c0003t0003g0286others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-7320C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860227 | ||||||
| chr6:157860296
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.13-7251A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860296 | ||||||
| chr6:157860341
|
G | C | 4 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-7206G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860341 | ||||||
| chr6:157860400
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.13-7147G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860400 | ||||||
| chr6:157860600
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.13-6947G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157860600 | ||||||
| chr6:157861341
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0249others(1): Show | 4 | HG00621.hp2 HG01074.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-6206C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157861341 | ||||||
| chr6:157861709
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.13-5838C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157861709 | ||||||
| chr6:157861808
|
A | G | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13-5739A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157861808 | ||||||
| chr6:157861978
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13-5569C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157861978 | ||||||
| chr6:157862155
|
C | T | 1 | a0002c0002t0002g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.13-5392C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862155 | ||||||
| chr6:157862230
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.13-5317A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862230 | ||||||
| chr6:157862365
|
CTTAAG | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.13-5177_13-5173del others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157862365 | |||||
| chr6:157862500
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0121 | 2 | NA19072.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.13-5047T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862500 | ||||||
| chr6:157862541
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.13-5006C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862541 | ||||||
| chr6:157862658
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.13-4889A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862658 | ||||||
| chr6:157862877
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.13-4670C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862877 | ||||||
| chr6:157862939
|
T | C | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.13-4608T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157862939 | ||||||
| chr6:157863019
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01515.hp1 HG03831.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.13-4528G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863019 | ||||||
| chr6:157863257
|
C | A | 1 | a0001c0001t0003g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.13-4290C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863257 | ||||||
| chr6:157863340
|
G | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-4207G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863340 | ||||||
| chr6:157863425
|
T | C | 1 | a0001c0001t0006g0097 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.13-4122T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863425 | ||||||
| chr6:157863505
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.13-4042A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863505 | ||||||
| chr6:157863539
|
A | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-4008A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863539 | ||||||
| chr6:157863558
|
A | C | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-3989A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863558 | ||||||
| chr6:157863656
|
A | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.13-3891A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863656 | ||||||
| chr6:157863932
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-3615G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157863932 | ||||||
| chr6:157864139
|
G | T | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-3408G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157864139 | ||||||
| chr6:157864379
|
A | G | 13 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(10): Show | 13 | HG02056.hp2 HG02523.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.13-3168A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157864379 | ||||||
| chr6:157864590
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.13-2957C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157864590 | ||||||
| chr6:157864603
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-2944A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157864603 | ||||||
| chr6:157864982
|
T | G | 16 | a0001c0001t0001g0267a0001c0003t0003g0203a0001c0003t0003g0251others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.13-2565T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157864982 | ||||||
| chr6:157865060
|
C | A | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.13-2487C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865060 | ||||||
| chr6:157865183
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.13-2364A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865183 | ||||||
| chr6:157865194
|
C | T | 7 | a0002c0002t0002g0032a0002c0002t0002g0035a0002c0002t0002g0037others(4): Show | 7 | HG00423.hp1 HG02083.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-2353C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865194 | ||||||
| chr6:157865340
|
G | GA | 55 | a0001c0001t0001g0091a0001c0001t0001g0112a0001c0001t0001g0116others(52): Show | 55 | HG00423.hp2 HG00642.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.13-2188dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157865340 | |||||
| chr6:157865340
|
GA | G | 7 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0222others(4): Show | 7 | HG01071.hp1 HG03688.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-2188delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157865340 | |||||
| chr6:157865353
|
A | C | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.13-2194A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865353 | ||||||
| chr6:157865429
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.13-2118C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865429 | ||||||
| chr6:157865454
|
AG | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-2089delG | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157865454 | |||||
| chr6:157865500
|
C | T | 58 | a0001c0001t0018g0302a0002c0002t0002g0001a0002c0002t0002g0002others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.13-2047C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865500 | ||||||
| chr6:157865568
|
A | G | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-1979A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865568 | ||||||
| chr6:157865619
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0246 | 2 | HG02523.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.13-1928G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865619 | ||||||
| chr6:157865663
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.13-1884G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865663 | ||||||
| chr6:157865852
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-1695G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865852 | ||||||
| chr6:157865905
|
CCT | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-1641_13-1640del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865905 | ||||||
| chr6:157865954
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.13-1593A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157865954 | ||||||
| chr6:157866023
|
G | A | 12 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-1524G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866023 | ||||||
| chr6:157866043
|
CACTT | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.13-1502_13-1499del others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157866043 | |||||
| chr6:157866154
|
A | G | 1 | a0002c0002t0002g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.13-1393A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866154 | ||||||
| chr6:157866201
|
A | G | 1 | a0001c0003t0003g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.13-1346A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866201 | ||||||
| chr6:157866320
|
A | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-1227A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866320 | ||||||
| chr6:157866504
|
G | T | 59 | a0001c0009t0006g0058a0001c0010t0001g0059a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.13-1043G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866504 | ||||||
| chr6:157866507
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.13-1040G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866507 | ||||||
| chr6:157866516
|
T | G | 115 | a0001c0001t0001g0267a0001c0001t0003g0250a0001c0001t0003g0257others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.13-1031T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866516 | ||||||
| chr6:157866550
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13-997G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866550 | ||||||
| chr6:157866654
|
C | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG00323.hp2 HG01175.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-893C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866654 | ||||||
| chr6:157866732
|
A | C | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-815A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866732 | ||||||
| chr6:157866745
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0246 | 2 | HG02523.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.13-802T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866745 | ||||||
| chr6:157866817
|
C | T | 7 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-730C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866817 | ||||||
| chr6:157866818
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13-729G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866818 | ||||||
| chr6:157866995
|
C | T | 1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.13-552C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157866995 | ||||||
| chr6:157867195
|
C | T | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.13-352C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157867195 | ||||||
| chr6:157867288
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.13-259T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157867288 | ||||||
| chr6:157867359
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.13-188C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157867359 | ||||||
| chr6:157867427
|
A | G | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-120A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157867427 | ||||||
| chr6:157867442
|
A | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-105A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | chr6 | 157867442 | ||||||
| chr6:157867473
|
A | AACTGT | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.13-71_13-67dupTGTA others(1): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 157867473 | |||||
| chr6:157867624
|
CACAAATC others(53): Show |
C | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+53_99+112delCAA others(57): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157867624 | |||||
| chr6:157867653
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.99+20G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157867653 | ||||||
| chr6:157867713
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+80G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157867713 | ||||||
| chr6:157867752
|
A | T | 1 | a0001c0001t0004g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+119A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157867752 | ||||||
| chr6:157867930
|
C | T | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.99+297C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157867930 | ||||||
| chr6:157868237
|
C | A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+604C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868237 | ||||||
| chr6:157868291
|
G | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+658G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868291 | ||||||
| chr6:157868514
|
G | C | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(13): Show | 16 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+881G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868514 | ||||||
| chr6:157868554
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.99+921A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868554 | ||||||
| chr6:157868645
|
G | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.99+1012G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868645 | ||||||
| chr6:157868699
|
A | G | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(13): Show | 16 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+1066A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868699 | ||||||
| chr6:157868767
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.99+1134T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868767 | ||||||
| chr6:157868770
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+1137A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868770 | ||||||
| chr6:157868820
|
T | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+1187T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868820 | ||||||
| chr6:157868912
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+1279C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157868912 | ||||||
| chr6:157869033
|
T | C | 1 | a0001c0003t0003g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+1400T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869033 | ||||||
| chr6:157869078
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.99+1445C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869078 | ||||||
| chr6:157869086
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+1453C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869086 | ||||||
| chr6:157869136
|
T | C | 277 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.99+1503T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869136 | ||||||
| chr6:157869470
|
T | C | 114 | a0001c0001t0001g0267a0001c0001t0003g0250a0001c0001t0003g0257others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.99+1837T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869470 | ||||||
| chr6:157869551
|
C | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+1918C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869551 | ||||||
| chr6:157869574
|
C | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.99+1941C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869574 | ||||||
| chr6:157869575
|
T | C | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+1942T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869575 | ||||||
| chr6:157869591
|
G | A | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+1958G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869591 | ||||||
| chr6:157869648
|
G | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.99+2015G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869648 | ||||||
| chr6:157869693
|
T | C | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.99+2060T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869693 | ||||||
| chr6:157869848
|
C | T | 1 | a0001c0003t0003g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+2215C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157869848 | ||||||
| chr6:157869851
|
CCA | C | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2226_99+2227del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157869851 | |||||
| chr6:157870096
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+2463C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870096 | ||||||
| chr6:157870237
|
C | T | 1 | a0001c0001t0010g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.99+2604C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870237 | ||||||
| chr6:157870252
|
GCT | G | 5 | a0001c0001t0001g0157a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG00323.hp2 HG01175.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2625_99+2626del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157870252 | |||||
| chr6:157870318
|
ACT | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099 | 3 | HG00558.hp1 HG02135.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.99+2691_99+2692del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157870318 | |||||
| chr6:157870421
|
C | T | 2 | a0002c0002t0002g0041a0002c0002t0002g0044 | 2 | HG00280.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.100-2681C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870421 | ||||||
| chr6:157870422
|
G | A | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2680G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870422 | ||||||
| chr6:157870431
|
C | T | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | NA18977.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.100-2671C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870431 | ||||||
| chr6:157870463
|
G | C | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100-2639G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870463 | ||||||
| chr6:157870525
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-2577C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870525 | ||||||
| chr6:157870559
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-2543T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870559 | ||||||
| chr6:157870638
|
T | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2464T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870638 | ||||||
| chr6:157870770
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.100-2332C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870770 | ||||||
| chr6:157870889
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-2213G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870889 | ||||||
| chr6:157870949
|
C | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2153C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157870949 | ||||||
| chr6:157871084
|
T | C | 16 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(13): Show | 16 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-2018T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157871084 | ||||||
| chr6:157871191
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-1911G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157871191 | ||||||
| chr6:157871418
|
A | G | 1 | a0006c0014t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.100-1684A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157871418 | ||||||
| chr6:157871773
|
CT | C | 16 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0003t0003g0251others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-1309delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157871773 | |||||
| chr6:157871773
|
CTT | C | 68 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.100-1310_100-1309d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157871773 | |||||
| chr6:157871773
|
CTTT | C | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-1311_100-1309d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 157871773 | |||||
| chr6:157871832
|
G | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.100-1270G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157871832 | ||||||
| chr6:157872145
|
G | C | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.100-957G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872145 | ||||||
| chr6:157872259
|
C | A | 1 | a0001c0012t0001g0202 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.100-843C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872259 | ||||||
| chr6:157872370
|
A | G | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100-732A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872370 | ||||||
| chr6:157872541
|
T | C | 71 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.100-561T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872541 | ||||||
| chr6:157872541
|
T | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100-561T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872541 | ||||||
| chr6:157872581
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-521G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872581 | ||||||
| chr6:157872613
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-489A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872613 | ||||||
| chr6:157872690
|
G | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.100-412G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872690 | ||||||
| chr6:157872737
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.100-365G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872737 | ||||||
| chr6:157872820
|
G | A | 2 | a0001c0009t0006g0058a0001c0010t0001g0059 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.100-282G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872820 | ||||||
| chr6:157872845
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-257G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872845 | ||||||
| chr6:157872852
|
C | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-250C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157872852 | ||||||
| chr6:157873043
|
C | G | 1 | a0001c0011t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-59C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 2/17 | chr6 | 157873043 | ||||||
| chr6:157873329
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.174+153A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873329 | ||||||
| chr6:157873388
|
G | A | 114 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(111): Show | 114 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.174+212G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873388 | ||||||
| chr6:157873472
|
C | CTATATTA others(6): Show |
11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+309_174+321dup others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 157873472 | |||||
| chr6:157873539
|
ATC | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.174+365_174+366del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 157873539 | |||||
| chr6:157873588
|
AAT | A | 85 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.174+418_174+419del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 157873588 | |||||
| chr6:157873626
|
A | G | 56 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174+450A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873626 | ||||||
| chr6:157873708
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.174+532T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873708 | ||||||
| chr6:157873708
|
T | C | 45 | a0001c0001t0001g0121a0001c0001t0001g0146a0001c0001t0001g0153others(42): Show | 45 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.174+532T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873708 | ||||||
| chr6:157873712
|
T | G | 2 | a0002c0002t0002g0010a0002c0002t0002g0023 | 2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.174+536T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873712 | ||||||
| chr6:157873827
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.174+651G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873827 | ||||||
| chr6:157873846
|
A | G | 113 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.174+670A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873846 | ||||||
| chr6:157873882
|
C | T | 1 | a0001c0001t0019g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.174+706C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873882 | ||||||
| chr6:157873920
|
G | A | 1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.174+744G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873920 | ||||||
| chr6:157873955
|
G | A | 2 | a0001c0001t0001g0119a0003c0006t0001g0120 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+779G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157873955 | ||||||
| chr6:157874302
|
T | C | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.175-749T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874302 | ||||||
| chr6:157874455
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0244 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.175-596T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874455 | ||||||
| chr6:157874456
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.175-595T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874456 | ||||||
| chr6:157874586
|
G | A | 1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.175-465G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874586 | ||||||
| chr6:157874658
|
T | C | 116 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0267others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.175-393T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874658 | ||||||
| chr6:157874668
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.175-383C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874668 | ||||||
| chr6:157874990
|
C | G | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.175-61C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874990 | ||||||
| chr6:157874991
|
G | A | 1 | a0001c0003t0022g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175-60G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 3/17 | chr6 | 157874991 | ||||||
| chr6:157875229
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.300+53G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875229 | ||||||
| chr6:157875291
|
C | T | 9 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270others(6): Show | 9 | HG02602.hp1 HG02735.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.300+115C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875291 | ||||||
| chr6:157875398
|
T | TATTA | 84 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.300+225_300+226ins others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157875398 | |||||
| chr6:157875489
|
G | C | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+313G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875489 | ||||||
| chr6:157875611
|
C | T | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.300+435C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875611 | ||||||
| chr6:157875639
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.300+463A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875639 | ||||||
| chr6:157875980
|
G | A | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300+804G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157875980 | ||||||
| chr6:157876071
|
A | AT | 14 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(11): Show | 14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+905dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157876071 | |||||
| chr6:157876508
|
C | T | 14 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(11): Show | 14 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+1332C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876508 | ||||||
| chr6:157876555
|
T | C | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+1379T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876555 | ||||||
| chr6:157876585
|
A | AT | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02895.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.300+1412dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157876585 | |||||
| chr6:157876745
|
A | C | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.300+1569A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876745 | ||||||
| chr6:157876768
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.300+1592C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876768 | ||||||
| chr6:157876900
|
A | G | 1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.300+1724A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876900 | ||||||
| chr6:157876936
|
T | C | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+1760T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157876936 | ||||||
| chr6:157877109
|
C | T | 4 | a0002c0002t0002g0025a0002c0002t0002g0026a0002c0002t0002g0027others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+1933C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877109 | ||||||
| chr6:157877111
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.300+1935A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877111 | ||||||
| chr6:157877122
|
G | A | 84 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.300+1946G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877122 | ||||||
| chr6:157877281
|
C | CG | 41 | a0001c0001t0001g0180a0001c0001t0001g0217a0001c0001t0001g0227others(38): Show | 41 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.300+2113dupG | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157877281 | |||||
| chr6:157877296
|
G | T | 56 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.300+2120G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877296 | ||||||
| chr6:157877438
|
A | G | 7 | a0001c0003t0003g0279a0001c0003t0003g0281a0001c0003t0003g0284others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2262A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877438 | ||||||
| chr6:157877611
|
G | A | 4 | a0002c0002t0002g0025a0002c0002t0002g0026a0002c0002t0002g0027others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+2435G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877611 | ||||||
| chr6:157877617
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.300+2441G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877617 | ||||||
| chr6:157877909
|
G | T | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2733G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877909 | ||||||
| chr6:157877913
|
C | A | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+2737C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877913 | ||||||
| chr6:157877917
|
T | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2741T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157877917 | ||||||
| chr6:157878138
|
A | T | 1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.300+2962A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878138 | ||||||
| chr6:157878391
|
A | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+3215A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878391 | ||||||
| chr6:157878430
|
C | CT | 14 | a0001c0001t0003g0257a0001c0001t0003g0277a0001c0001t0003g0278others(11): Show | 14 | HG01175.hp2 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.300+3254_300+3255i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878430 | ||||||
| chr6:157878430
|
CAT | C | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.300+3255_300+3256d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878430 | ||||||
| chr6:157878431
|
A | AT | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.300+3271dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157878431 | |||||
| chr6:157878431
|
A | T | 56 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(53): Show | 56 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.300+3255A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878431 | ||||||
| chr6:157878460
|
C | T | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+3284C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878460 | ||||||
| chr6:157878461
|
G | A | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+3285G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878461 | ||||||
| chr6:157878468
|
C | T | 57 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.300+3292C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878468 | ||||||
| chr6:157878618
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.300+3442A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878618 | ||||||
| chr6:157878692
|
A | G | 1 | a0002c0002t0002g0025 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.300+3516A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878692 | ||||||
| chr6:157878813
|
C | T | 1 | a0001c0003t0003g0285 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.300+3637C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878813 | ||||||
| chr6:157878868
|
A | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.300+3692A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878868 | ||||||
| chr6:157878889
|
G | GA | 70 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.300+3718dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157878889 | |||||
| chr6:157878920
|
C | T | 70 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.300+3744C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878920 | ||||||
| chr6:157878926
|
GT | G | 99 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.300+3751delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878926 | ||||||
| chr6:157878927
|
T | G | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+3751T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878927 | ||||||
| chr6:157878936
|
G | A | 28 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+3760G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157878936 | ||||||
| chr6:157879178
|
C | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+4002C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879178 | ||||||
| chr6:157879252
|
G | A | 1 | a0001c0003t0003g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.300+4076G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879252 | ||||||
| chr6:157879330
|
G | C | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+4154G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879330 | ||||||
| chr6:157879515
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.300+4339A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879515 | ||||||
| chr6:157879700
|
A | G | 12 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.300+4524A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879700 | ||||||
| chr6:157879738
|
T | A | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.300+4562T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879738 | ||||||
| chr6:157879842
|
C | T | 1 | a0004c0005t0003g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.300+4666C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157879842 | ||||||
| chr6:157880103
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.300+4927G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157880103 | ||||||
| chr6:157880298
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.300+5122T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157880298 | ||||||
| chr6:157880391
|
C | T | 28 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+5215C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157880391 | ||||||
| chr6:157880764
|
C | G | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300+5588C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157880764 | ||||||
| chr6:157881262
|
A | G | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.300+6086A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157881262 | ||||||
| chr6:157881323
|
C | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+6147C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157881323 | ||||||
| chr6:157881337
|
G | A | 84 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(81): Show | 84 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.300+6161G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157881337 | ||||||
| chr6:157881713
|
G | T | 54 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.300+6537G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157881713 | ||||||
| chr6:157882138
|
G | A | 7 | a0002c0002t0002g0032a0002c0002t0002g0035a0002c0002t0002g0037others(4): Show | 7 | HG00423.hp1 HG02083.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+6962G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882138 | ||||||
| chr6:157882423
|
T | G | 116 | a0001c0001t0001g0169a0001c0001t0001g0245a0001c0001t0001g0267others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.300+7247T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882423 | ||||||
| chr6:157882485
|
C | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+7309C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882485 | ||||||
| chr6:157882556
|
G | A | 25 | a0001c0001t0001g0061a0001c0001t0001g0149a0001c0001t0001g0150others(22): Show | 25 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.300+7380G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882556 | ||||||
| chr6:157882679
|
A | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | HG02145.hp2 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+7503A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882679 | ||||||
| chr6:157882831
|
G | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.300+7655G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157882831 | ||||||
| chr6:157883051
|
A | G | 94 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0121others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.300+7875A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883051 | ||||||
| chr6:157883086
|
A | G | 2 | a0001c0003t0003g0268a0001c0003t0003g0269 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.300+7910A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883086 | ||||||
| chr6:157883154
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.300+7978G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883154 | ||||||
| chr6:157883237
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300+8061T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883237 | ||||||
| chr6:157883300
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.300+8124A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883300 | ||||||
| chr6:157883473
|
T | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.300+8297T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883473 | ||||||
| chr6:157883587
|
T | C | 4 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0011g0060others(1): Show | 4 | HG02622.hp1 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+8411T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883587 | ||||||
| chr6:157883606
|
A | G | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(9): Show | 12 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+8430A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883606 | ||||||
| chr6:157883619
|
C | A | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.300+8443C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883619 | ||||||
| chr6:157883620
|
T | C | 2 | a0002c0002t0008g0022a0002c0002t0008g0024 | 2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.300+8444T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883620 | ||||||
| chr6:157883657
|
T | C | 1 | a0001c0001t0005g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.300+8481T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883657 | ||||||
| chr6:157883745
|
C | G | 2 | a0001c0001t0003g0250a0001c0001t0003g0257 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.300+8569C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883745 | ||||||
| chr6:157883883
|
A | G | 27 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.300+8707A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157883883 | ||||||
| chr6:157884039
|
T | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+8863T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884039 | ||||||
| chr6:157884088
|
G | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.300+8912G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884088 | ||||||
| chr6:157884133
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.300+8957G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884133 | ||||||
| chr6:157884253
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.300+9077C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884253 | ||||||
| chr6:157884281
|
AATTAT | A | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.300+9109_300+9113d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157884281 | |||||
| chr6:157884384
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.300+9208A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884384 | ||||||
| chr6:157884605
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18939.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.300+9429G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884605 | ||||||
| chr6:157884705
|
T | C | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.300+9529T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884705 | ||||||
| chr6:157884766
|
T | A | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300+9590T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884766 | ||||||
| chr6:157884922
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.300+9746C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884922 | ||||||
| chr6:157884979
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.300+9803T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157884979 | ||||||
| chr6:157885055
|
T | G | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.300+9879T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885055 | ||||||
| chr6:157885064
|
A | G | 32 | a0001c0001t0001g0267a0001c0003t0003g0203a0001c0003t0003g0251others(29): Show | 32 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.300+9888A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885064 | ||||||
| chr6:157885343
|
C | T | 16 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.300+10167C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885343 | ||||||
| chr6:157885601
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18942.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.300+10425C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885601 | ||||||
| chr6:157885656
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0201 | 2 | HG00597.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.300+10480G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885656 | ||||||
| chr6:157885728
|
A | G | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+10552A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885728 | ||||||
| chr6:157885887
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300+10711C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157885887 | ||||||
| chr6:157886009
|
C | T | 4 | a0001c0001t0001g0216a0001c0001t0004g0260a0001c0001t0004g0261others(1): Show | 4 | HG01071.hp1 HG01243.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-10818C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157886009 | ||||||
| chr6:157886517
|
G | A | 111 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.301-10310G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157886517 | ||||||
| chr6:157886683
|
C | T | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.301-10144C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157886683 | ||||||
| chr6:157886728
|
C | A | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-10099C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157886728 | ||||||
| chr6:157886970
|
A | G | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.301-9857A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157886970 | ||||||
| chr6:157887606
|
G | A | 12 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-9221G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157887606 | ||||||
| chr6:157887610
|
C | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-9217C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157887610 | ||||||
| chr6:157887801
|
C | T | 5 | a0001c0001t0001g0157a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG00323.hp2 HG01175.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-9026C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157887801 | ||||||
| chr6:157887965
|
A | G | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.301-8862A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157887965 | ||||||
| chr6:157888009
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.301-8818G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157888009 | ||||||
| chr6:157888059
|
T | TTGGCCTT others(6): Show |
2 | a0002c0002t0002g0041a0002c0002t0002g0057 | 2 | NA18987.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.301-8766_301-8765i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157888059 | |||||
| chr6:157888059
|
T | TTGGCCTT others(6): Show |
78 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(75): Show | 78 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.301-8766_301-8765i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157888059 | |||||
| chr6:157888098
|
G | A | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.301-8729G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157888098 | ||||||
| chr6:157888634
|
TCTC | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-8190_301-8188d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157888634 | |||||
| chr6:157888928
|
T | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-7899T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157888928 | ||||||
| chr6:157889028
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0227 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.301-7799C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889028 | ||||||
| chr6:157889090
|
A | C | 1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.301-7737A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889090 | ||||||
| chr6:157889166
|
C | T | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.301-7661C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889166 | ||||||
| chr6:157889228
|
C | T | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.301-7599C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889228 | ||||||
| chr6:157889430
|
C | CA | 63 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0099others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.301-7376dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157889430 | |||||
| chr6:157889562
|
T | C | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-7265T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889562 | ||||||
| chr6:157889693
|
T | C | 1 | a0002c0002t0002g0014 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.301-7134T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889693 | ||||||
| chr6:157889758
|
G | A | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.301-7069G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889758 | ||||||
| chr6:157889822
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.301-7005G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889822 | ||||||
| chr6:157889887
|
A | C | 32 | a0001c0001t0001g0267a0001c0003t0003g0203a0001c0003t0003g0251others(29): Show | 32 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.301-6940A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889887 | ||||||
| chr6:157889970
|
G | T | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.301-6857G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889970 | ||||||
| chr6:157889989
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.301-6838A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157889989 | ||||||
| chr6:157890067
|
A | G | 10 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0172others(7): Show | 10 | HG00544.hp2 NA18747.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-6760A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890067 | ||||||
| chr6:157890082
|
A | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0245a0002c0002t0008g0022others(1): Show | 4 | HG00733.hp2 HG00735.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-6745A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890082 | ||||||
| chr6:157890113
|
A | C | 68 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.301-6714A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890113 | ||||||
| chr6:157890165
|
C | T | 1 | a0002c0002t0002g0026 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.301-6662C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890165 | ||||||
| chr6:157890193
|
A | G | 1 | a0001c0003t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.301-6634A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890193 | ||||||
| chr6:157890193
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.301-6634A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890193 | ||||||
| chr6:157890242
|
T | C | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-6585T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890242 | ||||||
| chr6:157890435
|
T | G | 1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301-6392T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890435 | ||||||
| chr6:157890444
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.301-6383G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890444 | ||||||
| chr6:157890467
|
C | T | 14 | a0001c0001t0001g0123a0001c0003t0003g0263a0001c0003t0003g0264others(11): Show | 14 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-6360C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890467 | ||||||
| chr6:157890588
|
T | G | 2 | a0002c0002t0002g0044a0002c0002t0002g0049 | 2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.301-6239T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890588 | ||||||
| chr6:157890658
|
A | G | 18 | a0001c0001t0001g0267a0001c0003t0003g0203a0001c0003t0003g0251others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.301-6169A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890658 | ||||||
| chr6:157890753
|
A | G | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-6074A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890753 | ||||||
| chr6:157890757
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.301-6070G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890757 | ||||||
| chr6:157890761
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-6066G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890761 | ||||||
| chr6:157890917
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.301-5910C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890917 | ||||||
| chr6:157890982
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301-5845A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157890982 | ||||||
| chr6:157891001
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01515.hp1 HG03831.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.301-5826C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891001 | ||||||
| chr6:157891027
|
C | CT | 18 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0113others(15): Show | 18 | HG00438.hp1 HG01243.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.301-5778dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157891027 | |||||
| chr6:157891027
|
C | CTTTT | 46 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(43): Show | 46 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.301-5781_301-5778d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157891027 | |||||
| chr6:157891027
|
C | CTTTTT | 7 | a0001c0009t0006g0058a0002c0002t0002g0004a0002c0002t0002g0016others(4): Show | 7 | HG00423.hp1 HG01928.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-5782_301-5778d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157891027 | |||||
| chr6:157891027
|
CT | C | 15 | a0001c0001t0001g0130a0001c0001t0001g0168a0001c0001t0001g0218others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.301-5778delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157891027 | |||||
| chr6:157891027
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0222 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.301-5787_301-5778d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157891027 | |||||
| chr6:157891028
|
T | TC | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-5799_301-5798i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891028 | ||||||
| chr6:157891085
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-5742G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891085 | ||||||
| chr6:157891100
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.301-5727C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891100 | ||||||
| chr6:157891249
|
A | G | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-5578A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891249 | ||||||
| chr6:157891345
|
G | A | 1 | a0001c0001t0003g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.301-5482G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891345 | ||||||
| chr6:157891479
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.301-5348C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891479 | ||||||
| chr6:157891628
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301-5199A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891628 | ||||||
| chr6:157891751
|
G | A | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-5076G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891751 | ||||||
| chr6:157891792
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0110 | 2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.301-5035G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157891792 | ||||||
| chr6:157892040
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0223 | 2 | HG02523.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.301-4787G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892040 | ||||||
| chr6:157892046
|
T | TAAG | 80 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(77): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.301-4779_301-4777d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157892046 | |||||
| chr6:157892377
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.301-4450G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892377 | ||||||
| chr6:157892389
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.301-4438G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892389 | ||||||
| chr6:157892467
|
C | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.301-4360C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892467 | ||||||
| chr6:157892501
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.301-4326T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892501 | ||||||
| chr6:157892530
|
T | C | 1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.301-4297T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892530 | ||||||
| chr6:157892573
|
A | G | 9 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-4254A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892573 | ||||||
| chr6:157892625
|
A | G | 1 | a0001c0003t0003g0285 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.301-4202A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892625 | ||||||
| chr6:157892884
|
C | T | 33 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(30): Show | 33 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.301-3943C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892884 | ||||||
| chr6:157892888
|
G | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-3939G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157892888 | ||||||
| chr6:157892961
|
GC | G | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.301-3862delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157892961 | |||||
| chr6:157893029
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.301-3798C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893029 | ||||||
| chr6:157893226
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-3601G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893226 | ||||||
| chr6:157893299
|
C | G | 9 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270others(6): Show | 9 | HG02602.hp1 HG02735.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.301-3528C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893299 | ||||||
| chr6:157893366
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.301-3461A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893366 | ||||||
| chr6:157893379
|
G | A | 6 | a0001c0001t0001g0147a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-3448G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893379 | ||||||
| chr6:157893454
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301-3373C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893454 | ||||||
| chr6:157893478
|
T | C | 12 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.301-3349T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893478 | ||||||
| chr6:157893519
|
GTGTC | G | 43 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(40): Show | 43 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.301-3303_301-3300d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893519 | |||||
| chr6:157893576
|
T | A | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.301-3251T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893576 | ||||||
| chr6:157893582
|
T | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-3245T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893582 | ||||||
| chr6:157893599
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.301-3228T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893599 | ||||||
| chr6:157893608
|
T | TG | 6 | a0001c0001t0001g0089a0001c0001t0001g0102a0001c0001t0001g0182others(3): Show | 6 | HG00323.hp2 HG01071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-3219_301-3218i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893608 | ||||||
| chr6:157893608
|
T | TTG | 176 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(173): Show | 176 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.301-3195_301-3194d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893608 | |||||
| chr6:157893608
|
T | TTGTG | 23 | a0001c0001t0001g0190a0001c0001t0001g0215a0001c0001t0004g0260others(20): Show | 23 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.301-3197_301-3194d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893608 | |||||
| chr6:157893608
|
T | TTGTGTG | 9 | a0001c0001t0011g0259a0001c0003t0003g0266a0001c0003t0003g0268others(6): Show | 9 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-3199_301-3194d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893608 | |||||
| chr6:157893608
|
T | TTGTGTGT others(1): Show |
5 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-3201_301-3194d others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893608 | |||||
| chr6:157893608
|
TTG | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(2): Show | 5 | HG01346.hp2 HG01361.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-3195_301-3194d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157893608 | |||||
| chr6:157893701
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-3126G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893701 | ||||||
| chr6:157893934
|
T | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-2893T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893934 | ||||||
| chr6:157893940
|
A | G | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.301-2887A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157893940 | ||||||
| chr6:157894043
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.301-2784G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894043 | ||||||
| chr6:157894074
|
G | A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.301-2753G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894074 | ||||||
| chr6:157894079
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.301-2748A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894079 | ||||||
| chr6:157894106
|
C | CT | 14 | a0001c0001t0001g0073a0001c0001t0001g0103a0001c0001t0001g0113others(11): Show | 14 | HG00438.hp1 HG00733.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.301-2700dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894106 | |||||
| chr6:157894106
|
C | CTTTTCTT others(4): Show |
1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.301-2717_301-2716i others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894106 | |||||
| chr6:157894106
|
C | CTTTTCTT others(3): Show |
1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301-2717_301-2716i others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894106 | |||||
| chr6:157894106
|
C | CTTTTTT | 26 | a0001c0001t0013g0298a0001c0003t0003g0203a0001c0003t0003g0251others(23): Show | 26 | HG00099.hp2 HG01074.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.301-2705_301-2700d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894106 | |||||
| chr6:157894106
|
CTTT | C | 65 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.301-2702_301-2700d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894106 | |||||
| chr6:157894111
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.301-2716T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894111 | ||||||
| chr6:157894161
|
G | A | 9 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-2666G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894161 | ||||||
| chr6:157894165
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-2662A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894165 | ||||||
| chr6:157894195
|
C | T | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.301-2632C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894195 | ||||||
| chr6:157894323
|
T | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-2504T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894323 | ||||||
| chr6:157894362
|
G | A | 3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.301-2465G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894362 | ||||||
| chr6:157894368
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-2459C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894368 | ||||||
| chr6:157894376
|
G | C | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.301-2451G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894376 | ||||||
| chr6:157894413
|
A | G | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.301-2414A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894413 | ||||||
| chr6:157894443
|
G | A | 22 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(19): Show | 22 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.301-2384G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894443 | ||||||
| chr6:157894465
|
T | TA | 60 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0242others(57): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.301-2341dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894465 | |||||
| chr6:157894465
|
T | TAA | 30 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(27): Show | 30 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.301-2342_301-2341d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894465 | |||||
| chr6:157894465
|
TA | T | 7 | a0001c0001t0001g0101a0001c0001t0001g0113a0001c0001t0001g0128others(4): Show | 7 | HG02300.hp1 HG02630.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-2341delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894465 | |||||
| chr6:157894491
|
A | T | 4 | a0001c0004t0001g0170a0001c0004t0001g0173a0001c0004t0001g0176others(1): Show | 4 | NA18947.hp2 NA18952.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.301-2336A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894491 | ||||||
| chr6:157894650
|
A | G | 1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.301-2177A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894650 | ||||||
| chr6:157894666
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.301-2161G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894666 | ||||||
| chr6:157894726
|
G | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.301-2101G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894726 | ||||||
| chr6:157894942
|
GGAAGAGA others(24): Show |
G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-1880_301-1850d others(33): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157894942 | |||||
| chr6:157894976
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-1851A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157894976 | ||||||
| chr6:157895021
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.301-1806G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895021 | ||||||
| chr6:157895108
|
A | G | 6 | a0001c0001t0001g0147a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.301-1719A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895108 | ||||||
| chr6:157895121
|
T | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.301-1706T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895121 | ||||||
| chr6:157895122
|
T | G | 9 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-1705T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895122 | ||||||
| chr6:157895434
|
A | G | 102 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.301-1393A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895434 | ||||||
| chr6:157895580
|
C | T | 91 | a0001c0001t0004g0065a0001c0001t0011g0060a0001c0001t0011g0259others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.301-1247C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895580 | ||||||
| chr6:157895664
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.301-1163G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157895664 | ||||||
| chr6:157896063
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.301-764G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896063 | ||||||
| chr6:157896100
|
T | C | 101 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.301-727T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896100 | ||||||
| chr6:157896125
|
A | G | 2 | a0002c0002t0002g0035a0002c0002t0002g0053 | 2 | NA19001.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.301-702A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896125 | ||||||
| chr6:157896427
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.301-400A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896427 | ||||||
| chr6:157896511
|
A | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301-316A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896511 | ||||||
| chr6:157896714
|
TATTA | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.301-109_301-106del others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 157896714 | |||||
| chr6:157896720
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.301-107T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896720 | ||||||
| chr6:157896799
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.301-28T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 4/17 | chr6 | 157896799 | ||||||
| chr6:157897034
|
C | T | 1 | a0002c0002t0002g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.472+36C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897034 | ||||||
| chr6:157897106
|
A | G | 55 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.472+108A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897106 | ||||||
| chr6:157897191
|
C | CATG | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.472+195_472+197dup others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157897191 | |||||
| chr6:157897371
|
C | T | 31 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(28): Show | 31 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.472+373C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897371 | ||||||
| chr6:157897389
|
C | T | 1 | a0001c0001t0010g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.472+391C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897389 | ||||||
| chr6:157897479
|
G | A | 3 | a0002c0002t0002g0003a0002c0002t0002g0007a0002c0002t0002g0008 | 3 | NA18960.hp1 NA19079.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.472+481G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897479 | ||||||
| chr6:157897501
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.472+503C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897501 | ||||||
| chr6:157897716
|
A | G | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.472+718A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157897716 | ||||||
| chr6:157898293
|
A | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18942.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.472+1295A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898293 | ||||||
| chr6:157898319
|
T | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0113others(5): Show | 8 | HG00733.hp1 HG01081.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+1321T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898319 | ||||||
| chr6:157898510
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.472+1512T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898510 | ||||||
| chr6:157898550
|
TC | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(1): Show | 4 | HG02523.hp2 NA18947.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+1554delC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157898550 | |||||
| chr6:157898658
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+1660G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898658 | ||||||
| chr6:157898706
|
T | C | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.472+1708T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898706 | ||||||
| chr6:157898728
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.472+1730T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898728 | ||||||
| chr6:157898769
|
T | C | 6 | a0002c0002t0002g0044a0002c0002t0002g0045a0002c0002t0002g0046others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+1771T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898769 | ||||||
| chr6:157898830
|
C | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.472+1832C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157898830 | ||||||
| chr6:157899049
|
T | TAGGGGAG others(23): Show |
10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(7): Show | 10 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.472+2114_472+2143d others(32): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899049 | |||||
| chr6:157899049
|
T | TAGGGGAG others(83): Show |
1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.472+2054_472+2143d others(92): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899049 | |||||
| chr6:157899211
|
T | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.472+2213T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899211 | ||||||
| chr6:157899234
|
A | G | 1 | a0001c0011t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.472+2236A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899234 | ||||||
| chr6:157899275
|
C | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.472+2277C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899275 | ||||||
| chr6:157899646
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0243a0001c0001t0001g0249 | 3 | HG00621.hp2 NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.473-2252C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899646 | ||||||
| chr6:157899699
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.473-2199A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899699 | ||||||
| chr6:157899764
|
G | A | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.473-2134G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899764 | ||||||
| chr6:157899892
|
A | AGT | 55 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.473-1994_473-1993d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899892 | |||||
| chr6:157899892
|
A | AGTGTGT | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-1998_473-1993d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899892 | |||||
| chr6:157899892
|
A | AGTGTGTG others(1): Show |
21 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(18): Show | 21 | HG00099.hp2 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.473-2000_473-1993d others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899892 | |||||
| chr6:157899892
|
A | AGTGTGTG others(3): Show |
13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG00642.hp2 HG01891.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.473-2002_473-1993d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899892 | |||||
| chr6:157899892
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.473-2004_473-1993d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157899892 | |||||
| chr6:157899906
|
C | T | 96 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.473-1992C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899906 | ||||||
| chr6:157899907
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.473-1991G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899907 | ||||||
| chr6:157899927
|
G | A | 97 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(94): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.473-1971G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899927 | ||||||
| chr6:157899931
|
C | G | 95 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.473-1967C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157899931 | ||||||
| chr6:157900052
|
G | A | 9 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270others(6): Show | 9 | HG02602.hp1 HG02735.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-1846G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900052 | ||||||
| chr6:157900095
|
G | C | 101 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.473-1803G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900095 | ||||||
| chr6:157900378
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.473-1520A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900378 | ||||||
| chr6:157900440
|
A | G | 2 | a0001c0003t0003g0264a0001c0003t0003g0265 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.473-1458A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900440 | ||||||
| chr6:157900474
|
C | A | 101 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.473-1424C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900474 | ||||||
| chr6:157900475
|
C | G | 101 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.473-1423C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900475 | ||||||
| chr6:157900501
|
G | A | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.473-1397G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900501 | ||||||
| chr6:157900525
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.473-1373G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900525 | ||||||
| chr6:157900531
|
T | C | 102 | a0001c0001t0001g0297a0001c0001t0003g0250a0001c0001t0003g0257others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.473-1367T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900531 | ||||||
| chr6:157900532
|
G | C | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.473-1366G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900532 | ||||||
| chr6:157900853
|
C | T | 10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(7): Show | 10 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.473-1045C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900853 | ||||||
| chr6:157900866
|
C | T | 3 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296 | 3 | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.473-1032C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157900866 | ||||||
| chr6:157901268
|
G | T | 10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(7): Show | 10 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.473-630G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901268 | ||||||
| chr6:157901473
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.473-425G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901473 | ||||||
| chr6:157901569
|
T | TTGCATGT others(3): Show |
1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.473-328_473-327ins others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157901569 | |||||
| chr6:157901571
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.473-327C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901571 | ||||||
| chr6:157901608
|
C | T | 88 | a0001c0001t0013g0298a0001c0003t0003g0203a0001c0003t0003g0251others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.473-290C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901608 | ||||||
| chr6:157901620
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.473-278G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901620 | ||||||
| chr6:157901795
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.473-103T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | chr6 | 157901795 | ||||||
| chr6:157901854
|
CT | C | 88 | a0001c0001t0001g0244a0001c0001t0013g0298a0001c0003t0003g0203others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.473-30delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 157901854 | |||||
| chr6:157902212
|
T | TA | 10 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.620+179dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157902212 | |||||
| chr6:157902212
|
T | TAA | 13 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(10): Show | 13 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.620+178_620+179dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157902212 | |||||
| chr6:157902212
|
T | TAAA | 83 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.620+177_620+179dup others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157902212 | |||||
| chr6:157902238
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0228a0001c0001t0009g0132others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+193A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902238 | ||||||
| chr6:157902486
|
A | G | 2 | a0002c0002t0002g0031a0002c0002t0002g0033 | 2 | HG00597.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.620+441A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902486 | ||||||
| chr6:157902492
|
CCT | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+448_620+449del others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902492 | ||||||
| chr6:157902610
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+565G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902610 | ||||||
| chr6:157902659
|
A | G | 1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.620+614A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902659 | ||||||
| chr6:157902697
|
T | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(10): Show | 13 | HG02056.hp2 HG02523.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.620+652T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902697 | ||||||
| chr6:157902698
|
C | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(10): Show | 13 | HG02056.hp2 HG02523.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.620+653C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902698 | ||||||
| chr6:157902731
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+686G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902731 | ||||||
| chr6:157902761
|
G | A | 5 | a0001c0003t0003g0270a0001c0003t0003g0271a0001c0003t0003g0272others(2): Show | 5 | HG02602.hp1 HG02735.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.620+716G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157902761 | ||||||
| chr6:157903070
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.620+1025G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903070 | ||||||
| chr6:157903188
|
T | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+1143T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903188 | ||||||
| chr6:157903190
|
C | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+1145C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903190 | ||||||
| chr6:157903192
|
T | TCCAAAA | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+1147_620+1148i others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903192 | ||||||
| chr6:157903221
|
A | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.620+1176A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903221 | ||||||
| chr6:157903251
|
C | T | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.620+1206C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903251 | ||||||
| chr6:157903267
|
CAT | C | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.620+1224_620+1225d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157903267 | |||||
| chr6:157903279
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.620+1234C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903279 | ||||||
| chr6:157903304
|
G | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.620+1259G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903304 | ||||||
| chr6:157903373
|
A | G | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.620+1328A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903373 | ||||||
| chr6:157903509
|
A | T | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.620+1464A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903509 | ||||||
| chr6:157903598
|
T | C | 31 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(28): Show | 31 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.620+1553T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903598 | ||||||
| chr6:157903672
|
A | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(1): Show | 4 | HG02523.hp2 NA18947.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+1627A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903672 | ||||||
| chr6:157903713
|
T | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+1668T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903713 | ||||||
| chr6:157903764
|
TA | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.620+1721delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157903764 | |||||
| chr6:157903777
|
G | A | 1 | a0002c0002t0002g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.620+1732G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903777 | ||||||
| chr6:157903896
|
C | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.620+1851C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157903896 | ||||||
| chr6:157904097
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.621-2031T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904097 | ||||||
| chr6:157904412
|
C | T | 96 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.621-1716C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904412 | ||||||
| chr6:157904432
|
C | CA | 12 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.621-1686dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 157904432 | |||||
| chr6:157904602
|
T | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.621-1526T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904602 | ||||||
| chr6:157904699
|
A | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.621-1429A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904699 | ||||||
| chr6:157904866
|
G | A | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.621-1262G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904866 | ||||||
| chr6:157904896
|
A | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-1232A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157904896 | ||||||
| chr6:157905166
|
A | G | 1 | a0001c0011t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.621-962A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905166 | ||||||
| chr6:157905240
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.621-888C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905240 | ||||||
| chr6:157905302
|
C | A | 1 | a0002c0002t0002g0001 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.621-826C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905302 | ||||||
| chr6:157905309
|
A | T | 13 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0083others(10): Show | 13 | HG02056.hp2 HG02523.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.621-819A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905309 | ||||||
| chr6:157905384
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.621-744T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905384 | ||||||
| chr6:157905421
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.621-707C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905421 | ||||||
| chr6:157905672
|
G | T | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.621-456G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905672 | ||||||
| chr6:157905757
|
T | C | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-371T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157905757 | ||||||
| chr6:157906023
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01515.hp1 HG03831.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.621-105C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157906023 | ||||||
| chr6:157906033
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0244 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.621-95G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157906033 | ||||||
| chr6:157906095
|
T | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-33T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 6/17 | chr6 | 157906095 | ||||||
| chr6:157906237
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.705+25T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157906237 | ||||||
| chr6:157906263
|
T | C | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.705+51T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157906263 | ||||||
| chr6:157906490
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.705+278T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157906490 | ||||||
| chr6:157906582
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.705+370T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157906582 | ||||||
| chr6:157906596
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.705+384C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157906596 | ||||||
| chr6:157907087
|
A | T | 1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.705+875A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907087 | ||||||
| chr6:157907278
|
T | G | 1 | a0002c0002t0002g0017 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.705+1066T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907278 | ||||||
| chr6:157907278
|
T | TTTTG | 86 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.705+1082_705+1085d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 157907278 | |||||
| chr6:157907342
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 8 | HG00544.hp1 NA18612.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.705+1130T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907342 | ||||||
| chr6:157907457
|
G | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+1245G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907457 | ||||||
| chr6:157907474
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.705+1262C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907474 | ||||||
| chr6:157907527
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+1315G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907527 | ||||||
| chr6:157907527
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.705+1315G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907527 | ||||||
| chr6:157907575
|
C | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.705+1363C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907575 | ||||||
| chr6:157907663
|
C | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.705+1451C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907663 | ||||||
| chr6:157907795
|
TTG | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+1584_705+1585d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907795 | ||||||
| chr6:157907823
|
A | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.705+1611A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907823 | ||||||
| chr6:157907838
|
C | T | 3 | a0002c0002t0002g0003a0002c0002t0002g0007a0002c0002t0002g0008 | 3 | NA18960.hp1 NA19079.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.705+1626C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907838 | ||||||
| chr6:157907855
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.705+1643T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907855 | ||||||
| chr6:157907952
|
C | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1713C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157907952 | ||||||
| chr6:157908000
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.706-1665T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908000 | ||||||
| chr6:157908170
|
G | A | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.706-1495G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908170 | ||||||
| chr6:157908382
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0139 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.706-1283G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908382 | ||||||
| chr6:157908514
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.706-1151G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908514 | ||||||
| chr6:157908566
|
A | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.706-1099A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908566 | ||||||
| chr6:157908631
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.706-1034G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908631 | ||||||
| chr6:157908703
|
C | T | 1 | a0001c0003t0003g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.706-962C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908703 | ||||||
| chr6:157908746
|
T | TAC | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.706-916_706-915dup others(2): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 157908746 | |||||
| chr6:157908858
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.706-807T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908858 | ||||||
| chr6:157908886
|
G | A | 12 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-779G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908886 | ||||||
| chr6:157908937
|
G | C | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.706-728G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908937 | ||||||
| chr6:157908943
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.706-722G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908943 | ||||||
| chr6:157908971
|
G | A | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-694G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157908971 | ||||||
| chr6:157909097
|
C | G | 1 | a0001c0012t0001g0202 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.706-568C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157909097 | ||||||
| chr6:157909117
|
T | C | 103 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.706-548T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157909117 | ||||||
| chr6:157909446
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.706-219T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157909446 | ||||||
| chr6:157909449
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.706-216C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157909449 | ||||||
| chr6:157909652
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.706-13A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 7/17 | chr6 | 157909652 | ||||||
| chr6:157910118
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+93G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910118 | ||||||
| chr6:157910300
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.949+275T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910300 | ||||||
| chr6:157910649
|
C | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+624C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910649 | ||||||
| chr6:157910686
|
AGCACCTT others(13): Show |
A | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+682_949+701del others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157910686 | |||||
| chr6:157910732
|
A | G | 1 | a0001c0001t0004g0065 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.949+707A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910732 | ||||||
| chr6:157910855
|
A | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.949+830A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910855 | ||||||
| chr6:157910888
|
G | A | 18 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.949+863G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910888 | ||||||
| chr6:157910904
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.949+879G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910904 | ||||||
| chr6:157910917
|
C | T | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.949+892C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910917 | ||||||
| chr6:157910938
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0205 | 2 | HG00544.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.949+913G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910938 | ||||||
| chr6:157910984
|
G | A | 1 | a0001c0001t0003g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.949+959G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157910984 | ||||||
| chr6:157911037
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.949+1012C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911037 | ||||||
| chr6:157911112
|
C | CAAAT | 23 | a0001c0001t0001g0100a0001c0001t0001g0119a0001c0001t0001g0135others(20): Show | 23 | HG01934.hp1 HG01934.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.949+1116_949+1119d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157911112 | |||||
| chr6:157911112
|
C | CAAATAAA others(1): Show |
5 | a0001c0001t0004g0063a0001c0001t0004g0066a0001c0001t0004g0260others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+1112_949+1119d others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157911112 | |||||
| chr6:157911112
|
CAAATAAA others(1): Show |
C | 102 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.949+1112_949+1119d others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157911112 | |||||
| chr6:157911283
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.949+1258A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911283 | ||||||
| chr6:157911308
|
T | C | 12 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(9): Show | 12 | HG00544.hp2 HG03579.hp1 HG06807.hp1 others(9): Show |
intron_variant | MODIFIER | c.949+1283T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911308 | ||||||
| chr6:157911393
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.949+1368G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911393 | ||||||
| chr6:157911415
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0228a0001c0001t0009g0132others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.949+1390A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911415 | ||||||
| chr6:157911427
|
C | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+1402C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911427 | ||||||
| chr6:157911472
|
C | T | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.949+1447C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911472 | ||||||
| chr6:157911843
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.949+1818G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911843 | ||||||
| chr6:157911968
|
G | C | 14 | a0001c0001t0001g0151a0001c0001t0001g0157a0001c0001t0001g0206others(11): Show | 14 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.949+1943G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911968 | ||||||
| chr6:157911978
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+1953G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157911978 | ||||||
| chr6:157912037
|
C | T | 90 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.949+2012C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912037 | ||||||
| chr6:157912085
|
G | A | 102 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.949+2060G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912085 | ||||||
| chr6:157912154
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.949+2129A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912154 | ||||||
| chr6:157912420
|
T | TA | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+2404dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157912420 | |||||
| chr6:157912602
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.949+2577G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912602 | ||||||
| chr6:157912628
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.949+2603T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912628 | ||||||
| chr6:157912636
|
T | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+2611T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912636 | ||||||
| chr6:157912902
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.949+2877T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157912902 | ||||||
| chr6:157913093
|
C | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+3068C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913093 | ||||||
| chr6:157913226
|
AT | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+3203delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157913226 | |||||
| chr6:157913257
|
TA | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+3236delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157913257 | |||||
| chr6:157913290
|
A | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+3265A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913290 | ||||||
| chr6:157913301
|
T | TTTTA | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.949+3300_949+3303d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157913301 | |||||
| chr6:157913301
|
TTTTA | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+3300_949+3303d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157913301 | |||||
| chr6:157913425
|
C | CCTCAGCC others(6): Show |
91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.949+3400_949+3401i others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913425 | ||||||
| chr6:157913555
|
A | C | 1 | a0001c0001t0005g0289 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.949+3530A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913555 | ||||||
| chr6:157913568
|
T | C | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.949+3543T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913568 | ||||||
| chr6:157913664
|
C | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+3639C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913664 | ||||||
| chr6:157913765
|
G | A | 1 | a0001c0001t0003g0277 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.949+3740G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913765 | ||||||
| chr6:157913959
|
AT | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+3935delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157913959 | ||||||
| chr6:157914006
|
AAG | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0197others(2): Show | 5 | HG00735.hp2 HG01255.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.949+3984_949+3985d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914006 | |||||
| chr6:157914110
|
A | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+4085A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914110 | ||||||
| chr6:157914180
|
A | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.949+4155A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914180 | ||||||
| chr6:157914304
|
T | G | 102 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.949+4279T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914304 | ||||||
| chr6:157914463
|
C | CT | 34 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0266others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.949+4443dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914463 | |||||
| chr6:157914463
|
C | CTT | 10 | a0001c0003t0003g0251a0001c0003t0003g0252a0001c0003t0003g0253others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.949+4442_949+4443d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914463 | |||||
| chr6:157914469
|
C | CT | 104 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0084others(101): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.949+4467dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTT | 12 | a0001c0001t0001g0069a0001c0001t0001g0131a0001c0001t0001g0159others(9): Show | 12 | HG01071.hp1 HG02622.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.949+4466_949+4467d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTTT | 6 | a0001c0001t0001g0225a0001c0001t0004g0063a0001c0001t0004g0065others(3): Show | 6 | HG01891.hp2 HG03195.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+4465_949+4467d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.949+4456_949+4467d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.949+4449_949+4467d others(21): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.949+4448_949+4467d others(22): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.949+4467_949+4468i others(34): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914469 | |||||
| chr6:157914469
|
C | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+4444C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914469 | ||||||
| chr6:157914480
|
T | TTTTTTTT others(1): Show |
11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+4462_949+4463i others(10): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157914480 | |||||
| chr6:157914500
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0227 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.949+4475G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914500 | ||||||
| chr6:157914970
|
T | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+4945T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157914970 | ||||||
| chr6:157915007
|
A | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.949+4982A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915007 | ||||||
| chr6:157915053
|
C | A | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.949+5028C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915053 | ||||||
| chr6:157915170
|
T | C | 102 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.949+5145T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915170 | ||||||
| chr6:157915231
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.949+5206A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915231 | ||||||
| chr6:157915351
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.949+5326C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915351 | ||||||
| chr6:157915352
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.949+5327G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915352 | ||||||
| chr6:157915421
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.949+5396G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915421 | ||||||
| chr6:157915623
|
T | TA | 8 | a0001c0001t0001g0156a0001c0001t0001g0165a0001c0001t0001g0174others(5): Show | 8 | HG02015.hp1 HG02135.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.949+5616dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915623 | |||||
| chr6:157915623
|
T | TAAAA | 9 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0003g0296others(6): Show | 9 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+5613_949+5616d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915623 | |||||
| chr6:157915623
|
T | TAAAAAAA others(5): Show |
3 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0019g0062 | 3 | HG03195.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.949+5605_949+5616d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915623 | |||||
| chr6:157915623
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0004g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.949+5604_949+5616d others(15): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915623 | |||||
| chr6:157915623
|
TA | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143others(9): Show | 12 | HG00733.hp1 HG01496.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.949+5616delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915623 | |||||
| chr6:157915636
|
A | AATATATA others(7): Show |
1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.949+5612_949+5613i others(16): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915636 | |||||
| chr6:157915636
|
A | AATATATA others(15): Show |
1 | a0002c0002t0002g0039 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.949+5612_949+5613i others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915636 | |||||
| chr6:157915638
|
A | AATATATA others(3): Show |
1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.949+5614_949+5615i others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915638 | |||||
| chr6:157915638
|
A | T | 2 | a0001c0001t0018g0302a0002c0002t0002g0039 | 2 | HG06807.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.949+5613A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915638 | ||||||
| chr6:157915640
|
A | AAAAAAAA others(57): Show |
1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(66): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(28): Show |
1 | a0002c0002t0002g0001 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(27): Show |
1 | a0002c0002t0002g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(33): Show |
1 | a0002c0002t0002g0004 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(42): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(41): Show |
1 | a0002c0002t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(50): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(24): Show |
2 | a0002c0002t0002g0036a0002c0002t0002g0038 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(33): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(26): Show |
2 | a0002c0002t0002g0025a0002c0002t0002g0026 | 2 | HG01346.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(35): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(28): Show |
6 | a0002c0002t0002g0011a0002c0002t0002g0012a0002c0002t0002g0019others(3): Show | 6 | HG00408.hp2 HG00642.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+5616_949+5617i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(30): Show |
1 | a0002c0002t0002g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(39): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(41): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(40): Show |
1 | a0002c0002t0002g0041 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(49): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(27): Show |
9 | a0002c0002t0002g0013a0002c0002t0002g0015a0002c0002t0002g0021others(6): Show | 9 | HG00280.hp1 HG00621.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.949+5616_949+5617i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(29): Show |
1 | a0002c0002t0002g0007 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(38): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(40): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(33): Show |
1 | a0002c0002t0002g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(42): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(10): Show |
1 | a0002c0002t0002g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(19): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(26): Show |
3 | a0002c0002t0002g0016a0002c0002t0008g0022a0002c0002t0008g0024 | 3 | HG00733.hp2 HG00735.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(35): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(28): Show |
5 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0010others(2): Show | 5 | HG03654.hp1 HG03688.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+5616_949+5617i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(30): Show |
2 | a0002c0002t0002g0003a0002c0002t0002g0023 | 2 | HG03942.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(39): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(32): Show |
2 | a0002c0002t0002g0002a0002c0002t0002g0051 | 2 | NA18975.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(41): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0004g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(13): Show |
1 | a0002c0002t0002g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(22): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(27): Show |
3 | a0002c0002t0002g0014a0002c0002t0002g0017a0002c0002t0002g0042 | 3 | HG00438.hp2 HG02129.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(36): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(44): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(16): Show |
1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(25): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(24): Show |
1 | a0002c0002t0002g0030 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(33): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(28): Show |
2 | a0001c0003t0003g0258a0002c0002t0002g0055 | 2 | HG02083.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(37): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(30): Show |
1 | a0002c0002t0002g0040 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(39): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(41): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0004g0260 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(46): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(47): Show |
1 | a0001c0003t0003g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(56): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(51): Show |
1 | a0002c0002t0012g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(60): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(26): Show |
1 | a0002c0002t0002g0037 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(35): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(40): Show |
1 | a0001c0003t0003g0271 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(49): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(42): Show |
1 | a0001c0003t0003g0276 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(51): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(44): Show |
1 | a0001c0003t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(48): Show |
1 | a0001c0003t0003g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(57): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(39): Show |
1 | a0001c0003t0003g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(38): Show |
1 | a0001c0003t0003g0270 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(47): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(40): Show |
1 | a0001c0003t0003g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(49): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(42): Show |
1 | a0001c0003t0003g0275 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(51): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(44): Show |
1 | a0001c0003t0003g0273 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAA others(48): Show |
1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(57): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAAAT others(40): Show |
1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.949+5616_949+5617i others(49): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAATA others(15): Show |
1 | a0001c0003t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(24): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAAAATA others(39): Show |
1 | a0001c0003t0003g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(48): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAATATA others(9): Show |
8 | a0001c0003t0003g0203a0001c0003t0003g0252a0001c0003t0003g0254others(5): Show | 8 | HG01081.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.949+5616_949+5617i others(18): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAATATA others(11): Show |
4 | a0001c0003t0003g0251a0001c0003t0003g0253a0001c0003t0003g0279others(1): Show | 4 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+5616_949+5617i others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAAATATA others(17): Show |
3 | a0001c0003t0003g0285a0004c0005t0003g0282a0004c0005t0003g0283 | 3 | HG00642.hp2 HG01175.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.949+5616_949+5617i others(26): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AAATATAT others(8): Show |
1 | a0001c0003t0003g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.949+5616_949+5617i others(17): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915640 | |||||
| chr6:157915640
|
A | AT | 3 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0016g0076 | 3 | HG00544.hp1 HG00558.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.949+5615_949+5616i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915640 | ||||||
| chr6:157915640
|
A | T | 18 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(15): Show | 18 | HG01257.hp2 HG02083.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.949+5615A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915640 | ||||||
| chr6:157915641
|
AT | A | 61 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0085others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.949+5617delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915641 | ||||||
| chr6:157915642
|
T | A | 38 | a0001c0001t0001g0069a0001c0001t0001g0103a0001c0001t0001g0153others(35): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.949+5617T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915642 | ||||||
| chr6:157915644
|
T | A | 31 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(28): Show | 31 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.949+5619T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915644 | ||||||
| chr6:157915644
|
T | C | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.949+5619T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915644 | ||||||
| chr6:157915646
|
T | C | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.949+5621T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915646 | ||||||
| chr6:157915654
|
T | C | 1 | a0001c0001t0020g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.949+5629T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915654 | ||||||
| chr6:157915657
|
A | G | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.949+5632A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915657 | ||||||
| chr6:157915658
|
C | T | 89 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.949+5633C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915658 | ||||||
| chr6:157915660
|
C | T | 12 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.949+5635C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915660 | ||||||
| chr6:157915668
|
C | A | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.949+5643C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915668 | ||||||
| chr6:157915670
|
C | A | 55 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.949+5645C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915670 | ||||||
| chr6:157915767
|
G | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.949+5742G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915767 | ||||||
| chr6:157915803
|
C | T | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-5728C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915803 | ||||||
| chr6:157915804
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.950-5727G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915804 | ||||||
| chr6:157915822
|
C | CAAAAAAA others(8): Show |
10 | a0001c0001t0018g0302a0001c0003t0003g0266a0001c0003t0003g0269others(7): Show | 10 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.950-5695_950-5694i others(17): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915822 | |||||
| chr6:157915822
|
C | CAAAAAAA others(9): Show |
39 | a0001c0003t0003g0251a0001c0003t0003g0253a0001c0003t0003g0258others(36): Show | 39 | HG00280.hp1 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.950-5695_950-5694i others(18): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915822 | |||||
| chr6:157915822
|
C | CAAAAAAA others(10): Show |
37 | a0001c0001t0011g0060a0001c0003t0003g0203a0001c0003t0003g0252others(34): Show | 37 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.950-5695_950-5694i others(19): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915822 | |||||
| chr6:157915822
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0011g0259a0001c0003t0003g0281a0002c0002t0002g0012others(1): Show | 4 | HG01106.hp2 HG02056.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.950-5695_950-5694i others(20): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915822 | |||||
| chr6:157915822
|
CA | C | 20 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(17): Show | 20 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.950-5695delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157915822 | |||||
| chr6:157915885
|
G | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-5646G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915885 | ||||||
| chr6:157915922
|
A | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-5609A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915922 | ||||||
| chr6:157915989
|
C | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-5542C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157915989 | ||||||
| chr6:157916023
|
T | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-5508T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916023 | ||||||
| chr6:157916045
|
T | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.950-5486T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916045 | ||||||
| chr6:157916057
|
C | T | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.950-5474C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916057 | ||||||
| chr6:157916092
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-5439T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916092 | ||||||
| chr6:157916144
|
C | T | 1 | a0002c0007t0007g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.950-5387C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916144 | ||||||
| chr6:157916170
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.950-5361G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916170 | ||||||
| chr6:157916318
|
G | A | 107 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0088others(104): Show | 107 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.950-5213G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916318 | ||||||
| chr6:157916329
|
C | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-5202C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916329 | ||||||
| chr6:157916330
|
G | A | 10 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(7): Show | 10 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.950-5201G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916330 | ||||||
| chr6:157916401
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.950-5130A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916401 | ||||||
| chr6:157916417
|
C | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-5114C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916417 | ||||||
| chr6:157916439
|
C | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-5092C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916439 | ||||||
| chr6:157916460
|
C | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-5071C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916460 | ||||||
| chr6:157916706
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.950-4825A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916706 | ||||||
| chr6:157916780
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.950-4751G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157916780 | ||||||
| chr6:157916968
|
TTA | T | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-4558_950-4557d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157916968 | |||||
| chr6:157917134
|
C | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.950-4397C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917134 | ||||||
| chr6:157917433
|
T | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-4098T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917433 | ||||||
| chr6:157917498
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.950-4033A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917498 | ||||||
| chr6:157917608
|
A | G | 4 | a0001c0003t0003g0285a0001c0003t0003g0286a0004c0005t0003g0282others(1): Show | 4 | HG00099.hp2 HG00642.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.950-3923A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917608 | ||||||
| chr6:157917624
|
T | G | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.950-3907T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917624 | ||||||
| chr6:157917686
|
C | T | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.950-3845C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917686 | ||||||
| chr6:157917740
|
C | T | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-3791C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917740 | ||||||
| chr6:157917965
|
T | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.950-3566T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157917965 | ||||||
| chr6:157918176
|
C | T | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.950-3355C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157918176 | ||||||
| chr6:157918459
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-3072T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157918459 | ||||||
| chr6:157918484
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-3047G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157918484 | ||||||
| chr6:157918935
|
A | G | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.950-2596A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157918935 | ||||||
| chr6:157919168
|
A | G | 1 | a0006c0014t0001g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.950-2363A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919168 | ||||||
| chr6:157919177
|
G | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-2354G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919177 | ||||||
| chr6:157919464
|
TCTG | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-2064_950-2062d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157919464 | |||||
| chr6:157919785
|
G | A | 28 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.950-1746G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919785 | ||||||
| chr6:157919813
|
G | A | 2 | a0002c0002t0002g0051a0002c0002t0002g0052 | 2 | NA19011.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.950-1718G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919813 | ||||||
| chr6:157919817
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-1714T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919817 | ||||||
| chr6:157919871
|
T | G | 1 | a0002c0002t0002g0056 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.950-1660T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157919871 | ||||||
| chr6:157919904
|
G | GC | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.950-1625dupC | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157919904 | |||||
| chr6:157919953
|
C | CTGTT | 75 | a0001c0001t0001g0188a0001c0001t0001g0234a0001c0001t0001g0235others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.950-1552_950-1549d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157919953 | |||||
| chr6:157919953
|
C | CTGTTTGT others(5): Show |
1 | a0002c0002t0002g0016 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.950-1560_950-1549d others(14): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 157919953 | |||||
| chr6:157920018
|
T | C | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-1513T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920018 | ||||||
| chr6:157920094
|
T | C | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-1437T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920094 | ||||||
| chr6:157920475
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.950-1056C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920475 | ||||||
| chr6:157920490
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.950-1041C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920490 | ||||||
| chr6:157920591
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-940G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920591 | ||||||
| chr6:157920606
|
A | G | 9 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | HG00544.hp1 NA18612.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.950-925A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920606 | ||||||
| chr6:157920727
|
G | A | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.950-804G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920727 | ||||||
| chr6:157920924
|
G | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0057 | 2 | NA18987.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.950-607G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157920924 | ||||||
| chr6:157921254
|
C | T | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.950-277C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157921254 | ||||||
| chr6:157921340
|
C | T | 6 | a0001c0001t0005g0288a0001c0001t0005g0289a0001c0001t0005g0293others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.950-191C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157921340 | ||||||
| chr6:157921426
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.950-105C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | chr6 | 157921426 | ||||||
| chr6:157921766
|
C | G | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1080+105C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157921766 | ||||||
| chr6:157921990
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0001t0001g0152 | 3 | HG00280.hp2 HG01106.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1080+329G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157921990 | ||||||
| chr6:157922207
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1080+546A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922207 | ||||||
| chr6:157922289
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0244 | 2 | HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1080+628T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922289 | ||||||
| chr6:157922362
|
C | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1080+701C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922362 | ||||||
| chr6:157922755
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1080+1094A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922755 | ||||||
| chr6:157922774
|
C | T | 18 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1080+1113C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922774 | ||||||
| chr6:157922792
|
A | G | 1 | a0002c0002t0002g0002 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1080+1131A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922792 | ||||||
| chr6:157922864
|
C | A | 1 | a0001c0001t0014g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1080+1203C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157922864 | ||||||
| chr6:157923104
|
G | A | 1 | a0001c0003t0003g0286 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1080+1443G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923104 | ||||||
| chr6:157923151
|
G | A | 1 | a0004c0005t0003g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1080+1490G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923151 | ||||||
| chr6:157923278
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1080+1617A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923278 | ||||||
| chr6:157923428
|
T | TA | 24 | a0001c0001t0001g0119a0001c0001t0001g0138a0001c0001t0001g0247others(21): Show | 24 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1080+1777dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157923428 | |||||
| chr6:157923428
|
T | TAA | 84 | a0001c0001t0013g0298a0001c0003t0003g0251a0001c0003t0003g0252others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1080+1776_1080+177 others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157923428 | |||||
| chr6:157923439
|
T | A | 113 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1080+1778T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923439 | ||||||
| chr6:157923586
|
T | C | 1 | a0002c0002t0002g0021 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1080+1925T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923586 | ||||||
| chr6:157923805
|
G | A | 92 | a0001c0001t0001g0165a0001c0001t0011g0060a0001c0001t0011g0259others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1080+2144G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923805 | ||||||
| chr6:157923860
|
A | G | 1 | a0001c0001t0010g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1080+2199A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923860 | ||||||
| chr6:157923959
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1080+2298A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923959 | ||||||
| chr6:157923971
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1080+2310G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923971 | ||||||
| chr6:157923973
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1080+2312G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923973 | ||||||
| chr6:157923983
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1080+2322A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157923983 | ||||||
| chr6:157924014
|
A | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1080+2353A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924014 | ||||||
| chr6:157924050
|
T | G | 110 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0001g0084others(107): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1080+2389T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924050 | ||||||
| chr6:157924160
|
G | T | 1 | a0001c0001t0019g0062 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1080+2499G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924160 | ||||||
| chr6:157924164
|
T | A | 1 | a0001c0001t0001g0238 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1080+2503T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924164 | ||||||
| chr6:157924293
|
A | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+2632A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924293 | ||||||
| chr6:157924753
|
G | A | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-2358G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924753 | ||||||
| chr6:157924753
|
G | T | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1081-2358G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924753 | ||||||
| chr6:157924855
|
G | A | 31 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(28): Show | 31 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1081-2256G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157924855 | ||||||
| chr6:157925124
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-1987A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925124 | ||||||
| chr6:157925231
|
A | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1081-1880A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925231 | ||||||
| chr6:157925242
|
TGTAGAAA others(718): Show |
T | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1081-1866_1081-114 others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157925242 | |||||
| chr6:157925254
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1081-1857C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925254 | ||||||
| chr6:157925292
|
C | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-1819C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925292 | ||||||
| chr6:157925301
|
A | C | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1081-1810A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925301 | ||||||
| chr6:157925438
|
A | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1081-1673A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925438 | ||||||
| chr6:157925599
|
C | T | 3 | a0001c0001t0011g0259a0001c0001t0013g0298a0001c0001t0018g0302 | 3 | HG02559.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-1512C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925599 | ||||||
| chr6:157925625
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1081-1486G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925625 | ||||||
| chr6:157925903
|
A | G | 53 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(50): Show | 53 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1081-1208A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157925903 | ||||||
| chr6:157926388
|
A | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-723A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157926388 | ||||||
| chr6:157926547
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1081-564T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157926547 | ||||||
| chr6:157926585
|
C | G | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1081-526C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157926585 | ||||||
| chr6:157926780
|
C | CA | 17 | a0001c0001t0001g0073a0001c0001t0001g0116a0001c0001t0001g0118others(14): Show | 17 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1081-307dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157926780 | |||||
| chr6:157926780
|
CA | C | 36 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0138others(33): Show | 36 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1081-307delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157926780 | |||||
| chr6:157926780
|
CAA | C | 59 | a0001c0001t0001g0189a0001c0003t0003g0263a0001c0003t0003g0264others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1081-308_1081-307d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 157926780 | |||||
| chr6:157926868
|
T | C | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1081-243T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 10/17 | chr6 | 157926868 | ||||||
| chr6:157927293
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1184+79C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927293 | ||||||
| chr6:157927296
|
A | G | 2 | a0002c0002t0002g0035a0002c0002t0002g0053 | 2 | NA19001.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1184+82A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927296 | ||||||
| chr6:157927447
|
T | C | 2 | a0003c0006t0001g0120a0003c0006t0001g0141 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1184+233T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927447 | ||||||
| chr6:157927455
|
A | G | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+241A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927455 | ||||||
| chr6:157927478
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1184+264A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927478 | ||||||
| chr6:157927497
|
C | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1184+283C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927497 | ||||||
| chr6:157927718
|
C | CT | 34 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0091others(31): Show | 34 | HG00423.hp2 HG00735.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.1184+530dupT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927718 | |||||
| chr6:157927718
|
C | CTT | 11 | a0001c0001t0001g0210a0001c0001t0003g0277a0001c0001t0003g0278others(8): Show | 11 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+529_1184+530d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927718 | |||||
| chr6:157927718
|
CT | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0143others(3): Show | 6 | HG02083.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+530delT | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927718 | |||||
| chr6:157927718
|
CTTTTTTT others(2): Show |
C | 84 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+522_1184+530d others(11): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927718 | |||||
| chr6:157927749
|
C | T | 1 | a0001c0001t0010g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1184+535C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927749 | ||||||
| chr6:157927772
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1184+558G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927772 | ||||||
| chr6:157927781
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1184+567C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927781 | ||||||
| chr6:157927864
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1184+650C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927864 | ||||||
| chr6:157927882
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1184+668T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157927882 | ||||||
| chr6:157927930
|
A | AAC | 77 | a0001c0001t0001g0129a0001c0001t0001g0167a0001c0001t0001g0222others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1185-647_1185-646d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927930 | |||||
| chr6:157927930
|
A | AACAC | 6 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(3): Show | 6 | HG00642.hp2 HG01106.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-649_1185-646d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927930 | |||||
| chr6:157927930
|
A | AACACAC | 9 | a0001c0003t0003g0268a0001c0003t0003g0269a0001c0003t0003g0270others(6): Show | 9 | HG02602.hp1 HG02735.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185-651_1185-646d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927930 | |||||
| chr6:157927930
|
AACACAC | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1185-651_1185-646d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 157927930 | |||||
| chr6:157928218
|
C | T | 102 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1185-381C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 11/17 | chr6 | 157928218 | ||||||
| chr6:157928738
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1288+36G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157928738 | ||||||
| chr6:157928757
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1288+55T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157928757 | ||||||
| chr6:157928861
|
T | C | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1288+159T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157928861 | ||||||
| chr6:157929004
|
G | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1288+302G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929004 | ||||||
| chr6:157929065
|
G | A | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+363G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929065 | ||||||
| chr6:157929219
|
T | C | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+517T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929219 | ||||||
| chr6:157929280
|
C | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1288+578C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929280 | ||||||
| chr6:157929323
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1288+621C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929323 | ||||||
| chr6:157929396
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1288+694A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929396 | ||||||
| chr6:157929427
|
C | T | 1 | a0001c0003t0003g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1288+725C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929427 | ||||||
| chr6:157929461
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1288+759T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929461 | ||||||
| chr6:157929689
|
G | A | 11 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG01934.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1288+987G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929689 | ||||||
| chr6:157929783
|
G | GC | 111 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1288+1081_1288+108 others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929783 | ||||||
| chr6:157929999
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0126 | 2 | HG02698.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1288+1297G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157929999 | ||||||
| chr6:157930246
|
G | A | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+1544G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930246 | ||||||
| chr6:157930282
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1288+1580T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930282 | ||||||
| chr6:157930395
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1288+1693A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930395 | ||||||
| chr6:157930469
|
G | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0057 | 2 | NA18987.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1289-1726G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930469 | ||||||
| chr6:157930538
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1289-1657T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930538 | ||||||
| chr6:157930561
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1289-1634G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930561 | ||||||
| chr6:157930624
|
A | G | 1 | a0001c0003t0003g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1289-1571A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930624 | ||||||
| chr6:157930665
|
T | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1289-1530T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930665 | ||||||
| chr6:157930733
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1289-1462T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930733 | ||||||
| chr6:157930791
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1289-1404T>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157930791 | ||||||
| chr6:157931082
|
T | C | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-1113T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931082 | ||||||
| chr6:157931198
|
G | GTGTAGAA others(4): Show |
1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1289-997_1289-996i others(13): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931198 | ||||||
| chr6:157931244
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1289-951C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931244 | ||||||
| chr6:157931244
|
C | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1289-951C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931244 | ||||||
| chr6:157931252
|
G | C | 1 | a0001c0010t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1289-943G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931252 | ||||||
| chr6:157931286
|
T | TG | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-909_1289-908i others(3): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931286 | ||||||
| chr6:157931399
|
A | C | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1289-796A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931399 | ||||||
| chr6:157931443
|
C | T | 2 | a0001c0001t0003g0250a0001c0001t0003g0257 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1289-752C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931443 | ||||||
| chr6:157931547
|
TAA | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099 | 3 | HG00558.hp1 HG02135.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1289-644_1289-643d others(4): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 157931547 | |||||
| chr6:157931552
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099 | 3 | HG00558.hp1 HG02135.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1289-643A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931552 | ||||||
| chr6:157931556
|
ACCTTAG | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0099 | 3 | HG00558.hp1 HG02135.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1289-638_1289-633d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931556 | ||||||
| chr6:157931777
|
A | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-418A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931777 | ||||||
| chr6:157931856
|
G | C | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1289-339G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931856 | ||||||
| chr6:157931888
|
G | A | 1 | a0001c0003t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1289-307G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157931888 | ||||||
| chr6:157932171
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1289-24C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 12/17 | chr6 | 157932171 | ||||||
| chr6:157932639
|
G | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1366+367G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932639 | ||||||
| chr6:157932694
|
C | A | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1366+422C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932694 | ||||||
| chr6:157932694
|
C | G | 86 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(83): Show | 86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1366+422C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932694 | ||||||
| chr6:157932762
|
G | A | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1366+490G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932762 | ||||||
| chr6:157932791
|
C | T | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1366+519C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932791 | ||||||
| chr6:157932866
|
C | CA | 44 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0115others(41): Show | 44 | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1366+622dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157932866 | |||||
| chr6:157932866
|
CAAAAA | C | 20 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(17): Show | 20 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1366+618_1366+622d others(7): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157932866 | |||||
| chr6:157932866
|
CAAAAAA | C | 62 | a0001c0003t0003g0258a0001c0003t0003g0263a0001c0003t0003g0264others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1366+617_1366+622d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157932866 | |||||
| chr6:157932885
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1366+614_1366+623d others(12): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157932885 | ||||||
| chr6:157933011
|
A | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1366+739A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933011 | ||||||
| chr6:157933026
|
T | C | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1366+754T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933026 | ||||||
| chr6:157933096
|
A | G | 113 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1366+824A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933096 | ||||||
| chr6:157933101
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1366+829A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933101 | ||||||
| chr6:157933226
|
C | T | 2 | a0002c0002t0002g0016a0002c0002t0002g0017 | 2 | HG02129.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1366+954C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933226 | ||||||
| chr6:157933264
|
A | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1366+992A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933264 | ||||||
| chr6:157933299
|
AAAAAG | A | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1366+1030_1366+103 others(9): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157933299 | |||||
| chr6:157933300
|
A | C | 1 | a0001c0003t0003g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1366+1028A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933300 | ||||||
| chr6:157933364
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1366+1092T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933364 | ||||||
| chr6:157933545
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0109others(1): Show | 4 | HG02523.hp2 NA18947.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+1273A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933545 | ||||||
| chr6:157933783
|
G | A | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+1511G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933783 | ||||||
| chr6:157933825
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1366+1553G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933825 | ||||||
| chr6:157933863
|
C | T | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1366+1591C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933863 | ||||||
| chr6:157933997
|
T | C | 1 | a0002c0002t0002g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1366+1725T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157933997 | ||||||
| chr6:157934122
|
G | A | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1367-1842G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157934122 | ||||||
| chr6:157934313
|
GGA | G | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1367-1640_1367-163 others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157934313 | |||||
| chr6:157934462
|
A | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1367-1502A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157934462 | ||||||
| chr6:157934866
|
C | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1367-1098C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157934866 | ||||||
| chr6:157934985
|
A | G | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-979A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157934985 | ||||||
| chr6:157934998
|
ATAAT | A | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-961_1367-958d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 157934998 | |||||
| chr6:157935225
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1367-739T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935225 | ||||||
| chr6:157935311
|
T | C | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367-653T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935311 | ||||||
| chr6:157935315
|
G | A | 1 | a0001c0003t0003g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1367-649G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935315 | ||||||
| chr6:157935367
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1367-597G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935367 | ||||||
| chr6:157935400
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367-564C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935400 | ||||||
| chr6:157935425
|
G | A | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-539G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935425 | ||||||
| chr6:157935428
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1367-536G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935428 | ||||||
| chr6:157935491
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(3): Show | 6 | HG02145.hp2 HG02895.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367-473C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935491 | ||||||
| chr6:157935511
|
G | A | 1 | a0002c0002t0002g0033 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1367-453G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935511 | ||||||
| chr6:157935571
|
G | A | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1367-393G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935571 | ||||||
| chr6:157935664
|
A | G | 92 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1367-300A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935664 | ||||||
| chr6:157935702
|
C | T | 1 | a0001c0009t0006g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1367-262C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935702 | ||||||
| chr6:157935757
|
C | T | 7 | a0001c0001t0001g0188a0001c0001t0001g0191a0001c0001t0001g0194others(4): Show | 7 | HG00735.hp2 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367-207C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935757 | ||||||
| chr6:157935853
|
G | A | 1 | a0001c0001t0018g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1367-111G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935853 | ||||||
| chr6:157935903
|
T | G | 9 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367-61T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 13/17 | chr6 | 157935903 | ||||||
| chr6:157936048
|
C | T | 4 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(1): Show | 4 | HG02559.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1443+8C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936048 | ||||||
| chr6:157936057
|
A | G | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1443+17A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936057 | ||||||
| chr6:157936169
|
T | G | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1443+129T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936169 | ||||||
| chr6:157936355
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1443+315A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936355 | ||||||
| chr6:157936431
|
C | T | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1443+391C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936431 | ||||||
| chr6:157936510
|
G | A | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1443+470G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936510 | ||||||
| chr6:157936553
|
C | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1443+513C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936553 | ||||||
| chr6:157936592
|
C | T | 1 | a0001c0003t0003g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1443+552C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936592 | ||||||
| chr6:157936829
|
A | T | 39 | a0001c0001t0001g0069a0001c0001t0001g0088a0001c0001t0001g0121others(36): Show | 39 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1444-605A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936829 | ||||||
| chr6:157936853
|
C | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1444-581C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936853 | ||||||
| chr6:157936936
|
C | T | 1 | a0002c0007t0007g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1444-498C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936936 | ||||||
| chr6:157936980
|
AAAG | A | 18 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1444-453_1444-451d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157936980 | ||||||
| chr6:157937006
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0245 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1444-428A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157937006 | ||||||
| chr6:157937063
|
A | AGTT | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1444-370_1444-368d others(5): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr6 | 157937063 | |||||
| chr6:157937222
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1444-212A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157937222 | ||||||
| chr6:157937339
|
C | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1444-95C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 14/17 | chr6 | 157937339 | ||||||
| chr6:157937590
|
A | G | 2 | a0002c0002t0002g0027a0002c0002t0002g0029 | 2 | HG00642.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1533+67A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937590 | ||||||
| chr6:157937622
|
GAAAC | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1533+102_1533+105d others(6): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr6 | 157937622 | |||||
| chr6:157937735
|
C | A | 2 | a0001c0001t0001g0103a0001c0013t0001g0105 | 2 | HG00438.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1533+212C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937735 | ||||||
| chr6:157937741
|
A | G | 1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1533+218A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937741 | ||||||
| chr6:157937914
|
G | A | 2 | a0002c0002t0002g0036a0002c0002t0002g0038 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1533+391G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937914 | ||||||
| chr6:157937950
|
A | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1533+427A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937950 | ||||||
| chr6:157937951
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1533+428A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937951 | ||||||
| chr6:157937971
|
A | C | 124 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0136others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1533+448A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157937971 | ||||||
| chr6:157938032
|
T | C | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1533+509T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157938032 | ||||||
| chr6:157938236
|
T | C | 5 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(2): Show | 5 | HG03195.hp2 HG03225.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534-397T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157938236 | ||||||
| chr6:157938443
|
A | G | 87 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(84): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1534-190A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 15/17 | chr6 | 157938443 | ||||||
| chr6:157938781
|
GA | G | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1648+36delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 157938781 | |||||
| chr6:157938785
|
T | G | 91 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0013g0298others(88): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1648+38T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157938785 | ||||||
| chr6:157938850
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1648+103A>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157938850 | ||||||
| chr6:157938884
|
C | T | 11 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1648+137C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157938884 | ||||||
| chr6:157938885
|
C | G | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1648+138C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157938885 | ||||||
| chr6:157939144
|
G | GA | 56 | a0001c0009t0006g0058a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1648+407dupA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 157939144 | |||||
| chr6:157939152
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0259a0001c0001t0018g0302 | 3 | HG03579.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1648+405A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939152 | ||||||
| chr6:157939242
|
G | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1648+495G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939242 | ||||||
| chr6:157939366
|
T | C | 2 | a0001c0003t0003g0279a0001c0003t0003g0281 | 2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1648+619T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939366 | ||||||
| chr6:157939394
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1648+647G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939394 | ||||||
| chr6:157939426
|
TA | T | 113 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0003g0250others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1648+688delA | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 157939426 | |||||
| chr6:157939463
|
G | A | 68 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(65): Show | 68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1648+716G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939463 | ||||||
| chr6:157939472
|
G | A | 17 | a0001c0003t0003g0203a0001c0003t0003g0251a0001c0003t0003g0252others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1648+725G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939472 | ||||||
| chr6:157939553
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1648+806T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939553 | ||||||
| chr6:157939659
|
G | A | 28 | a0001c0001t0011g0060a0001c0003t0003g0203a0001c0003t0003g0251others(25): Show | 28 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1648+912G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939659 | ||||||
| chr6:157939873
|
C | G | 17 | a0001c0001t0001g0147a0001c0001t0013g0298a0001c0003t0003g0263others(14): Show | 17 | HG01891.hp1 HG02559.hp2 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1649-1010C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939873 | ||||||
| chr6:157939957
|
G | GGGGGCA | 52 | a0001c0001t0001g0084a0001c0001t0001g0159a0001c0001t0001g0160others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1649-915_1649-910d others(8): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr6 | 157939957 | |||||
| chr6:157939967
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1649-916G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157939967 | ||||||
| chr6:157940010
|
A | T | 25 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0146others(22): Show | 25 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1649-873A>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940010 | ||||||
| chr6:157940033
|
T | G | 116 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0070others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1649-850T>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940033 | ||||||
| chr6:157940097
|
G | A | 21 | a0001c0001t0003g0250a0001c0001t0003g0257a0001c0001t0003g0277others(18): Show | 21 | HG00099.hp2 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1649-786G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940097 | ||||||
| chr6:157940124
|
C | T | 1 | a0001c0003t0022g0292 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1649-759C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940124 | ||||||
| chr6:157940295
|
G | A | 7 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(4): Show | 7 | HG02055.hp1 HG02970.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1649-588G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940295 | ||||||
| chr6:157940398
|
A | G | 1 | a0001c0001t0011g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1649-485A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940398 | ||||||
| chr6:157940742
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1649-141A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940742 | ||||||
| chr6:157940791
|
G | C | 56 | a0001c0001t0006g0097a0002c0002t0002g0001a0002c0002t0002g0002others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1649-92G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940791 | ||||||
| chr6:157940863
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1649-20T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940863 | ||||||
| chr6:157940867
|
C | T | 276 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1649-16C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 16/17 | chr6 | 157940867 | ||||||
| chr6:157941102
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1740+128T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941102 | ||||||
| chr6:157941199
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1740+225G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941199 | ||||||
| chr6:157941228
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1740+254C>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941228 | ||||||
| chr6:157941252
|
G | A | 10 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1740+278G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941252 | ||||||
| chr6:157941482
|
G | A | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1740+508G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941482 | ||||||
| chr6:157941492
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1740+518A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941492 | ||||||
| chr6:157941565
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1740+591T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941565 | ||||||
| chr6:157941651
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1740+677A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941651 | ||||||
| chr6:157941654
|
G | T | 32 | a0001c0001t0005g0295a0001c0003t0003g0203a0001c0003t0003g0251others(29): Show | 32 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1740+680G>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941654 | ||||||
| chr6:157941782
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1740+808T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941782 | ||||||
| chr6:157941791
|
T | C | 1 | a0002c0002t0002g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1740+817T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941791 | ||||||
| chr6:157941884
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1741-907G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941884 | ||||||
| chr6:157941893
|
A | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741-898A>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941893 | ||||||
| chr6:157941918
|
C | T | 2 | a0001c0001t0011g0060a0001c0001t0011g0259 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1741-873C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157941918 | ||||||
| chr6:157942032
|
G | C | 6 | a0002c0002t0002g0044a0002c0002t0002g0045a0002c0002t0002g0046others(3): Show | 6 | HG00280.hp1 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741-759G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942032 | ||||||
| chr6:157942065
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1741-726G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942065 | ||||||
| chr6:157942115
|
C | T | 13 | a0001c0003t0003g0263a0001c0003t0003g0264a0001c0003t0003g0265others(10): Show | 13 | HG01891.hp1 HG02602.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1741-676C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942115 | ||||||
| chr6:157942262
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741-529T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942262 | ||||||
| chr6:157942314
|
C | G | 1 | a0001c0003t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1741-477C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942314 | ||||||
| chr6:157942343
|
G | A | 1 | a0001c0001t0010g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1741-448G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942343 | ||||||
| chr6:157942367
|
C | G | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741-424C>G | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942367 | ||||||
| chr6:157942450
|
G | C | 18 | a0001c0001t0005g0295a0001c0003t0003g0203a0001c0003t0003g0251others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1741-341G>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942450 | ||||||
| chr6:157942570
|
G | A | 59 | a0001c0001t0006g0097a0001c0009t0006g0058a0002c0002t0002g0001others(56): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1741-221G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942570 | ||||||
| chr6:157942595
|
G | A | 6 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(3): Show | 6 | HG02055.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741-196G>A | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942595 | ||||||
| chr6:157942615
|
T | C | 106 | a0001c0001t0001g0248a0001c0001t0003g0250a0001c0001t0003g0257others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1741-176T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942615 | ||||||
| chr6:157942685
|
T | C | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741-106T>C | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942685 | ||||||
| chr6:157942731
|
C | T | 1 | a0001c0001t0013g0298 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1741-60C>T | SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 17/17 | chr6 | 157942731 |